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Dhaka Medical College Hospital
Weekly Grand Round
Presentation
A CASE OF A 14 YEAR
OLD BOY WITH LIMB
WEAKNESS MEDICINE UNIT VIII
Department of Medicine
ABOUT THE
PATIENT 01
PARTICULARS OF THE PATIENT
AGE
GENDER
LOCATION
14
Male
Nakla, Sherpur
MD
MUNNA OCCUPATION
Madrasa Student
PRESENTING
COMPLAINTS 02
PRESENTING COMPLAINTS
Unable to swallow and
speak for 5 days
Confusion and
excessive sleepiness
for 15 days
Weakness of all
four limbs for 20
days
01
02
03
THE HISTORY 03
HISTORY OF PRESENT
ILLNESS
● According to the statement of his sister, he was reasonably well one
month back.
● His illness started with weakness in the right lower limb, initially
associated with pain.
● The pain subsided and the weakness progressively involved the right side
of the trunk, right upper limb, the left lower limb and then to left upper
limb over a period of 3 weeks. He did not complain any numbness.
HISTORY OF PRESENT
ILLNESS
● During this period, he was remarkably sleepy, tired, had difficulty in walking
due to loss of balance. He frequently complained of headache.
● With these complaints he repeatedly consulted Paediatric Neurology
Department in BSMMU on OPD basis first and then got admitted.
● Medical records show that he had ataxia, nystagmus, hypertonia, hyper-
reflexia and extensor plantar reflex with urinary incontinence at the time of
admission on September, 2022.
● During the 12 days of admission his condition deteriorated progressively. He
developed dysphagia, dysarthria, dysphonia and GCS level went down from 15
to 9. So, he was referred to DMCH.
● While in DMCH his conditions initially worsened, GCS dipped down to 3. Then
his condition started to improve and GCS was 13 by day 5 of admission. His
urinary incontinence and dysphagia resolved. Significant muscle weakness
persisted.
HISTORY OF PRESENT ILLNESS
● Now the patient can walk albeit with support, GCS persists at 15.
● He had no fever or seizure at any point. There is no history of any preceding
illness or contact with TB patient. His bowel habit was normal throughout.
HISTORY OF PRESENT ILLNESS
OTHER RELEVANT HISTORY
HISTORY OF PAST ILLNESS
Nothing of significance
PERSONAL HISTORY
Active teenage student. Plays
football. Non-smoker, no history of
narcotic use
SOCIOECONOMIC HISTORY
Comes from a lower middle class
family
FAMILY HISTORY
Patient has an elder sister. Both
parents alive and well (No
consanguinity). No history of similar
illness in either side of the family.
TRAVEL HISTORY
No travel history outside of Dhaka and
Sherpur in last one year
IMMUNISATION HISTORY
PHYSICAL
EXAMINATION 04
An ill-looking young man
who is very drowsy and
confused
04
PHYSICAL EXAMINATION: GENERAL
PERFORMED ON 29 SEP
Appearance Semi-conscious, ill-looking, vacant expression
Anemia/Jaundice/Cyanosis Absent
Clubbing Absent
Koilonychia/ Leukonychia Absent
Edema Absent
Lymphadenopathy Absent
BP 100/70mmHg
Pulse 72/min
Temperature Normal
Respiration Normal, SpO2 100% on air
SYSTEMIC EXAMINATION
Detailed neurological
examination was
difficult due to the
patient’s fluctuating
level of consciousness.
The most detailed neuro
exam could be carried
out on 03 OCT
Other systemic
examination yielded no
positive findings
Patient kept drifting off while examination
CRANIAL NERVES
Could not be performed due to low level of consciousness
MOTOR
RU RL LU LL
Tone
Strength Could not be assessed due to low
level of consciousness
DEEP TENDON REFLEXES
Biceps Triceps Supinator Knee Ankle
R
All are exaggerated without clonus
L
SYSTEMIC EXAMINATION: NERVOUS SYSTEM
PERFORMED ON 29 SEP
GCS
7/15 (E4V2M1)
PLANTAR REFLEX
Flexor Bilaterally
CRANIAL NERVES
II, III, IV, VI Significant palsy in right lateral
gaze, right eye; upward gaze,
both eyes
Nystagmus on both lateral gazes.
