3. Discussion
During your MRCP PACES examination, your examiners may give you
clues and tell you that this gentleman has problems with his speech.
If they give you clues that patient has problems with speech, I will
examine the patient's lower cranial nerves first.
Anyway, even though you have the habit for examining cranial nerves
from the every first to the last, you would notice that this gentleman has
very obvious wasting of the tongue.
4. If you remember from your old medical school time, muscles of the tongue
are supplied by hypoglossal nerve ( XII cranial nerve).
You must look for other cranial nerves involvment in this gentleman.
Further examination in this gentleman reveals that:
5. He has fasciculations of the tongue,
Vagus nerve(X) involvement as evidenced by weakness of soft palate
Nasal speech.
At this point, there are two important differential diagnosis, patients with Motor
Neuron Disease can present with either bulbar or pseudobulbar palsy.
Although patients with Guillain-Barre syndrome may give rise to similar
picture ( weakness of tongue with nasal speech), you must remember that
wasting is not obvious ( due to short duration of weakness in Guillain Barre
syndrome) and you may find ocular muscles involvement (Ophtalmoplegia)
especially in Miller-Fisher variant
Another important differential is Syringomyelia because it can involve lower
cranial nerves. Therefore, you must suggest to examiners that you would
like to examine your patient hands for any fasciculations or dissociated
sensory loss in order to differentiate these two conditions.
6. Common questions examiners would ask you
2) What investigations you would like to order in this gentleman?
Electromyography- shows widespread anterior horn cell damage. You
may want to do MRI to exclude other spinal cord or root compression
1) How do you differentiate bulbar from pseudobulbar palsy?
You can find the answers in any medical text book, however, I think the
tongue gives you good clues in differentiating these two (conditions)
3) What are the clinical patterns of motor neuron disease?
(
Bulbar, Progressive muscular atrophy and Amyotrophic lateral sclerosis
)
4) Who is the famous scientist in UK having motor neuron disease?
Of course, the most famous motor neuron disease patient is Professor
Stephen Hawking
9. Discussion
OK, examiners give you two clues here, patient is diabetic and female.
Yes, Necrobiosis Lipoidica Diabeticorum is common among female
diabetic patients.
Necrobiosis Lipoidica Diabeticorum is a disorder of collagen
degeneration with a granulomatous response, thickening of blood vessel
walls, and fat deposition. You must always suggest to examiners that you
would like to look for similar lesions over pre-tibial area ( a classical
location), scalp, trunk and upper extremities. Suggest to exaimers as
well that you would like to check urine for glucose.
Classically it is decribed as well-circumscribed papules or nodules that
expand with an active border to become waxy, atrophic, round plaques
centrally. Initially, these plaques are red-brown in color but progressively
become more yellow and atrophic in appearance.
10. Common questions examiners would ask you
1)What is the histology of this lesion?
Histopathologically, it presents with interstitial and
palisaded granulomas that involve the subcutaneous
tissue and dermis.
2)What is your differential diagnosis?
Sarcoidosis of the skin!
13. Discussion
There are different possible questions that can be asked in the
examination besides the above question, other possibilities include:
Look and proceed!
Would you like to examine this patient's thyroid status.
This lady complains of tremor, would you like to examine her.etc.
It is important for you to know how to approach this type of case, if the
question starts as assess this lady's thyroid status.I would most
probably start off by showing the examiners how I assess her thyroid
function by checking tremor, pulse rate, sweaty palm, thyroid eye
signs, opthalmoplegia and reflexes.
However, always remember to check for retrosternal extension, thyroid
bruit , proximal myopathy and pretibial myxodema
Then I would proceed to examine her thyroid gland and give a brief
description about the gland.
14. Conclusion
This lady has Grave's disease with diffused goitre and in a
hyperthyroid state.
Extra points
1) For Grave's opthalmoplegia, the first muscle to be involved is
inferior rectus.
2) Radio-iodine treatment can worsen Grave's eye disease.
3) Remember precautions to be taken after radioiodine treatment
16. Discussion
Usually this case is popular in skin sub-station at station 5.
Although it is rather uncommon in UK, SLE is endemic in South East Asia.
1- pattern of distribution of the rash
2- presence/absence of telangiectasia
3- any vasculitic rash
4- Any signs to suggest patient is on long term steroid therapy.
Suggest to examiners that you would do a complete physical examination to
look for other systems involvement. Always remember to check the patient's
BP, fundoscopy for cytoid body, urine for proteinuria and ask for drugs
history.
It is a common case especially if you are sitting your MRCP PACES in
Malaysia ,Hong Kong or Singapore. Always remember to present the
following
17. Conclusion
This lady has active SLE with malar rash and was admitted
due to joints pain.
Extra points
1-Remember in drug-induced SLE patients, their anti-histon
antibody is positive. Three common drugs that lead to drug
induced SLE are hydralazine, procainamide and isoniazide.
2- Drug induced SLE never involves brain and kidney.
19. Discussion
It is a gift if you get this case in your MRCP PACES, an important
sentence you must include in your presentation is bilateral, symmetrical
deforming polyarthropathy involving the small joints of hands especially
over PIP and MCP joints.
Always assess their functional status. Suggest to examiners that you
would like to examine other joints, look for splenomegaly ( Felty's
syndrome) and lower lobe fibrosis
Psoriatic athropathy may present with similar deformity but look hard for
other clues such as nail pitting, skin lesion and telescoping of fingers.
Always look hard for Cushing's syndrome although patients with RA are
usually not on long term high dose steroid.
20. Common questions they will ask in exams are:
1- Causes of anaemia in RA patients
2- Newer therapies available for RA
3- Mechanism for each joint deformity.
(Distinction question!)
21. Conclusion
This lady has RA and is on Methotraxate, salazopyrine and low
dose prednisolone
Extra points
Simple functional status you can assess in exam includes pincer grip
( ask patient to hold a key), functions of hands (unbuttoning of cloths)
and shoulder involvement ( comb the hairs).
Always look hard for other associated autoimmune disease namely
Sjogren's syndrome, autoimmune hepatitis etc.
22. 6-You are the SHO in charge of Infectious Disease Clinic
Subject: Mr Lee, 55 years old
Mr Lee is 55 years old chronic Hepatitis B carrier comes to your hospital for
right hypochondrium pain for 1 month. He was previously under his GP
follow up for his Hepatitis B infection. Yearly alfa-fetoprotein and ultrasound
abdomen are done for him and he was told to be normal.
Further CT abdomen and thorax in your hospital show that he has an
advanced hepatoma with lung metastasis. Your consultant has reviewed
the films and think there is no curative management for him.
Your task is to break the bad news to him and tell him there is only palliative
management available.
23. Discussion
It is rather a common question in MRCP PACES, breaking bad news is
always a popular question. There are usually two scenarios in this type
of question.
The first scenario will be breaking bad news to patients who are suffering
from chronic illnesses examples are patients with:
SLE
Motor neuron disease
Multiple sclerosis
Parkinson's disease
dementia etc.
Another scenario will be breaking bad news to patients with advanced
cancer.
24. It is more tricky in the first scenario because you are expected to know
fairly well the management of each illness, therefore you need to have
some theories basic to score in this type of question.
In this case , you must always anticipate that Mr Lee would ask you why
he is having hepatoma (Liver cancer) since all the while his GP tells him
that the tests are normal.
Whereas in the second scenario, you do not need to know anything about
the management of the advanced cancer, you can even score a four
without explaining anything about the management.
25. Common questions patient is going to ask you are:
1- Am I going to die, doctor?
2- Are you sure about the result, doctor?
3- I don't want to die, doctor, can you do anything to help me?
4- I don't want to tell my family, can you keep this as a secret?
5- Is there any other alternative treatment available?
27. Discussion
If you see bilateral ptosis in your MRCP PACES, then the examiners are
either going to give you a clear pass or a clear fail The reason is simple,
you can either give a clear diagnosis or you do not have any ideas.
You can make a diagnosis of dystrophia myotonica (DM) after you shake
the patient's hand. Patients with DM will have difficulty to release his/her
hand grip.
There are only two possibilities in MRCP, either you are dealing with
dystrophia myotonica or myasthenia gravis.
You can further demonstrate this by doing a percussion test. You can use
your tendon hammer to percuss at patient's thenar eminence , what you
notice will be flexion of the thumb and then slow extension of patient's
thumb.
28. To make a diagnosis of myasthenia gravis (MG), the most important
physical sign you need to demonstrate is fatiguability.
The morale of the story is , in neurology station always SHAKE YOUR
PATIENT'S HANDS BEFORE YOU PROCEED.
The next thing is you need to do is general inspection. If patient has DM,
you will pick up by noticing that there is frontal baldness, expressionless
face ( wasting of temporalis, masseters and sternomastoids) and bilateral
ptosis.
There are two ways to do this, one is asking patient to look upward and
start counting. You will notice patient will have difficulty to sustain upward
gaze and the speech becomes nasal. Another way is asking patient to do
repeated flexion and extension of shoulder.
29. Conclusion
This lady has ocular myasthenia.
Extra points
1- Remember a few examples of drugs that can precipitate
myasthenia crisis.
2- Remember the mode of inheritance of DM- autosomal dominant
and other associated symptoms and signs.such as cataract, diabetes,
and possible of heart block
32. Discussion
very common short station case in UK. What you notice here is multiple
telangiectasia over patient's face as well as over his ear lobe. Other
common sites to look for this are tongue, palate, nasal mucosa, nail
beds, arms and trunk.
After this, you should look hard for features to suggest heart failure if
there is possibility of presence of shunt. Try to auscultate for bruit over
the patient's lung and liver.
Last but not least, ask for family history because it is inherited in an
autosomal dominant way
Also check for anemia because patient tends to have PR bleeding.
Suggest to examiners you would examine fundoscopy to look for retinal
haemorrahage and do PR to look for bleeding.
33. Conclusion
This gentleman has hereditary haemorrhagic
telangiectasia ( Rendu-Osler-Weber Disease). He has
history of recurrent PR bleeding.
