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INTERESTING CASE OF ANAEMIA
S.DHANRAJ PG M2
DR.SUNDARAMURTHY’S UNIT
• 40 YRS OLD MRS.SARASU CAME WITH
C/O on 4/4/13
Decreased urine output – 15 days
-- gradual
-- 300ml/day
Abdominal pain -- 6 months
-- pricking,more towards
epigastric region,not radiating or referred,not assoc. with
any other symptoms
Fever -- on and off,10 days
-- low grade
intermittent, not assoc. with
chills,rigor,rash,bleeding tendency
• Leg swelling -- 15 days
-- bilateral,upto knee
No h/o abdominal distention
No h/o constipation
No h/o chest pain/ breathlesness
No h/o jaundice
h/o hair fall +
h/o easy fatigueability+
h/o loss of apetite
No h/o contact
No h/o trauma
No h/o loc, no h/o drug intake
• PAST HISTORY
Not a known DM/SHT/CAD
No previous admissions
• MENSTRUAL HISTORY
amenorrhea for 18 yrs
EXAMINATION
Drowsy
Temperature (98.4 F )
dehydrated,
Severe pallor,facial puffiness
Dry coarse skin,sparse hair in scalp
Hoarse voice
b/l pedal edema+
no clubbing,no palpable lymphadenopathy
CVS – s1s2+
RS -- B/L normal breath sounds
P/A– epigastric tenderness+
-- no organomegaly
CNS – drowsy ,responding to oral commands
-- Examination: able to move all four limbs
-- delayed DTR
VITALS : BP-90/60mmHg;
PR- 60/min
• She was initially suspected as a case of
? Chronic kidney disease with encephalopathy
and fever under evaluation
• INVESTIGATIONS
• CBC – HB 7.6 SR. ELECTROLYTES
TC 4500 Na-129
DC N70L27E3 K-3.7
ESR 15/35 CL-98
PCV 24 HCO3-23
MCV 83 URINE
MCH 26 ALB-NIL
MCHC 31 SUG-NIL
RBC 2.8LAC DEP-1-3PUS CELLS
PLATLETS 1L
• RFT- SUGAR 203
UREA 12
CREATININE 0.8
• USG– N STUDY
• CXR- PA – N STUDY
• ECG -- WNL
• ECHO -- N LV FUNCTION
• FEVER PROFILE AND BLOOD CULTURE--
NEGATIVE
• CLINICALLY , suspected
MYXEDEMA PRECOMA
TFT SENT and
 started on ELTROXIN 100mcg
WITH steroids
TFT results– FT3 - 0.37pg/ml(2.3 to 4.2pg)
FT4 – 0.41ng/dl(0.6 to 2ng)
TSH – 2.572miu/ml(1 to 5miu/ml)
ELTROXIN dose stepped up
INVESTIGATIONS
• 5/4/2013
Urine spot PCR– 23/13
p.smear– microcytic hypochromic anaemia
Wbc—N
Platelets– adequate
No immature cells/haemoparasite
• Reticulocyte count – 1.5% (0.5-1.5%)
•
• Se LDH 190 U/L (135-220)
• Coomb’s test: negative
• Serum iron: 48 (50 to 150mcg/dl)
• TIBC: 380 (300-360 mcg/dl)
• Serum ferritin : 28 (30 to100mcg/dl)
• 7/4/13
patient started showing improvement
FURTHER INVESTIGATIONS
With TFT results (low t3, t4, normal TSH)
a pituitary cause of hypothyroid was
suspected and
PROCEEDED FOR workup for endocrine
insufficiency
• PROLACTIN – 0.6ng/ml (4.7 to 23.3 ng)
• LH – 0.99miu/ml
( Follicular phase:2.4-12.6
Ovulation phase:14-95.6
Luteal phase: 1-11.4 mIU/ml)
• FSH – 3.14 miu/ml
( Follicular phase: 3.5-12.5
Ovulation phase: 4.7-21.5
Luteal phase: 1.7-7.7 mIU/ml)
• CORTISOL – 0.42mcg/dl ( 6.2 – 19.4 mcg/dl)
• ACTH – 3.07pg/ml (7.2 – 63.3 pg/ml)
• Patient was continued with Levothyroxine
and steroids
• Patient improved dramatically
ON PROBING
She gave
• h/o post partum haemorrhage at 3rd delivery
• Lactation failure after 3rd delivery
• Amenorrhea for 18 years
• PROCEEDED WITH MRI BRAIN
FINAL DIAGNOSIS
• EMPTY SELLA SYNDROME probably due to
POSTPARTUM PITUITARY NECROSIS
(SHEEHAN’S SYNDROME)
INVESTIGATIONS NOT DONE
• Stimulation and provocative tests
• Posterior pituitary hormones assay
• Autoimmune work up----primary hypophysitis
(lymphocytic, granulomatous)
• Secondary hypophysitis—(infections,
sarcoidosis, takayasu)
• Haematological malignancy
SHEEHAN’S SYNDROME
- Postpartum hypopituitarism caused by
necrosis of the pituitary gland
- It is usually the result of severe
hypotension or shock caused by
massive hemorrhage during or
after delivery
- Usually presents as anterior pituitary
hormone deficiency
- Evolves slowly and is diagnosed late
- most common cause of hypopituitarism in
developing countries
- prevalence to be about 3% for women
above 20 years of age
- average time between the previous
obstetric event and diagnosis of SS was 6
to 13 years
MECHANISM
• Ischemic pituitary necrosis due to
severe postpartum hemorrhage
• Vasospasm, thrombosis and
vascular compression of the
hypophyseal arteries
• Autoimmunity
PRESENTATION
SYMPTOMS
• CORTICOTROPIN DEFICIENCY can cause
weakness, fatigue, hypoglycemia, or dizziness.