Saccadic eye movement with
broken pursuit
V Sensations Intact,
Significant weakness,
symmetrical
VII Symmetrical weakness
IX, X Could not cough or open
mouth wide enough
XI, XII Symmetrical Weakness
MOTOR
RU RL LU LL
Tone
Strength 1/5 2/5 1/5 2/5
DEEP TENDON REFLEXES
Biceps Triceps Supinator Knee Ankle
R
All are exaggerated without clonus
L
SYSTEMIC EXAMINATION: NERVOUS SYSTEM
PERFORMED ON 3 OCT
GCS 14/15 (E4V4M6)
PLANTAR REFLEX
Flexor Bilaterally
COORDINATION
Could not perform due to weakness
GAIT
Could not perform due to weakness
SENSORY SYSTEM
All sensory modalities intact throughout the
body
SYSTEMIC EXAMINATION: NERVOUS SYSTEM
PERFORMED ON 3 OCT
HIGHER PSYCHIC FUNCTION
MMSE Score 20/30
OPHTHALMOSCOPY
Normal findings
TIMELINE OF
PROGRESSION 05
TIMELINE OF DISEASE PROGRESSION
First symptom appears: Right lower leg pain
27 AUG
Developed headaches and sleepiness
30 AUG
BSMMU Outpatient consultation
2 SEP
Leg pain and headache settles. Sleepiness remains. Notices
weakness in right leg
4 SEP
Develops urinary incontinence. Weakness worsens
15 SEP
Repeat BSMMU outpatient consultation. Exaggerated DTR, Babinsky
sign, Nystagmus, Ataxia found on exam. Admission.
17 SEP
Dysphagia appears. GCS dips to 9. ICU advice anticipating
respiratory muscle paralysis
25 SEP
Admitted to DMCH. GCS 7. Plantar returns to flexor.
29 SEP
Condition worsens. GCS goes down to 3. No respiratory paralysis.
30 SEP
Level of consciousness improves but fluctuating. GCS 7 (E4V2M1)
01 OCT
TIMELINE OF DISEASE PROGRESSION
Condition keeps improving. Muscle power MRC 1 /2 across limbs.
GCS 12/15. Keeps drifting off.
02 OCT
NG removed, can swallow liquids. Incontinence resolves. Party
decides to leave
03 OCT
Consciousness level worsened, not arousable for most of the day.
Contacts DMCH and advised to admit. Improves spontaneously late
in the evening, stays home.
06 OCT
Can walk with support. Drowsiness decreased but still significant.
09 OCT
Comes in for follow up?
12 OCT
TIMELINE OF DISEASE PROGRESSION
SALIENT FEATURES
A 14 year old fit madrasa student
develops leg pain and weakness
Pain subsides but the weakness
ascends and affects all limbs
At the same time he develops
headache and excessive
sleepiness
He eventually developed
ophthalmoplegia, ataxia, dysphagia,
Dysarthria
At no point was there any fever.
There was no history of
preceding illness
Over the course of a month his
weakness and drowsiness
worsened
Examination revealed
hypertonicity and hyperreflexia.