Extra points
1- Remember the simple management about this condition such as
oestogen, cauterization etc.
2- Remember in your management, one very important part is counseling
especially patient plans to have children in future.
34. 9-You are the SHO in charge of the medical clinic
Dear Dr
Ref: Mr Lee, 24 years old
Kindly see Mr Lee who complains of weight loss for the past 3
months. He had recently had a bout of chicken pox. This did
affect his lungs and I treated him for a chest infection with a
course of antibiotics. My main concern is that he still complains
of intermittent fevers and breathlessness
Please see and advise
With best wishes
Dr Oh Pee Dee
You have 14min until the patient leaves the room, followed by 1min for
reflection before the discussion with the examiners. Be prepared to
discuss the solutions to the problems posed by the case and how you
might reply the GP’s letter
35. Discussion
This question came out a few years back in Singapore MRCP PACES
examination. I want to show you this question to remind you that in your
examination, no matter what the patient's symptoms are, if the patient is
young, always think of HIV
You must not be judgemental about patient's sexual orientation and inform
patients that you are there to help him/her. My friend failed this station
because he failed to find out that this patient is actually a homosexual and
was practicing unprotected sex with a lot of partners. The diagnosis was
HIV with PCP
My friend who sat for the exam asked patient a lot of questions and covered
most of the possible diagnosis like thyrotoxicosis, inflammatory bowel
disease etc. However, patient refused to talk about his sexual encounters
when asked, a common scenario in PACES
Remember to convince the patient that it is important for you to take this
piece of information and you certainly share with him/her the feeling of
embarassment he/she may have
37. Discussion
It is a common case in MRCP station 5 of endocrine sub- station
There is presence of obvious purplish striae over his abdomen as well as his upper
thigh
Check for other obvious clinical signs such as buffalo hump, moon face, thin skin,
multiple bruises especially over venesection site, hirsutism and acne. Look for
proximal myopathy and spine tenderness.
Suggest to examiners that you would like to do the following, check the urine for
glycouria, check this patient's BP and ask relevant history to assess whether the
patient is on long term steroid. Look at his abdomen to see any surgical scar.
38. Conclusion
This gentleman has Cushing's syndrome secondary to long term
steroid ingestion ( from traditional medicine).
He was admitted due to fulminant sepsis with Addisonian crisis
Extra points:
1- Common diseases that requires patients on long term steroid are as
asthma, myasthenia gravis, nephrotic syndrome and other
autoimmune diseases.
2- Cushing's disease is always a common case in exam, remember
that besides making the diagnosis of Cushing, you need to find out the
underlying cause if possible and possible complications.
39. 11-You are the SHO in charge of the medical
clinic
Dear Dr
Mrs Lydia David, a 70-year old retired teacher comes to
your clinic because of jerky movement of her right hand for the
past four months. She has previous history of Diabetes Mellitus
on oral medications under her GP follow up. After a careful
physical examination and complete investigations, your
consultant neurologist thinks that Mrs Davis is suffering from
Parkinson's disease. Mrs David is in the clinic waiting to see you
for the investigation results and the diagnosis. You are the SHO
in charge of the neurology clinic, your task is to explain to Mrs
David about the diagnosis and answer her queries.
You have 14min until the patient leaves the room, followed by 1min for
reflection before the discussion with the examiners. Be prepared to
discuss the solutions to the problems posed by the case and how you
might reply the GP's letter.
40. Conclusion
This is a classical question that can be asked in your counselling station. I
call this type of question,Disease explanation question, other diseases that
are common in the exam include Alzheimer's disease, Motor neuron
disease, Hepatitis B and C , polycystic kidney disease etc.
1-to explain the illness in layman's terms
Usually all these diseases are chronic or they have a lot of social
implications. In this case, since that Mrs Davis is suffering from Parkinson's
disease, candidates are expected to do the following.
2-explain the prognosis and the likely progression of the illness
3-treatment for the disease- medical or any new treatment available such
as surgical intervention
4-ask social history especially the impact of the illness towards patient's
daily activities as well as patient's relationship with other family members
41. Extra points
The commonest mistake candidates make in this type of
question is trying to explain as much as possible about a
illness and not answering patient's queries about the illness
Try to give a lot of details about the illness and not bother
about the illness social implication.This gives an impression
to the examiners that you are not holistic in your approach.
43. Discussion
Ptosis is always a popular question in MRCP PACES, this
gentleman has left unilateral partial ptosis.
After you notice this, there are two common possibilities, either
the patient is suffering from left Horner's syndrome or left third
nerve palsy.
The second step you would like to do is of course to look at the
affected eye's pupil size. This will tell you whether you are
dealing with a third nerve palsy or Horner's syndrome.
If the pupil's size is small then you are dealing with Horner's or
else you are dealing with third nerve palsy especially you
notice that the eye is abducted
44. The subsequent relevant physical examination depends on your second
step finding, if it is Horner's syndrome, then you must find out the
underlying cause for this, the common sites to look for are patient's neck
( any cervical lymph nodes, mass?) , lung ( Pancost's tumour/ lung
cancer) or cervical spine ( syringomyelia- patient may have small muscle
wasting of hands).
If you are dealing with third nerve palsy, look for other cranial nerves
involvement, if there is only isolated third nerve palsy, then you are most
probably dealing with diabetes mellitus.
Isolated third nerve palsy can be a medical or surgical third nerve, if there is
pupillary sparing ( the pupil is normal size), then you are dealing with
medical third nerve palsy ( such as due to DM, hypertension), if the pupil
size also involved, then it is a surgical third nerve palsy ( such as due to
aneurysm compression).
45. Conclusion
This patient has left isolated third nerve palsy due to diabetes mellitus
Extra points
Common question examiners will ask you is the reason
behind pupillary sparing in medical third nerve palsy.
Sometimes (rarely) you may think that the patient has ptosis
but what the patient is having is unilateral proptosis due to
retroorbital tumour/ mass
47. Discussion
It is sometimes rather difficult for you to differentiate panhypopituaitarism
from hypothyroidism.
.
Always remember to look for cerebellar signs which is bilateral in
hypothyroidism. Also look for other associated endocrine involvement
such as DM, Addison's disease, Pernicious anemia and vitiligo.
However, if you look at patient's sexual characteristics, they are lost in
panhypopituitarism
Patients with hypothyroidism also tend to be older because the main
cause for panhypopituitarism is mainly due to Seehan's syndrome and
skull radiation which is commoner among younger patients
Suggest to examiners you would like to check for sensory deafness
especially to high tone. Try to find out the underlying cause for the
hypothyroidism if possible.
48. Conclusion
This lady has hypothyroidism secondary to previous total
thyroidectomy.
Extra points
1-Although it is rather uncommon in PACES, you can find this illness
rather common especially among older population. Always check their
thyroid status if an elderly patient presents to you with dementia
2-The commonest cause for hypothyroidism is previous total
thyroidectomy
51. Discussion
As discussed in previous issues, Cushing's syndrome is a popular
question in MRCP PACES, this lady has a classical moon-like facies.
You must look for other relevant clinical signs such as buffalo hump,
hirsutism, suprclavicular fat pad.
If you look hard, this lady has multiple vasculitic rash over her hands.
Look for purplish striae, proximal myopathy, spine tenderness and suggest
to examiners that you would like to check for BP, urine for glucose and
visual field.
it is rather uncommon for patient to have Cushing's disease and bitemporal
hemianopia because in Cushing's disease ,the tumour is usually a
mircoadenoma.
52. In MRCP examination, it is not enough for you to get the diagnosis of
Cushing's syndrome only. In view of the vasculitic rash over her hands,
you must look for other clues to suggest the possible underlying
diagnosis for this lady that leads her to be on long-term steroid.
The commonest cause for vasculitic rash is autoimmune disease and this
lady is actually having lupus nephritis and on long-term steroid. Suggest to
examiners that you want to look for other signs of lupus.
Common causes of Cushing's syndrome include
long term steroid ingestion (iatrogenic)
pituitary adenoma (Cushing's disease)
adrenal adenoma
adrenal carcinoma
and ectopic ACTH production (usually lung CA).
53. Conclusion
This lady has Cushing's syndrome secondary to long
term steroid ingestion due to lupus nephritis.
Extra points
Tests to confirm the presence of Cushing's syndrome are 24-hour
urinary free cortisol and overnight dexamethasone test.
Further tests to find out the underlying etiology include plasma ACTH
level, high dose dexamethasone test, CXR, ultrasound/CT abdomen and
sometimes inferior petrosal sinus sampling for ACTH level.
55. Discussion
A common finding in a patient with transplanted kidney but always
missed by candidates.
Actually this gentleman develops gum hypertrophy due to cyclosporin.
This gentleman has a superficial right lumbar mass with a scar. The
mass is dull on percussion and there is an AVF over his right wrist.
There is no ballotable kidney.
A lot of candidates pick up the clinical signs of a transplanted kidney but
unfortunately majority of them do not examine further to look hard for side
effects of long term immunosuppressants such as signs of Cushing’s
syndrome ( due to prednisolone), fine tremor, gum hypertrophy,
hypertension (BP), diabetes (urine for sugar) and hypertrichosis (such as in
this case) due to cyclosporin and jaundice ( side effect of Azathioprine ).
56. A common question examiners would ask you is ways for you to assess
whether the transplanted kidney is functioning well or not, you can suggest
the following:
look at the patient's 24-hours urine volume, good volume suggests good
function
tell examiners whether the transplanted kidney is tender on palpation, if not
tender most probably it is functioning well,( although current
immunosuppresants make this unlikely to happen even patients have
rejection, this sign is a classical sign we were taught in medical school long
time ago!)
auscultate for renal bruit at the transplanted kidney, long term complication
of a transplanted kidney is artery stenosis
look for any recent punctum wound at the AVF, if no recent wound, this implies that
patient is not dependent on haemodialysis, therefore the transplanted kidney must
be functioning well.
57. Conclusion
This gentleman has a transplanted kidney and on cyclosporin,
predisolone and azathioprine and he develops gum hypertrophy,
hypertension due to the drugs.