Plantar initially extensor, then
flexor
Sensory modalities were intact
throughout
Provisional Diagnosis
Autoimmune Encephalitis
DIFFERENTIAL DIAGNOSIS
BICKERSTAFF
BRAINSTEM
ENCEPHALITIS
A
NEUROMYELITIS
OPTICA
C
B
D
GUILLEN
BARRE
SYNDROME
TB
ENCEPHALITIS
INVESTIGATIONS 07
INVESTIGATIONS
HEMATOLOGY (28 Aug 2022)
Haemoglobin 13.6 g/dl
ESR 05 mm in 1st hour
Total Count 8200/ cm3
Differential Count Neutrophil: 55%
Lymphocytes: 34%
Monocytes: 07%
Eosinophil: 04%
Circulating Eosinophils 328/cm3
Platelet Count 2,82,000/cm3
RBC Count 5.02 m/microlitre
Hematocrit 42.3%
HEMATOLOGY (20 Sep 2022)
Haemoglobin 13.3 g/dl
ESR 04 mm in 1st hour
Total Count 11000/ cm3
Differential Count Neutrophil: 92%
Lymphocytes: 06%
Monocytes: 02%
Eosinophil: 00%
Circulating Eosinophils 328/cm3
Platelet Count 3,82,000/cm3
RBC Count 4.07 m/ml
Hematocrit 41.2%
INVESTIGATIONS
BIOCHEMISTRY
CRP 0.22 mg/L
Creatinine 0.83 mg/dL
AST 10 U/L
S Electrolytes Na+ 138.00 mmol/L
K+ 4.62 mmol/L
Cl- 102.00 mmol/L
SEROLOGY
ASO Titre 200 IU/mL
AntiDsDNA 11.0 U/mL
ANA Negative
SARS-COV2 Negative
HBsAg Negative
INVESTIGATIONS
CSF STUDY
Volume 1 ml
Color Watery
Appearance Clear
WBC Count 03 Cells/ cm3
Neutrophils 20%
Lymphocyte 80%
CSF STUDY
Glucose 6.1 mmol/L
Protein 1.0 gm/L
Chloride 115mmol/L
Gram Stain No organism seen
AFB No organism seen
ADA 15.0 u/L
GeneXpart Negative
INVESTIGATIONS
IMAGING
MRI BRAIN No abnormalities seen
MRI Spine No abnormalities seen
AUTOIMMUNE ENCEPHALITIS PANEL
NMDA Negative
AMPA Negative
GABA-B Negative
LGi-1 Negative
Anti GQ1b Ab Pending
NEUROPHYSIOLOGICAL STUDIES
EEG Normal
NCS and EMG No peripheral demyelination
or axonal damage. During
voluntary activation there
is no interference or
activation suggestive of
central cause of motor
weakness
The Diagnosis
Bickerstaff’s Brainstem
Encephalitis

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A case of a 14 year old boy with limb weakness.pptx

  • 1. Dhaka Medical College Hospital Weekly Grand Round Presentation A CASE OF A 14 YEAR OLD BOY WITH LIMB WEAKNESS MEDICINE UNIT VIII Department of Medicine
  • 3. PARTICULARS OF THE PATIENT AGE GENDER LOCATION 14 Male Nakla, Sherpur MD MUNNA OCCUPATION Madrasa Student
  • 5. PRESENTING COMPLAINTS Unable to swallow and speak for 5 days Confusion and excessive sleepiness for 15 days Weakness of all four limbs for 20 days 01 02 03
  • 7. HISTORY OF PRESENT ILLNESS ● According to the statement of his sister, he was reasonably well one month back. ● His illness started with weakness in the right lower limb, initially associated with pain. ● The pain subsided and the weakness progressively involved the right side of the trunk, right upper limb, the left lower limb and then to left upper limb over a period of 3 weeks. He did not complain any numbness.
  • 8. HISTORY OF PRESENT ILLNESS ● During this period, he was remarkably sleepy, tired, had difficulty in walking due to loss of balance. He frequently complained of headache. ● With these complaints he repeatedly consulted Paediatric Neurology Department in BSMMU on OPD basis first and then got admitted. ● Medical records show that he had ataxia, nystagmus, hypertonia, hyper- reflexia and extensor plantar reflex with urinary incontinence at the time of admission on September, 2022.
  • 9. ● During the 12 days of admission his condition deteriorated progressively. He developed dysphagia, dysarthria, dysphonia and GCS level went down from 15 to 9. So, he was referred to DMCH. ● While in DMCH his conditions initially worsened, GCS dipped down to 3. Then his condition started to improve and GCS was 13 by day 5 of admission. His urinary incontinence and dysphagia resolved. Significant muscle weakness persisted. HISTORY OF PRESENT ILLNESS
  • 10. ● Now the patient can walk albeit with support, GCS persists at 15. ● He had no fever or seizure at any point. There is no history of any preceding illness or contact with TB patient. His bowel habit was normal throughout. HISTORY OF PRESENT ILLNESS
  • 11. OTHER RELEVANT HISTORY HISTORY OF PAST ILLNESS Nothing of significance PERSONAL HISTORY Active teenage student. Plays football. Non-smoker, no history of narcotic use SOCIOECONOMIC HISTORY Comes from a lower middle class family FAMILY HISTORY Patient has an elder sister. Both parents alive and well (No consanguinity). No history of similar illness in either side of the family. TRAVEL HISTORY No travel history outside of Dhaka and Sherpur in last one year IMMUNISATION HISTORY
  • 13. An ill-looking young man who is very drowsy and confused 04
  • 14. PHYSICAL EXAMINATION: GENERAL PERFORMED ON 29 SEP Appearance Semi-conscious, ill-looking, vacant expression Anemia/Jaundice/Cyanosis Absent Clubbing Absent Koilonychia/ Leukonychia Absent Edema Absent Lymphadenopathy Absent BP 100/70mmHg Pulse 72/min Temperature Normal Respiration Normal, SpO2 100% on air
  • 15. SYSTEMIC EXAMINATION Detailed neurological examination was difficult due to the patient’s fluctuating level of consciousness. The most detailed neuro exam could be carried out on 03 OCT Other systemic examination yielded no positive findings
  • 16. Patient kept drifting off while examination
  • 17. CRANIAL NERVES Could not be performed due to low level of consciousness MOTOR RU RL LU LL Tone Strength Could not be assessed due to low level of consciousness DEEP TENDON REFLEXES Biceps Triceps Supinator Knee Ankle R All are exaggerated without clonus L SYSTEMIC EXAMINATION: NERVOUS SYSTEM PERFORMED ON 29 SEP GCS 7/15 (E4V2M1) PLANTAR REFLEX Flexor Bilaterally
  • 18. CRANIAL NERVES II, III, IV, VI Significant palsy in right lateral gaze, right eye; upward gaze, both eyes Nystagmus on both lateral gazes. Saccadic eye movement with broken pursuit V Sensations Intact, Significant weakness, symmetrical VII Symmetrical weakness IX, X Could not cough or open mouth wide enough XI, XII Symmetrical Weakness MOTOR RU RL LU LL Tone Strength 1/5 2/5 1/5 2/5 DEEP TENDON REFLEXES Biceps Triceps Supinator Knee Ankle R All are exaggerated without clonus L SYSTEMIC EXAMINATION: NERVOUS SYSTEM PERFORMED ON 3 OCT GCS 14/15 (E4V4M6)
  • 19. PLANTAR REFLEX Flexor Bilaterally COORDINATION Could not perform due to weakness GAIT Could not perform due to weakness SENSORY SYSTEM All sensory modalities intact throughout the body SYSTEMIC EXAMINATION: NERVOUS SYSTEM PERFORMED ON 3 OCT HIGHER PSYCHIC FUNCTION MMSE Score 20/30 OPHTHALMOSCOPY Normal findings