Extra points:
Common side-effects and precautions for immunosuppresants are as
follows:
Cyclosporine- nephrotoxity, hypertension, tremor, gum hypertrophy,
hyperuricemia, hyperkalemia, weight gain, diabetes mellitus, acne,
hypomagnesaeimia. Grapefruit juice and Mediterranean oranges and Sun
Drop, a citrus soda, contain bergamottin which enhances the effect of
cyclosporine, increasing the level of the drug in circulation.St John's wort
reduces the concentration of cyclosporine rendering it less effective
58. Azathioprine- bone marrow suppression, cholestatic jaundice, GIT upset.
Azathioprine can cause irreversible bone marrow failure for those with a
particular polymorphism of the TPMT gene. GlaxoSmithKline has a
predictive DNA test for this type of problem.
Prednisolone- Cushing's syndrome and its complications.
Mychophenolate-GIT upset, headache, bone marrow suppression.
Other common causes of gum hypertrophy include acute myeloid leukemia,
scurvy, medications such as cyclosporine, calcium channel blocker
especially nifidipine and phenytoin.
60. Discussion
In MRCP exam, if you encounter a surgical scar, it is always a good start
because surgical scar can give you a lot of clues that lead to possible
underlying diagnosis.
This lady has a roof-top scar ( can be just a horizontal scar at left lumbar
region) and further examination reveals jaundice, moderate hepatomegaly
but no stigmata of chronic liver disease ( always look for stigmata of
chronic liver disease, due to her illness , she needs multiple transfusions
and tend to get Hepatitis B and C in long run and possibility of liver
cirrhosis due to iron overload).
Look hard for any multiple small scars at the abdomen due to
subcutaneous infusion of iron-chelation therapy.The underlying diagnosis
for this lady with chronic haemolysis is Thalassemia with previous
splenectomy.
61. Although Thalassemia is rather uncommon in UK, it is common in Asia
especially if you are sitting your exam in Singapore, Hong Kong and
Malaysia. Suggest to examiners you would.
Examine for secondary sexual characteristics (any hypogonadism) because
there is possibility of delayed puberty due to iron overload
Check for patient’s height due to growth retardation secondary of iron
deposition at the pituitary gland
Check urine for diabetes mellitus
Look for signs of hypothyroidism (all these are due to iron overload)
Ask the patient any family history of anemia and Haemoglobinpathy.
There are in various occasions my friends got a abdominal case of isolated
mild splenomegaly and tinge of jaundice without hepatomegaly in their
MRCP PACES, always remember one of the most important causes is
chronic haemolysis ( although book always tells you that you tend to get
hepatomegaly as well, but I notice Thalassemia intermedia patients tend to
get splenomegaly ONLY).
62. Conclusion
This lady has Thalassemia Major and underwent a splenectomy due to
recurrent, frequent transfusions.
Extra points
a)Splenectomy should be considered if,
annual blood requirements exceed 1.5 times those of spenectomised
patients, provided they are on the same transfusion scheme and have no
other reasons for increased consumption.
Splenic enlargement is accompanied by symptoms such as left upper quadrant
pain and early satiety.
Leucopenia or thrombocytopenia due to hypersplenism.
63. b) Complications of splenectomy include peri-operative complications
such as bleeding,atalectasis and subphrnic abscess, long term
complications include thrombocytosis and overwhelming sepsis especially
to encapsulated organisms such as Streptococcus pneumonia,
Haemophilus influenzae and Neiserria meningitides.
c) Preventive measures a physician can utilize to prevent
postsplenectomy sepsis include immunoprophylaxis ( vaccination to
S.pneumonia, H.influenzae and N.meninngitidis), chemoprophylaxis (
oral penicillin) and patient education (explain about potential travel-
related infections)
64. 17-You are the SHO in charge of the medical unit.
Dear Dr
Ref: Mr David Letterman, 56 years old
Thank you for seeing Mr Letterman who complains of lethargy for the past
3 months. I have done a few investigations that turned out to be negative.
He has previous history of gastritis and claimed that OGDS done about 5
years ago showed some erosions and he was put on some medications.
He has history of Diabetes Mellitus for the past 10 years currently on T
Daonil 5mg bd. He is worried about his symptoms but unfortunately I can’t
find anything wrong with him.
Kindly see him and advise
With best wishes
Dr GP
You have 14min until the patient leaves the room, followed by 1min for
reflection before the discussion with the examiners. Be prepared to discuss
the solutions to the problems posed by the case and how you might reply
the GP’s letter.
65. Discussion
You must always think of possible differential diagnosis before you enter the
examination room. Mr Letterman complains of lethargy, a very vague
symptom. You must start off by asking him what does he mean by lethargy
Common causes of lethargy/tiredness can be due to anemia,
hypothyroidism, depression, myathenia gravis, obstructive sleep apnoea
You must ask him to explain his symptom. Some patients may associate
shortness of breath with lethargy. In whatever symptoms you are going to
encounter in MRCP PACES,always try to include these questions in your
history-taking if possible
any specific time the symptom becomes worse? If the patient is having
mysthenia gravis, he may tell you that he fells more tired especially during
evening
66. any precipitating or relieving factors ?
any other associated symptoms ?
In this case, you must ask certain questions which are specific for
hypothyroidism such as constipation, weight gain, cold intolerance
You need to rule out causes of anemia as well since that this gentleman
had a history of gastritis before. Ask about any symtoms to suggest blood
loss or symptoms to suggest malignancy
Depression is always a differential in your history taking, try to assess his
social history and symptoms to suggest depression
In obstructive sleep apnoe, patient may have snoring, early morning
headache and sleepiness during day time
As I mentioned earlier, myathenia gravis patients always tell you that their
symptoms worsen towards the evening
67. About his diabetes, you must always ask the following
his usual control, whether he has monitoring at home to monitor his sugar
possible complications such as IHD, retinopathy, peripheral neuropathy,
nephropathy ,TIA, stroke etc
Later, ask other relevant past history, such as in this case, ask the patient about
his OGDS and his symptoms
Last but not least, always assess patient's main concern, he may have some hidden
agendas that he like to tell you.
Actually, my friend had this case in his MRCP PACES in 2005, the
diagnosis was depression. My friend totally forgot to ask the patient about
his social history
This patient actually just lost his wife in a motor vehicle accident and he had very
poor social support and he developed depression after the incident!
69. Discussion
You may be panic when you first look at her hands. Always remember the
general rules for a good physical examination for locomotor system, i.e
inspect, feel, palpate, passive movement, functional assessment and
special steps! Always remember that NEVER SHAKE HAND WITH
PATIENT in locomotor substation.
but for neurology station, always do this first
You may cause pain to patient and examiners have 1 thousand and 1
reason to fail you! Always ask you patient whether he/she has any pain
over any specific joint, then I would ask them to rest their hands on a
pillow.
Second rule is proper exposure, preferably I would ask patient to expose
the whole upper limbs up to shoulder, the reason is simple, you do not
want to miss any skin rash ( especially psoriasis patch) , any skin nodule
(especially subcutaneous nodule over the elbow in rheumatoid arthritis )
and any abnormal joint deformity.
70. Describe any abnormality you can see such as joint deformity, muscles
wasting … etc. Do a proper inspection! What I mean, look over patient’s
palm as well as the back of the hand. If you do so
Ops……, the diagnosis becomes obvious after turning the patient’s hand
71. Another important inspection I would pay attention to is whether there is
presence of nail pitting. After general inspection, then feel the patient’s skin
gently to assessment whether there is presence of warmness that might
suggest disease activity.
Then palpate the patient’s joints by gentle passive movement and look for
any thickening of synovium or joint tenderness. Also try to feel for
calcinosis that might be present in scleroderma I would always tap at
patient’s flexor retinaculum to check for carpal tunnel syndrome
The last step is assessing patient’s functional status. Do at least these
three important steps, unbuttoning of clothes, pincer grip ( holding key)
and writing. If you suspect there is involvement of elbow and shoulder
joints, then ask patient to comb his/her hair. You can kill two birds with one
stone by asking patient to do so
You are going to assess patient’s elbow as well as shoulder joints. Then
the last step will be special steps depending on your findings. Such as in
this case, I would suggest to examiners that I would look for other joints
involvement and other common sites for psoriasis.
72. Common questions examiners would ask you
Why in arthritis mutilans, there is shortening of the fingers?
due to marked periarticular osteolysis and erosion
What is ‘pencil in a cup’ appearance in xray ?
Where are the common sites to find psoriatic patches ?
How would you manage psoriatic arthropathy
73. Conclusion
This lady has psoriatic arthropathy.
Extra points
Five types of psoriatic athropathy namely
oligoarticular asymmetrical type (70%)
distal interphalangeal type
rheumatoid arthritis-like ( common in exam because want to confuse you!)
ankylosing spondylitis- like
and arthritis mutilans
There are five types of psoriasis. They are chronic plaque, inverse
psoriasis, pustular, guttate and erythrodermic types.
Facts from Baliga's book!
76. Discussion
Patients with scars again I want to show you this case for a simple reason.
There are only a few common causes of a sternotomy scar in CVS station.
These causes include previous bypass surgery, valve replacement and
correction of congenital heart diseases such as VSD ( ventricular septal
defect) and ASD ( atrial septal defect )
At the first look, you might think that these patient has had a bypass surgery
before due to the scar over his leg.
The problem is he actually has a bypass and aortic valve replacement
(AVR) surgery done before.
Lesson to be learned here is always look for concomitant AVR if patient has
had a bypass before especially in elderly population because aortic stenosis
is common among this age group
During your examination, always look hard for any bruises to suggest over-
warfarinization, signs to suggest endocarditis and murmurs to suggest valve
dysfunction
77. Common questions examiners would ask you
Complications of mechanical prosthetic valve
can be divided into complications due to the valve itself such as dysfunction
haemolysis, endocarditis
and complications due to the treatment because of warfarin
Causes of anemia in a patient with prosthetic valve.
How to differentiate a tilting disc valve from a ball cage valve clinically?