  • 21. TIMELINE OF DISEASE PROGRESSION First symptom appears: Right lower leg pain 27 AUG Developed headaches and sleepiness 30 AUG BSMMU Outpatient consultation 2 SEP Leg pain and headache settles. Sleepiness remains. Notices weakness in right leg 4 SEP Develops urinary incontinence. Weakness worsens 15 SEP
  • 22. Repeat BSMMU outpatient consultation. Exaggerated DTR, Babinsky sign, Nystagmus, Ataxia found on exam. Admission. 17 SEP Dysphagia appears. GCS dips to 9. ICU advice anticipating respiratory muscle paralysis 25 SEP Admitted to DMCH. GCS 7. Plantar returns to flexor. 29 SEP Condition worsens. GCS goes down to 3. No respiratory paralysis. 30 SEP Level of consciousness improves but fluctuating. GCS 7 (E4V2M1) 01 OCT TIMELINE OF DISEASE PROGRESSION
  • 23. Condition keeps improving. Muscle power MRC 1 /2 across limbs. GCS 12/15. Keeps drifting off. 02 OCT NG removed, can swallow liquids. Incontinence resolves. Party decides to leave 03 OCT Consciousness level worsened, not arousable for most of the day. Contacts DMCH and advised to admit. Improves spontaneously late in the evening, stays home. 06 OCT Can walk with support. Drowsiness decreased but still significant. 09 OCT Comes in for follow up? 12 OCT TIMELINE OF DISEASE PROGRESSION
  • 24. SALIENT FEATURES A 14 year old fit madrasa student develops leg pain and weakness Pain subsides but the weakness ascends and affects all limbs At the same time he develops headache and excessive sleepiness He eventually developed ophthalmoplegia, ataxia, dysphagia, Dysarthria At no point was there any fever. There was no history of preceding illness Over the course of a month his weakness and drowsiness worsened Examination revealed hypertonicity and hyperreflexia. Plantar initially extensor, then flexor Sensory modalities were intact throughout
  • 28. INVESTIGATIONS HEMATOLOGY (28 Aug 2022) Haemoglobin 13.6 g/dl ESR 05 mm in 1st hour Total Count 8200/ cm3 Differential Count Neutrophil: 55% Lymphocytes: 34% Monocytes: 07% Eosinophil: 04% Circulating Eosinophils 328/cm3 Platelet Count 2,82,000/cm3 RBC Count 5.02 m/microlitre Hematocrit 42.3% HEMATOLOGY (20 Sep 2022) Haemoglobin 13.3 g/dl ESR 04 mm in 1st hour Total Count 11000/ cm3 Differential Count Neutrophil: 92% Lymphocytes: 06% Monocytes: 02% Eosinophil: 00% Circulating Eosinophils 328/cm3 Platelet Count 3,82,000/cm3 RBC Count 4.07 m/ml Hematocrit 41.2%
  • 29. INVESTIGATIONS BIOCHEMISTRY CRP 0.22 mg/L Creatinine 0.83 mg/dL AST 10 U/L S Electrolytes Na+ 138.00 mmol/L K+ 4.62 mmol/L Cl- 102.00 mmol/L SEROLOGY ASO Titre 200 IU/mL AntiDsDNA 11.0 U/mL ANA Negative SARS-COV2 Negative HBsAg Negative
  • 30. INVESTIGATIONS CSF STUDY Volume 1 ml Color Watery Appearance Clear WBC Count 03 Cells/ cm3 Neutrophils 20% Lymphocyte 80% CSF STUDY Glucose 6.1 mmol/L Protein 1.0 gm/L Chloride 115mmol/L Gram Stain No organism seen AFB No organism seen ADA 15.0 u/L GeneXpart Negative
  • 31. INVESTIGATIONS IMAGING MRI BRAIN No abnormalities seen MRI Spine No abnormalities seen AUTOIMMUNE ENCEPHALITIS PANEL NMDA Negative AMPA Negative GABA-B Negative LGi-1 Negative Anti GQ1b Ab Pending NEUROPHYSIOLOGICAL STUDIES EEG Normal NCS and EMG No peripheral demyelination or axonal damage. During voluntary activation there is no interference or activation suggestive of central cause of motor weakness