(distinction question!)
How to assess whether the valve is functioning well clinically?
78. Conclusion
This gentleman has AVR surgery done before due to previous
aortic stenosis and bypass surgery.
Extra points
You can’t find any donor site and no mechanical click when you
examine the patient but you see a sternotomy scar, you might be
dealing with previous corrective surgery due to congenital heart or a
BIO-PROSTHETIC VALVE
Although patients with valve repairs tend to have left thoracotomy scar
( such as in mitral stenosis), I found out some patients may have
sternotomy scar!
80. Discussion
It is an uncommon case in MRCP, however, it is worthwhile to learn
about this
If you look carefully at her lower limbs, you actually notice this lady has
a reticular pigmented rash
There are two common scenarios in PACES that give reticular
pigmented rash. These two conditions are erythema ab igne and livedo
reticularis
.
It can be quite difficult to differentiate these two conditions, however,
erythema ab igne usually appear to be more dusky and besides over
the lower limbs, you can find it on the abdomen
81. It is uncommon to find erythema ab igne in tropical countries, therefore,
you shouldn't be too worried if you are going to sit your MRCP in
Singapore, Dubai or Malaysia
The reason is simple because it is associated with repeated exposure to
heat especially in the elderly who sit in front of open fireplaces.
You seldom need to sit in front of fireplaces to get heat in these countries
because of the weather.
Look for signs of hypothyroidism and tell the examiners you would look for
underlying malignancy such as intra-abdominal malignancy or chronic
pancreatitis
Whereas in livedo reticularis, it is associated with SLE and usually found
in young females
If you find livedo reticularis, always look for other signs to suggest SLE
and also tell examiners that you would look for underlying malignancy as
well
82. Common questions examiners would ask you
1- Can livedo reticularis be normal ?
Yes, because it can be found in young females especially in cold
weather
What other conditions are associated with livedo reticularis ?
Besides SLE, other conditions include polyarteritis nodosa, occult
malignancy and microemboli of skin.
83. Conclusion
This lady has livedo reticularis due to SLE
Extra points
1- Although it is not a popular question, livedo reticularis is often missed
by candidates in SLE patients during their exam
If you are dealing with a SLE patient, skin conditions that are
associated with SLE are hyperpigmentation, discoid rash, malar rash,
livedo reticularis, alopecia, purpura, telangiectasia and vasculitic rash.
2- If you find erythema ab igne in patient's lower limbs, always look at
the abdomen as well!
85. Discussion
This is a commoner question as compared to Q1 in MRCP exams
Yes, you are right, it is acanthosis nigricans! It is always described as
'black, velvety overgrowth in the skin' by books.
Always tell the examiners you would look at other sites for this especially
over the neck ( a very common site other than axilla, especially at the
back of the neck), umbilicus, nipples, groins and facial skin
Also suggest to examiners that you would:
check the urine for glycouria ( because patient may have insulin resistance )
check for occult malignancy especially adenocarcinoma of stomach
ask for menses irregularity if the patient is female because it is associated
with polycystic ovarian syndrome
86. Common questions examiners would ask you
1) What conditions are associated with acanthosis nigricans?
2) How do you define metabolic syndrome?
87. Conclusion
This gentleman has acanthosis nigricans and diabetes mellitus.
Extra points
Remember criteria to diagnose metabolic syndrome either based on
NCEP or WHO criteria.
Remember 1 or 2 examples of cutaneous manifestations of viceral
malignancy such as dermatomyositis and Paget's disease of the nipple
89. Discussion
A very popular question in MRCP PACES exams. This case can be
used as a case in skin as well as locomotor sub-stations
You notice that this lady has tight skin over her face with multiple
telangiectasia (arrows )
You can see clearly that her mouth appears to be tight.Demonstrate by
asking the patient to put 3 fingers into her mouth
Describe the nose and proceed to do the following
check for dry eye because Sjogren's syndrome can be associated with
scleroderma.
check the hands and look for sclerodactyly ( image next slide),
Raynaud's phenomenon, peudoclubbing and calcinosis.
Also assess the extent of skin involvement!
90. assess the patient's hands
functions by doing hand
grip, pincer grip (holding
key) and unbuttoning of
clothes.
ask patient relevant
history such as dysphagia,
shortness of breath (lung
fibrosis) and diarrhoe
(malabsorption )
ask permission from examiners that you would like to listen to her lungs,
check her BP ( ? hypertension), look for other organs involvement and look
at her stool for evidence of malabsorption.
91. Common questions examiners will ask you
what types of autoantibodies can be present ?
ANA,anticentromer and anti-topoisomerase
what are the prognostic factors ?
Sex- male tends to do worse, patients with extensive skin involvement
and renal involvement tend to do worse
How to explain chronic diarrhoe in this type of patient ?
bacterial overgrowth
What are the criteria to diagnose of scleroderma ?
How would you manage a patient with scleroderma ?
92. Conclusion
This lady has systemic sclerosis
Extra points
Prednisolone has no role in treating systemic sclerosis.
Four reasons for this type of patient to get anemia.
iron deficiency due to chronic oesophagitis
anemia due to malabsorption
anemia of chronic illness
and microangiopathic haemolytic anaemia.
94. Discussion
It is an easy case if you know how to approach this case
You can see obviouly two small swellings over this gentleman's first toe
and little toe.
Although books describe chronic tophaceous gout as 'chalky 'material,
sometimes you would just notice a swelling such as in this case.After
you feel, palpate and move the relevant joints, you should look at other
sites for similiar swelling.
These sites include helices of the ears, olecranon bursae, tendons of
hands and Achilles tendon.
Another diagnosis that you may confuse with swelling over tendons is
tendon xanthomata
Also suggest to examiners that you would look at the urine for
haematuria and you are very interested to know about this patient's
renal function.
95. Common questions examiners would ask you
What factors can precipitate acute gouthy arthritis ?
When do you start to treat hyperuricemia ?
How do you explain patients with gout to have bilateral leg swelling ?
Fluid overload due to CRF
96. Conclusion
This gentleman has chronic tophaceous gout.
Extra points
Clinical presentations of gout include asymptomatic hyperuricemia,
acute arthritis, chronic arthritis and chronic tophaceous gout.
Uric acid crystals are negatively birefringent.
98. Discussion
First lesson to be learned in abdominal examination is appropriate
proper exposure.
My friend failed this station because he insisted to expose his female
patient in his MRCP PACES exam down to thigh. I would expose the
patient up to just above the genitalia.
Obviously you notice this gentleman’s abdomen to be grossly
distended and there are multiple tattoos at his supra-pubic region.
You also notice presence of jaundice, ascites (shifting dullness),
clubbing and splenomegaly in this gentleman.
You must always remember that beside making a diagnosis of chronic
liver disease, you should try to find out the underlying cause for his
chronic liver disease.
99. some clues may help you.
If you find……..
parotid swelling
Dupuytren’s contracture – you may be dealing with alcoholism
skin hyperpigmentation- you may be dealing with
haemochromatosis or iron overload due to multiple transfusions in
Thalassemia patients (although you are unlikely to see this in UK,
you may be seeing this type of cases in developing countries)
tattoos or punctum wound to suggest intravenous drug abuse- you
may be dealing with Hepatitis B.
100. Common questions examiners will ask you
What is Child’s grading of liver disease in portal hypertension?
The mnemonic to remember BAPA + E
bilirubin, ascites, PT (INR) and albumin and encephalopathy
What are the possible complications of portal hypertension?
101. Conclusion
This gentleman has chronic liver disease due to
Hepatitis B ( He is an ex- intravenous drug abuser.)
Extra points
Remember that the commonest cause of chronic liver disease in Asia is
chronic viral hepatitis whereas in UK is alcoholism.
Do not forget that Wilson’s disease also can cause chronic liver
disease
102. 25-You are the SHO in charge of the Infectious
Disease clinic
You are asked by the sister in charge of the surgical ward to see Dr
Henry who accidentally pricks himself while taking blood from a HIV
patient in the ward. Dr Henry just started his internship 3 months ago
in the surgical department and he is very worried about this incident.
He is waiting to see you to discuss about post exposure prophylaxis
(PEP).
You task is to explain to him about post exposure prophylaxis.
You have 14min until the patient leaves the room, followed by 1min for
reflection before the discussion with the examiners.
103. Discussion
HIV is a very important topic in MRCP PACES exam. This is a common
scenario in station 4 for MRCP PACES.
Candidates should start off by expressing their empathy towards this
event.
Before going to the major task of any scenario in the exam, always
remember the following rules
ask about details of the event- in this case, you should ask Dr Henry
about the time of the event, size of needle he was using,
the depth of
needle penetration and what was his action after the incident
assess the patient’s understanding about certain issue, in this case, Dr
Henry’s understanding about HIV/AIDS
explain to Dr Henry the current problem/illness, in this case about
HIV/AIDS including the disease progression, modes of transmission
and possible treatment
104. assess Dr Henry’s risk to get certain infections such as HIV, Hepatitis B
and Hepatitis C. Ask him whether he knows about his status and his
previous Hepatitis B vaccination
ask more about that HIV patient’s status -? on treatment,?CD4 count, any
other medical problems such his ? Hepatitis B/ VDRL/ Hepatitis C status.
tell him you are there to help him and you certainly understand his feeling
right now, (always remember that the strategy in exam is ……… reassure
patient, reassure patient and keep on telling them you are there to help
everyway possible)
then inform Dr Henry briefly about PEP and maybe include some details
about the possible side effects. (Do not try to show off to examiners by
bombarding patient with very detailed information. This would make you to
score less point)
also inform Dr Henry about your plan for his follow up, do not forget to ask
his permission for HIV testing.
105. Actually in the real MRCP PACES, Dr Henry was just got married 4
months ago and he is very worried about his relationship with his wife
He is also worried whether he can continue to function as a houseman
while waiting for his blood results
You must always remember that patients in MRCP always have some
hidden agendas that they want to discuss with you
You may miss these issues if you do not ask them specifically
Last but not least, always ask patient whether they have any other
issue to discuss
106. Common questions examiners would ask you
What is ‘window period’ for HIV infection?
How do you decide what treatment to be offered to Dr Henry?
Extra points
PEP regime usually consists of combinations of three drugs
109. Discussion
You will be happy to see this case in your MRCP PACES. You can
get the diagnosis after your inspection
You notice that there are multiple distended veins over this
gentleman’s chest.
You can proceed with the usual physical examination of the
respiratory system by bearing in mind that you may find the following
abnormalities:
Pancoast’s tumour- you may find reduced breath sound over upper
lobe of the lung with dullness on percussion.
Pleural effusion at one side of the chest.
Or any physical sign suggesting presence of mass such as dullness
on percussion with reduced breath sound.
110. After your complete physical examination, do the following steps:
Demonstrate the direction of the venous flow.
Look for exophthalmos, conjunctival injection.
Look at the JVP( non-pulsatile) and show to examiners how you
measure it.
Examine the cervical region for lymph nodes.
Look for small muscles wasting of the hand and Horner’s syndrome if
you are suspecting Pancoast’t tumour.
Suggest to examiners you would like to demonstrate Pemberton’s
sign if possible.
Ask the patient about smoking history.
Talk to patient to assess hoarseness of voice.
111. Common questions examiners would ask you
What is Permberton’s sign?
What is para-neoplastic syndrome and give a few examples?
Name types of lung carcinoma.
What are the contraindications for surgical intervention?
112. Conclusion
This gentleman has superior vena cava obstruction due to lung
cancer.
Extra points
If possible, non small cell lung cancer should be treated with surgical
intervention. For small cell lung cancer, it should be treated with
chemotherapy.
Indications for radiotherapy include SVC obstruction, local obstruction
such as airway, spinal cord compression and brain metastasis.
114. Discussion
In MRCP PACES, after lower limbs examination and Parkinson’s
disease, upper limbs examination is the third most popular question.
You notice that there are obvious small muscles wasting with loss of
thenar and hypothenar eminences.
Before you proceed further, you should know that there are only a few
possible causes for this.
The causes are Motor Neuron Disease, Cervical Spondylosis,
Syringomyelia ,Charcot- Marie- Tooth and Guillain Barre Syndrome ( or
CIDP-chronic inflammatory demyelinating polyneuropathy ).
It is unlikely for you to get bilateral Ulnar nerve palsy in exam.
Therefore, during your examination, pay attention to assess whether
there is sensory involvement or presence of fasciculation ( which may
suggest Motor Neuron disease ).
115. After you upper limbs examination, suggest to examiners that you
would do a proper examination of lower limbs. Pay attention to the
following:
presence of pes cavus and 'inverted champagne bottles’ lower limbs.
This suggest Charcot -Marie- Tooth.
Dissociated sensory loss of lower limbs with upper motor signs. This
suggests syringomyelia.
Upper motor signs of lower limbs with possibility of sensory level. This
suggests cervical spondylosis.
Flaccid paralysis of lower limbs with no sensory involvement. This
may suggest Guillain Barre syndrome.
After the examination, suggest to examiners that you would look for
Horner’s syndrome if you suspect syringomyelia
116. Common questions examiners would ask you
What is the CSF finding in GB syndrome?
What are the three recognized forms of hereditary motor
sensory neuropathy?
117. Conclusion
This lady has CIDP
(due to the chronicity, she has muscles wasting).
Extra points
In MRCP PACES, you are unlikely to get a case of isolated ulnar ,
radial or median nerve palsy
There are three main clinical patterns of MND, they are progressive
muscular atrophy ( obvious small muscles wasting of hand) , Bulbar
palsy and amyotrophic lateral sclerosis.
119. Discussion
This is a classical case in MRCP PACES station 3. A lot of candidates
always feel very worried when faced with cranial nerves examination.
You notice that this gentleman has obvious loss of right naso-labial fold.
A lot of candidates always ask me the same question, should I examine
from the first cranial nerve till the 12th cranial nerve or examine the
nerves according to scenario?
I think that it is important for you to divide cranial nerves to 4 main sub-
groups, these groups are:
1-Eye group- you will be testing cranial nerves II, III, IV and VI. You will
be assessing these cranial nerves by checking eye reflexes, fundoscopy,
visual acuity, visual field and eye movement.
2-Facial expression, sensation and movement- you will be testing cranial
nerves V and VII. You must check for upper and lower portion of facial
expression, corneal reflex ,masseter and pterygoid movement.
120. 3-Articulation and gag reflex- You will be testing cranial nerves IX,X
and XII. Check these nerves by assessing palatal movement, gag
reflex and tongue movement.
4-Other groups- assess VIII nerve by checking hearing, XI nerves by
asking patient to lift the shoulders and the first nerve by assessing
smell.
In this case, since you notice this patient has problem mainly due to
facial expression and movement, I would examine his V and VII nerves
first.
You know that he has 7th nerve palsy, the next question you want to
ask is whether it is a lower or upper motor 7th nerve palsy.
You can differentiate this by observing 2 major upper portion facial
muscles namely orbicularis oculi and frontalis muscles.
121. Ask patient to screw his eyes and look upward
If you do this, you notice the following,
122. You notice that he is unable to close his right eye tightly as compare to
the left eye.
So the diagnosis is obvious now, you are dealing with right lower motor
7th nerve palsy.You can then complete other cranial nerves examination.
After your examination, you want to find the possible aetiology for his 7th
nerve palsy by doing the following steps:
1-look at external auditory canal for herpes zoster
2-palpate for parotid swelling
3-check for hyperacusis
4-examine the taste involvement ( anterior 2/3 )
5-test urine for glycouria
123. Common questions examiners would ask you
What are three components of facial nerve?
Why there is sapring of upper portion of facial muscles in upper motor
lesion of facial nerve?
How would manage Bell's palsy?
What are the common causes of lower motor facial nerve palsy?
124. Conclusion
This gentlema has right Bell's palsy.
Extra points
Bell's palsy should be treated with combination of steroid and acyclovir.
126. Discussion
In MRCP PACES, if you find clubbing in respiratory station, you are
dealing with only a few possibilities, the most popular question will be
bronchiectasis.
Other causes of clubbing because of respiratory system are Lung
Cancer, suppurative lung disease ( such as empyema, therefore you
would find signs suggesting pleural effusion, however, it is unlikely in
MRCP because patients tend to be very ill!) and fibrosing alveolitis.
A lot of candidates find it difficult to differentiate lung fibrosis from
bronchiectasis. I think there are a few important points to take note….
Patients with bronchiectasis tend to be more ill because they are
admitted to hospital because of lung infection.
127. Patients with bronchiectasis produce copious sputum, therefore,
always look at sputum cup.
Lung fibrosis patients may have other signs to suggest the underlying
cause such as Rheumatoid hands, scleroderma signs etc.Besides
that, they might have Cushing features due to long term steroid.
After the examination, suggest to examiners that you would like to
look at the temperature chart…
Crepitation in bronchiectasis is described as coarse and the quality
changes with coughing.
128. Common questions examiners would ask you
What are the causes of brochiectasis?
How would you manage this condition?
What are other causes of clubbing?
129. Conclusion
This gentleman has bronchiectasis due to previous tuberculosis.
In bronchiectasis , remember postural drainage, postural drainage,
postural drainage…
Extra points
If you find patient with bronchiectasis also has dextrocardia, the
diagnosis is Kartagener's syndrome
130. 30-This gentleman has difficulty in walking.
Examine his lower limbs neurologically.
131. Discussion
An uncommon case in your daily practice but it is suprisingly a popular
question in MRCP. Many candidates were asked to examine this case
in their PACES before.
I have friends who sat thier MRCP in Malaysia ( especially at University
Malaya Medical Centre), Singapore ( at National University Hospital)
and Hong Kong were asked about this case in their Neurology Station.
Obviously if you observe properly, you notice there is hypertrophy of
both calf muscles
Yes, you are dealing with PSEUDOHYPERTROPHY of calf muscle
132. further examination reviews that:
This gentleman has waddling gait.
His proximal muscles are weaker that his distal muscles.
His ankle and knee reflexes may be normal and there is no sensory
involvement.
After your complete neurological examination, do the following steps:
Demonstrate Gower's sign.
Suggest to examiners that you would examine the upper limbs and look
hard of upper limbs involvement as well. Look for pseudohypertrophy of
deltoid muscle also.
Demonstrate winging of scapula by asking patient to straighten his
elbow and push against resistance.
Suggest to examiners you would ask about family history of similar
problem.
Look for any surgical scar to suggest recent muscle biopsy.
133. Common questions examiners would ask you
Why do you say that it is pseudohypertrophy and not true hypertrophy
of calf muscle in this condition?
How do you differentiate Duchenne from Becker muscular dystrophy?
What is the inheritance pattern in this condition?
How do you investigate and manage this condition?
Remember GENETIC COUNSELLING
134. Conclusion
This gentleman has proximal myopathy due to Becker Muscular
Dystrophy.
Extra points
There are a lot of causes for proximal myopathy, however if you notice
pseudohypertrophy of calf or deltoid muscles, it is usually due to
Hereditary Muscular Dystrophy.
Other common cases of proximal myopathy in MRCP PACES are either
polymyositis or dermatomyositis.
136. Discussion
Another popular neurology case in MRCP PACES, there are a few
possibilities you are dealing with Pes Cavus in MRCP.
You may be asked to talk to a patient who has a Cerebellar ( staccato
and scanning speech) speech and find out that he/she has pes cavus
with Friedreich's ataxia.
Or there is another scenario where you are asked to examine a
patient's upper limbs and you find that he/she has small muscles
wasting of both hands and 'inverted champagne bottles' lower limbs
with pes cavus
Yes , you are dealing with Charcot-Marie-Tooth Disease.
137. The two commonest causes for Pes Cavus in MRCP are Friedreich's
ataxia and Charcot-Marie-Tooth Disease.
Your further steps of examination depend on your finding, if you
suspect Friedreich's ataxia after your lower limbs examination,
suggest to examiners that you would like to:
ask about family history
check fundoscopy to look for optic atrophy.
examine relevant cerebellar signs.
look for kyphoscoliosis
138. Common questions examiners would ask you
What is the mode of inheritance for Friedreich's
ataxia or Charcot Marie Tooth?
What is the pathogenesis of pes cavus?
139. Conclusion
This gentleman has pes cavus due to cerebral palsy.
Extra points
In MRCP PACES, if you are asked to examine lower limbs, always
look at the upper limbs as well and vice versa.
Remember that other causes of Pes Cavus are poliomyelitis and
muscular dystrophy.
141. Discussion
This is a very popular skin station in MRCP exam. A lot of candidates find it
difficult to describe skin lesion. I think there are a few important points you
must give to examiners when you try to describe any skin lesion.
Your description must include the general appearance of the lesion (either
it is a macule, papule, blister or bullous).
site of the lesion ( is the lesion only localised to certain areas such as
extensor surface, umbilicus, scalp, palm etc?)
any mucosal involvement ( do you notice any mucosal involvement such
as over oral cavity, eye?) , is the skin lesion itchy or tender and any
associated changes that you think is relevant ( any hand/nail or other
changes such as pitting of nail, rheumatoid hands,thyroid swelling which
might be relevant!) I find that it is rather important for candidates to have a
general inspection before zooming to the skin lesion.
142. Sometimes, when you are asked to examine a skin lesion over the leg,
look at patient's eye and thyroid swelling which might tell you the
diagnosis ( pretibial myxoedema).
Common skin problems over lower limbs which are popular in MRCP
exam are pretibial myxoedema, erythema nodusom, erythema
multiforme,pyoderma gangrenosum and psoriasis.
In this picture, you notice macular-papular rash over patient's lower limbs
but there is no mucosal involvement, you do not not notice any bullous
eruption. You should proceed to do the following:
feel the lesion to assess whether it is tender ?
look at patient's mucosal ( oral cavity to look for ulcer ) and
check for conjunctivitis.( mucosal involvement)
check for lymph nodes especially cervical region ( glandular
fever?) and ask for drug history.
143. Common questions examiners would ask you
1) What is Steven Johnson syndrome?
2) What is the difference between Steven Johnson syndrome
and toxic epidermal necrolysis?
3) If a patient had joint pain over ankle 3 weeks ago and was
prescribed a medication by GP,what is the possible medication
involved?
4) How do you manage this condition?
144. Conclusion
This lady has macular-papular rash due to drug allergy.
Extra points
1) Always remember that you are not expected to diagnose all
skin conditions, you would pass if you give a good and
comprehensive description about the skin lesion.
146. Discussion
I give you this example because I think this is a popular case in MRCP.
This case can be either come out in station 1 or station 5 (skin station)
.
If you notice xanthelasma in a middle-aged woman with jaundice in
your MRCP, always think of Primary Biliary Cirrhosis. You may find
stigmata of chronic liver disease in this type of patient with +/- of
hepatosplenomegaly.
As I mentioned in my previous posts, you can gather some clues from
peripheral to get the underlying cause of a patient's chronic liver
disease, xanthelasma is one of them.
Having said that, xanthelasma can be asked in station 5 as well.
Besides xanthelasma, other stigmata of high cholesterol level include
tendon xanthomata, eruptive xanthomata,palmar xanthomata and
corneal arcus.
147. Classification of hyperlipidemia is based on Fredrickson which
can be divided to Type I to Type V. After your examination, proceed
to the following:
look for other stigmata of hyperlipidemia
assess other risk factors for coronary heart disease
such as sugar in urine, blood pressure and smoking.
try to assess the possible secondary causes such as
look for urine protein ( nephrotic syndrome), signs to
suggest hypothyroidism.
family history of premature death due to coronary
heart diseas and hyperlipidemia.
148. Common questions examiners would ask you
1) How do you manage hyperlipidemia?
2) What are classes of drugs available to
manage high cholesterol?
149. Conclusion
This gentleman has xanthelasma with underlying Diabetes
Mellitus.
Extra points
1) Learn a few important clinical trials involving statin such as 4S,
MIRACL which are commonly asked in MRCP.
2) Remember the common side effects of statin.
151. Discussion
A very popular MRCP question in respiratory station. When you find
a lateral thoracotomy scar in respiratory station, always think of three
possibilities:
namely lobectomy, pneumonectomy and previous lung
transplantation surgery.
A lot of candidates remember the first two possibilities but always miss
the third. The reason is simple, doctors working in many countries such
as in Malaysia and Singapore do not deal with post lung transplant
patients so often as thier counterparts in developed country such as the
United Kingdom and Ireland .
Therefore, if you are planning to sit your MRCP PACES in United
Kingdom, learn well about transplantation.
152. When you see a lateral thoracotomy scar, spend a few seconds to
have a thorough look at your patient, if you notice physical signs
suggesting Cushing's syndrome, then you are most probably dealing
with a patient after lung transplantation.
Always pay attention to look for side effects of cyclosporin as well
such as gum hypertrophy and excessive hair growth.
If you do not notice these, then you are most probably dealing with
lobectomy or pneumonectomy, some candidates find it difficult to
distinguish these two conditions, I think there are a few important
points to take note.
First point, in lobectomy, you may find reduced breath sound in certain
areas such as upper/middle/lower region but in pneumonectomy,
there is reduced breath sound over the whole affected lung.
Second point, there may be no sign to suggest mediastinal shift in
lobectomy ( central trachea) but in penumonectomy, you are expected
to find signs suggesting mediastinal shift ( based on your tracheal
position or apex beat).
Third point, percussion would review dullness generally for
pneumonectomy but not in lobectomy.
153. Common questions examiners would ask you
1) What are the indications for pneumonectomy or lobectomy?
2) What are the common indications for lung transplant in United
Kingdom?
3) What are the common side effects of cyclosporin?
4) What are the contraindications for surgical intervention in lung
cancer?
154. Conclusion
This lady has lateral thoracotomy scar due to previous lobectomy
because of lung cancer.
Extra points
1) Always take your time to observe for any surgical scar in your
respiratory station. You may be able to diagnose the condition before
even touching the patient!
2) Lobectomy or even pneumonectomy was done previously for
treatment of tuberculosis!
156. Discussion
A rather uncommon case in your daily practice but it is popular in
MRCP cardiovascular station. You notice this lady has long fingers
(arachnodactyly).
Patient's hand is at the left and mine is over the right. You would be
happy if you get this case,yes, finally you are seeing a case of Marfan
syndrome in your exam.
Demonstrate to examiners and convince them that the patient's fingers
are long by demonstrating thumb sign ( ask patient to clench her
thumb in her fist, the thumb should not exceed the ulnar side of the
hand in normal subjects) and wrist sign ( put patient's fingers around
her wrist, you would notice her thumb and little finger overlap),
look for other signs to suggest Marfan syndrome such as high arched
palate ( in this patient), small papules in the neck, up-ward dislocation
of the lens, kyphoscoliosis, and chest wall deformity.
157. For the heart, you would
anticipate you are most
probably to find either
aortic regurgitation or
mitral regurgitation.
Remember to suggest to
examiners that you
would like to ask about
the family history .
158. Common questions examiners would ask you
1) What are the diagnostic criteria for Marfan syndrome?
2) What are the differentiating features between Marfan syndrome
and Homocyctinuria?
3) What is inheritance pattern for Marfan syndrome?
159. Conclusion
This lady has Marfan syndrome and mitral regurgitation .
Extra points
1) When asked about the management of an illness, always
remember that patient education is very important if the illness is
chronic and incurable. Remember genetic counselling if it is inherited.
2) Cardiovascular complications are the major cause of death in
Marfan syndrome!
161. Discussion
As I mentioned in my previous posts. You should score in your
abdominal station. This is because there are only very limited
possibilities in abdominal station.
You notice this gentleman has gynaecomastia as evidenced by
presence of breast tissue.Look for other stigmata of chronic liver
disease such as:
Clubbing-Dupuytren's contracture-palmar erythema-spider naevi-
flapping tremor-leukoonychia-scratch mark-jaundice-pallor-
pigmentation-cyanosis-xanthomata-purpura-koilonychia-paronychia-
oedema-muscle wastimg-tattoos-needle marks....( you would be
surprised to find that there are so many physical signs in chronic liver
disease!).
Although there are a lot of causes for gynaecomastia, if you find this in
your abdominal station, always think of chronic liver disease.
162. Remember that common drugs that are associated with gynaecomastia are
ketoconazole, spirolactone, H2 antagonist such as cimetidine and
psychoactive drugs.If you look at the periphery, you would find the
following,
Yes, you would notice that
this gentleman also has
leukonychia. Anticipate to
find hepatosplenomegaly in
this gentleman.
Demonstarte to examiners
that you know how to check
for ascites by showing
shifting dullness.
Showmanship is important
in MRCP clinical exam.
Always examine your
patient systematically and
confidently.
163. Common questions examiners would ask you
1) How would you investigate this patient?
2) What are the common trigerring factors for hepatic encephalopathy?
3) How do you diagnose spontaneous bacterial peritonitis?
4) What is your long term plan for liver cirrhosis patients?
164. Conclusion
This patient has chronic liver cirrhosis due to alcoholism.
Extra points
1) Currently there are a few drugs available for Hepatitis B treatment
besides intereferon. Learn about Lamivudine, adefovir and entecavir.
2) Learn more about CAGE questions when you want to get further alcohol
history from a patient! ( Study back your medical school book to learn more!)
167. Discussion
This is the continuation discussion from the previous issue. As I
mentiond in previous article, Marfan Syndrome is a popular cardiology
case in MRCP. However, this case can come out in Station 5 as well.
You notice that this lady fingers are long. I would like to show the thumb
and wrist signs as I mentioned in previous issue. Always remember that
for you to diagnose Marfan syndrome, you need to know about the
major criteria.
Major criteria for Marfan syndrome include Ectopia Lentis ( upward
dislocation of the len), dilatation of aortic root or aortic dissection and
lumbarsacral dural ectasia ( you only can diagnose this by MRI or CT
scan).
If patient has family history , you need two systems involvement ( either
skeletal system, ocular, cardiovascular or other system ) to diagnose
Marfan syndrome. If patient does not has family history,then you need
two systems involvement plus one major criteria!
168. Common questions examiners would ask you
1) How do you manage this condition?
( Remember about genetic counselling and patient's education)
2) What are common cardiovascular lesions in Marfan syndrome?
169. Conclusion
This lady has Marfan syndrome
Extra points
Remember the complications of Marfan syndrome!
171. Discussion
A very, very popular skin station in MRCP exam if you are taking the exam
in Malaysia or Singapore. You notice that this gentleman has multiple
angiofibroma (adenoma sebaceum) over his face ( malar distribution).
The diagnosis is clear at this moment and you must show to examiners
that you know a lot about Tuberous sclerosis.
Look for other features of Tuberous sclerosis such as subungual/ periungual
fibromas ( next image -a common mistake for majority of candidates is they
usually look hard at patient's hand and forget that these can be present over
patient's toes as well), Ash-leaf patches ( hypopigmeted) and Shagreen patches.
always suggest to examiners you would like to expose patient properly to
look for these skin lesions but if time is limited, at least spend some time
to look at patient's back!.
After you complete your physical examination, tell examiners that you
would be interested to look at the fundus and you are expecting to find
retinal hamatormas and check the abdomen to look for ballotable kidney
(due to renal hamartoma).
172. After these steps, you should suggest to examiners that you would get a
complete family history of similar problem and take history from patient
about epilepsy.
You would be
interested to test the
patient's IQ.One
common mistake
candidates make in
exam is they tend to
forget to look for signs
suggesting side
effects of anti-epilespy
medications.
Look hard for signs suggesting pheytoin side effects such as cerebellar
signs, gum hypertrophy and hirsutism. Also look for side effects of other
anti-epileptic!
173. Common questions examiners would ask you
1) What can you usually find in this patient's CT brain?
2) How do you manage this patient?
174. Conclusion
This gentleman has tuberous sclerosis.
Extra points
TSC is caused by defects, or mutations, on two genes-TSC1 and
TSC2. Only one of the genes needs to be affected for TSC to be
present. The TSC1 gene, discovered in 1997, is on chromosome 9 and
produces a protein called hamartin. The TSC2 gene, discovered in
1993, is on chromosome 16 and produces the protein tuberin.
175. 39-You are the SHO in charge of the medical unit
Mr Smith, an ex-IVDU was admitted to your hospital
1 week ago due to shortness of breath. CXR
revealed bi-hilar haziness and your consultant
thought that he was suffering from pneumocystis
carinii pneumonia. He responded to your treatment
and you are asked by your consultant to ask
permission from him for HIV testing.
You have 14min until the patient leaves the room, followed by 1min
for reflection before the discussion with the examiners.
176. Discussion
Pre-test counselling for HIV is always a common scenario in MRCP
PACES. Candidates always find that they have problem to tell patient's
the diagnosis (PCP) and then switch the topic of discussion form PCP
to HIV testing.
I always tell my junior doctors that before going into deep discussion
with the patient, always assess the patient's understanding about his
problem.
Therefore, after introducing yourself and a few simple questions like"
How do you feel today?" I would start off by asking" Mr Smith, I learned
that you were admitted to our hospital about one week ago, did anyone
tell you what's wrong with you?" You may be surprised to find out how
little patient knows about his condition.
Then you can briefly talk about Pneumocystis Carinii Pneumonia and
tell patient that he feels better because of the treatment. After this, a lot
of candidates find it difficult to talk about HIV and how to switch the
topic of discussion from PCP to HIV.
177. I find a solution to this problem, I would suggest to you that you may
want to try to explain to patient that it is rather rare for you to find young
adults to get PCP infection and mention that there are a few conditions
that can prone him to get this infection.
Mention HIV as one of them and proceed to assess patient's
understanding about HIV. After this, explain to patient about HIV,
relevant information to be included are what HIV is, mode of
transmission, possible long term complications and treatment. Do not
forget to get futher sexual history and social history from patient.
After this, assess patient's risk about HIV infection and ask him
whether he has any question to ask you about HIV. Explain to patient
that your consultant and you think that it is necessary for him to have
HIV testing.
Explain to him how the test is performed and how to interpret positive
and negative results. Mention about possibilities of false negative and
positive results as well.
178. Remember to explain the difference of HIV and AIDS.
Convince the patient about the benefit of early detection and
reassure him that the test result is confidential.
If you have time , you should discuss with patient about the
implication of the test result regarding to future insurance purchase.
Before you end your interview with patient, tell him that your hospital
has a special trained nurse to give him further counselling if he has
further question to discuss.
Arrange next appointment date if he is undecided about the test.
remember that if patient is not agreeable with you about something,
always ask him the reason behind this!
179. Common questions examiners would ask you
1) What is 'window period ' for HIV?
2) If the patient is married and turns out to be postive for the HIV test,
would you tell his wife if he refuses to tell his wife about the result?
181. Discussion
A popular skin station in MRCP exam. All candidates would pick up the
physical signs and come to a diagnosis after inspection
Vitiligo is a chronic skin disease that causes loss of pigment,
resulting in irregular pale patches of skin.
Vitiligo is always described as " hypopigmented patches with white
hairs in vitiliginous area".
Areas commonly involved include perioral, periorbital, axilla , upper and
lower limbs.
however, examiners would only pass you if you know how to examine
systematically a patient with vitiligo.
After your initial inspection, try to look at the patient's scalp for white
hair and alopecia ( vitiligo is associated with alopecia areata).
Then, proceed to look for jaundice ( autoimmune hepatitis), pallor
(pernicious anaemia) and thyroid swelling.
182. Remember that you must suggest to examiners that you would like to
check for postural drop of blood pressure which may suggest
Addision's disease and check urine for Diabetes Mellitus.
Look for other autoimmune diseases as well such as Rheumatoid
arthritis, SLE etc.
However, always remember that patients with leprosy or Pityriasis
versicolor may have hypopigmented skin but the hypopigmented skin
tend to be more localized.
You would find reduced sensation at the hypopigmented skin if you
suspect leprosy.
There are various available treatment for vitiligo.
Topical steroid may be useful at initial stage.Other topical
immunomodulators may be useful such as calcipotriene and
tacrolimus.
Combinations of therapy often give better results than single modalities.
These include calcipotriol with PUVA (Psoralen ultraviolet A therapy )
and tacrolimus with laser.
183.
184. Common questions examiners would ask you
1) What are the associated conditions in vitiligo?
2) How do you manage this patient?
185. Conclusion
This lady has vitiligo.
Extra points
About 20-25% of patients has other cutaneous and systemic
diseases associated with vitiligo.
188. Discussion
I show your this case again because I would like to warn you that you
may only find subtle sign in gout during you MRCP PACES exam.
My friend was asked to examine a patient's hand in his MRCP PACES
in Singapore, actually , he couldn't find any positive signs and he was
so panic until he found a small tophi over the patient's ear lobe.
Such as in this patient, you only notice a small swelling over her left
index finger. However, the diagnosis of gout would be clear if you take
a few seconds to look at her face before touching the patient.
Now, the diagnosis is clear, you are dealing with gout. The lesson to be
learned here is, when you are asked to examine a patient's hand in
MRCP PACES, look at the patient's lower limb and the face as well.
You might save a lot of time struggling to get the diagnosis if you spend
a few more seconds to inspect the patient properly. I would like to
remind you that in Station 5, you would get the diagnosis most of the
time after inspecting the patient ( except in fundoscopy, of course!).
189. Common questions examiners would ask you
1) How do you diagnose gout?
2) What may be the mechanism of a patient with gout to have renal
impairment?
( obstructive uropathy and NSAID abuse)
191. 42-Station 4: You are the SHO in charge of
ICU.
Subject: Mr Lee Xin Yan 22 years old
Mr Lee was admitted to your hospital due to motor vehicle accident 3
days ago. He sustained a severe brain injury with massive intra-cranial
haemorhage. He showed no sign of improvement. His sedation was off
24 hours ago and he showed no sign of waking up. Your consultant
has reviewed him. He and another consultant have performed a few
tests and confirmed that he is brain death. Currently, Mr Lee is being
ventilated in ICU. You are asked to talk to his mother Madam Liu about
the brain death and discuss with her the possibility of organ donation.
You have 14min until the patient leaves the room, followed by
1min for reflection before the discussion with the examiners.
192. Discussion
This type of question is always popular in MRCP PACES station 4.
There are two tasks here, the first one- you are expected to break the
bad news about brain death to Madam Liu about her son.
The second task, you are supposed to discuss about organ donation
with Madam Liu.
A lot of candidates told me that they actually have problems to explain
brain death to patient’s family members, therefore they couldn’t even
start talking about organ donation.
I think it is a common dilemma in examination, you fail to convince
patient’s mother that the patient is dead, how can you possibly proceed
to tell her about organ donation.
The principles are simple, always do the following steps in your exam
(especially in breaking bad news!)
193. a) Assess your subject understanding about a situation
In this case, you can ask Madam Liu, “I know that you son was
admitted to our hospital 3 days ago, did anyone inform you about his
condition?”
b) Assess your subject about his/her expectation about a
situation
You can ask Madam Liu,” Did you visit your son in ICU this morning,
what do you think about his condition as compared when he was
admitted?”
Madam Liu may tell you that she does not think that his son is
improving, her answer can give you some ideas how to approach in
the next step.
If she think that her son ‘s condition is improving, you may need more
time to explain some details such as CT scan reports etc to hint to
her that her son is not doing well.
194. c) Warming up
You need to explain to your subject some information before
breaking the bad news.
Always pause in between important sentences so that your subject
can give you some feedbacks.
d) Go to your task
After seeing your subject’s respond to your explanation above, you
then can break the bad news.
In this case, you may say that “Our consultants have been
reviewing him daily since he was admitted, they have reviewed his
brain scan and actually they have done a few special tests,
unfortunately, your son’s condition is not improving.”
Always remember to give your subject to breath and avoid
bombarding him/her with a lot of technical details. Try to avoid
medical jargon in exam!
195. You will be expecting that Madam Liu could not accept that her son is dead.
You certainly should empathize with your subject and NEVER rush or push
her to accept your explanation.
Here comes the dilemma, the subject could not accept her son is dead,
how do I talk about organ donation?
You actually can explore some social history about Mr Lee. Actually, my
friend failed this case in his MRCP PACES because he did not explore
about the patient’s social history and found out that Mr Lee is the only child
in the family.
After that, just tell Madam Liu that from the social history you gather from
her , her son is a very helpful young man, you explain to her that even
though Mr Lee is no more here, he is still able to help other needy people.
Madam Liu may ask you the way to do this , then you can start the topic by
saying ” Have you heard of organ donation before?”
So....., you see , the mission is accomplished! The rest of the topic such as
“What is organ donation?” etc would be a simple job for you all!
197. Discussion
I think that this type of case is still a possiblilty in your MRCP PACES,
although you are often see this case in Orthopedics ward rather than
Medical ward.
You notice this patient has right claw hand.Yes, you are right ,she has
ulnar nerve palsy!
Remember that ulnar nerve supplies all small muscles of the hand
except LOAF ( the Lateral two lumbricals, Opponens pollicis, Abductor
pollicis brevis and Flexor pollicis brevis).
As a medical student before,you might still remember the function of
lumbricals is to flex the metacarpophalageal joints and extend
interphalageal joints of fingers except thumb.
Therefore you see this this lady has claw hand involving only ring and
little fingers. (because the lateral two lumbricals are supplied by median
nerve)
198. In you exam, you must always try to find the underlying cause for this, if
you look hard , you notice that there is a scar over the patient’s wrist.
She actually sustained
industrial injury before
and there is injury of her
ulnar nerve over her
wrist.
superficial branch ( innervating the palmar aspect of the medial side of
the little finger and the adjacent sides of the little and ring fingers) and the
deep branch.( which supplies the small muscles of the hand).
As you might remember,
ulnar nerve enters the
palm anterior to the
flexor retinaculum
alongside the lateral
border of the pisiform
bone and divides into
199. If you ask the
patient to grasp
a piece of
paper between
the thumb and
lateral aspect of
the forefinger
with each hand
as below, you
would be able
to demonstrate
Froment’s
sign.
You notice that the affected thumb will flex ( Flexor pollicis brevis)
because of loss of the adductor of the thumb.
200. Common questions examiners would ask you
1) What is ulnar nerve paradox?
2) All small muscles of hand are supplied by ulnar nerve except what
muscles?
201. Conclusion
This lady has right ulnar nerve palsy due to previous trauma
Extra points
Besides the cutanous branch of superficial branch of the ulnar nerve, it
also gives branch to supply palmaris brevis ( muscular branch).
203. Discussion
This case is always very popular in MRCP station 5. A lot of candidates
can pick up the diagnosis but are unable to perform well in this case.
It is a gift if you are asked about acromegaly in MRCP PACES.
I always like to do the following if I suspect acromegaly in exam:
Spend a few seconds in general inspection
Start off by examining the patient’s hand, you notice that she has spade
–like ,sweaty hand, the skin is thickened and doughy.
Check for carpal tunnel syndrome
Look at the face- check for prognathism ( causing malocclusion of jaw),
prominent supra-orbital ridges, wide spaced interdental space, big
tongue.
Offer to look for skin tag ( molluscum fibrosum) at axilla
Look at lower limbs for pitting oedema to suggest high cardiac output
failure
204.
205. After showing all the positive signs, suggest to examiners you would
like to complete your physical examination by:
Check her Blood Pressure which is a indicator for active disease
Check urine for glycouria/ haematuria due to possible concomitant
diabetes mellitus or stone because of hypercalciuria
Check fundus to for changes of DM/hypertension and angiod streak
Compare patient with old photos
Examine CVS to look for heart failure, neck for goiter and abdomen
for hepatosplenomegaly
Check for proximal myopathy by asking patient to squat down
Check for bitemporal hemianopia-acromegaly tends to be due to
macroadenoma
206. Common questions examiners would ask you
What are the indicators for disease activity in acromegaly?
How do you manage investigate this lady?
207. Conclusion
This lady has acromegaly due to pituitary macroadenoma.
Extra points
Indicators for disease activity are uncontrolled symptoms such as
headache, sweating, presence of skin tags, uncontrolled Diabetes,
hypertension and progressive visual impairment.
After your presentation, always tell the examiners what you think about
the disease activity.
Most important test to diagnose acromegaly is non-suppressibility of
growth hormone level after an oral glucose tolerance test.
208. 45-You are the SHO in charge of Neurology Ward.
Subject: Miss Sylvia, 24-year old
Miss Sylvia was diagnosed to have epilepsy about 6 months
ago but she has failed to attend your neurology clinic follow
up. For the past one month, she has been recurrently
admitted to your hospital due to seizure and you found out
that she has not been taking her medications regularly. Due
to her work as a school teacher, you also noticed that she is
still driving to school. Currently, she is admitted in your
neurology ward and your task is to discuss the management
of her epilepsy.
You have 14 min until the patient leaves the room followed by 1min for
reflection before the discussion with the examiners.
209. Discussion
Do the following if possible:
Introduction
“ Miss Sylvia, I am Dr……., the SHO in charge of this ward. How do
you feel today?”
Assess her understanding about the illness
“ I know that you were admitted to our ward due to fit one day ago, did
anyone tell you about your problem?”
Explain the diagnosis based on patient’s understanding for the illness
You need to know about patient’s understanding about an illness before
you exaplain about the illness. Some patients might know a lot about
their own illness, therefore, you can go straight to more ‘advanced’
discussion with patients.
210. Generally, when you talk about an illness, try to cover the following:
General information about an illness. Such as “Epilepsy is due to some
abnormal brain activity that causes you to have abnormal and
uncontrolled body movement.”
Possible complications about an illness if left untreated
Possible treatment- Remember that besides medications, always talk
about non-pharmacological management. Such as in this patient,
besides anti-epileptic medications, tell patient that she must learn to
protect herself by avoiding involvement of high-risk recreational activity
such as swimming.
Always assess her social support because someone needs to know
how to take care of an epileptic patient when there is a seizure.
Other important issues pertaining to the illness- such as in this patient,
the patient might want to know whether she would pass this illness to
next generation.
211. If you encounter a female patient in your exam, always think of
the possible impact of the disease and its treatment towards
pregnancy and lactation.
Besides these issues, in this case, another issue crops up for you
to discuss with the patient is the issue of driving.
Actually, a candidate failed this station in his MRCP PACES a few
years back because he did not find out the following:
1) The patient refused to eat the medications because she was
pregnant at that time and she was worried about the side effects
of the medications to her baby.
2) The candidate did not find out what was the social support for
this lady. Actually, her husband was working outstation and there
was no way for her to go to work except driving her own car.
3) The patient was very worried about passing the disease
(epilepsy) to her baby and actually wanted to ask the candidate
about abortion. However, my friend just ignored her because this
task was not mentioned in the paper.
213. Discussion:
OK, this is a common case in MRCP PACES station 5 if you are sitting
the exam in Malaysia and Singapore. I think it is easy for you to detect
the abnormality in this gentleman because the clinical signs are obvious.
You notice this gentleman has severe spine abnormalities. Yes, you are
right, he has ‘Question mark’ posture. This is due to fixed kyphoscoliosis
of the thoracic spine with compensatory extension of the cervical spine.
This case is easy but you must remember to look for these spine
abnormalities especially if you are seeing a patient who is lying in bed
during your MRCP PACES exam because the kyphoscoliosis may not be
obvious and can be masked by a pillow behind the patient’s back.
Patients with Ankylosing Spondylitis usually present with back pain
and this gentleman has chronic back pain since the age of 20 years old.
214. Proceed to do the following after a general inspection:
ask the patient to walk away from you and turn back and walk towards you.
Pay attention to patient’s posture.
ask patient to look to either side. You will notice patient may have limited
cervical spine movement. The patient may need to move his whole body
when he wants to look to either side.
check his thoracic and lumbar spine movement , usually, I would ask patient to flex
aside(lateral flexion), rotate and do forward and backward flexion. Remember to fix
the patient pelvis when you ask patient to do rotation. You will notice patient with
Ankylosing Spondylitis has very limited spine movement.
you need to do two tests to demonstrate the patient has limited spine
movement by demonstrating ‘occiput to wall’ test and Schober’s test. In
following picture, when I ask the patient to rest his back against the wall,
you notice that this gentleman has difficulty to make contact his head
against the wall.
for Schober’s test, mark two points, one 10 cm above and one 5 cm
below a line joining the ‘dimple of Venus’ on the sacral promontory. An
increase in the separation of less than 5 cm when the patient does a
forward flexion signifies limited spine movement.
215. after these tests, check peripheral joints especially hands and also look
for possibility of psoriasis ( because one variant of psoriatic arthropathy
may look like Ankylosing spondylitis)
suggest to examiners you will like to look for 4As- Anterior uveitis, Apical
fibrosis, Aortic regurgitation and Achilles tendinitis.
216. Common questions examiners would ask you
What are the diagnostic criteria to diagnose Ankylosing Spondylitis?
How do you manage this gentleman?( Remember that genetic
counseling is important and remember to talk about HLA-B27!)
217. Conclusion:
This gentleman has Ankylosing Spondylitis with limited spine
movement.
Extra points:
Diagnostic criteria of Ankylosing Spondylitis is based on New York
Criteria (1966)
Limitation of motion of the lumbar spine in all 3 planes: anterior flexion,
lateral flexion and extension.
History of the presence of pain at the dorsolumbar junction or in the
lumbar spine.
Limitation of chest expansion to 1 inch (2.5 cm) or less, measured at the
level of the fourth intercostal space
218. I find the following algorithm interesting and helpful