• GONADOTROPIN DEFICIENCY will often cause
amenorrhea, oligomenorrhea, hot flashes, or
decreased libido.
• GROWTH HORMONE DEFICIENCY causes many
vague symptoms including fatigue, decreased quality of
life, and decreased muscle mass.
• Difficulty breast-feeding or an inability to breast-feed
• HYPOTHYROIDISM
• Some women live for years with pituitary
insufficiency, can present as ADRENAL CRISIS triggered
by extreme physical stressors, such as severe infection
or surgery.
TREATMENT
Hormone replacement
• Hydrocortisone or prednisolone is replaced first
because thyroxine therapy can exacerbate
glucocorticoid deficiency and theoretically induce
an adrenal crisis.
• thyroxine replacement
• gonadotropin replacement
• Replacement of growth hormone is necessary in
children with hypopituitarism but is controversial
in adults.
REPLACEMENT
• ACTH -- Hydrocortisone
Cortisone acetate
Prednisone
• TSH – L-Thyroxine
• FSH/LH -- Females
Conjugated estrogen (0.65–1.25 mg qd for 25 days)
Progesterone (5–10 mg qd) on days 16–25
For fertility: Menopausal gonadotropins, human CG
Males
Testosterone enanthate
• GH -- Adults: Somatotropin (0.1–1.25 mg SC qd)
Children: Somatotropin [0.02–0.05 (mg/kg per day)]
• VASOPRESSIN
THANK YOU

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A Case of Sheehan's Syndrome

  • 1. INTERESTING CASE OF ANAEMIA S.DHANRAJ PG M2 DR.SUNDARAMURTHY’S UNIT
  • 2. • 40 YRS OLD MRS.SARASU CAME WITH C/O on 4/4/13 Decreased urine output – 15 days -- gradual -- 300ml/day Abdominal pain -- 6 months -- pricking,more towards epigastric region,not radiating or referred,not assoc. with any other symptoms Fever -- on and off,10 days -- low grade intermittent, not assoc. with chills,rigor,rash,bleeding tendency
  • 3. • Leg swelling -- 15 days -- bilateral,upto knee No h/o abdominal distention No h/o constipation No h/o chest pain/ breathlesness No h/o jaundice h/o hair fall + h/o easy fatigueability+ h/o loss of apetite No h/o contact No h/o trauma No h/o loc, no h/o drug intake
  • 4. • PAST HISTORY Not a known DM/SHT/CAD No previous admissions • MENSTRUAL HISTORY amenorrhea for 18 yrs
  • 5. EXAMINATION Drowsy Temperature (98.4 F ) dehydrated, Severe pallor,facial puffiness Dry coarse skin,sparse hair in scalp Hoarse voice b/l pedal edema+ no clubbing,no palpable lymphadenopathy
  • 6. CVS – s1s2+ RS -- B/L normal breath sounds P/A– epigastric tenderness+ -- no organomegaly CNS – drowsy ,responding to oral commands -- Examination: able to move all four limbs -- delayed DTR VITALS : BP-90/60mmHg; PR- 60/min
  • 7. • She was initially suspected as a case of ? Chronic kidney disease with encephalopathy and fever under evaluation
  • 8. • INVESTIGATIONS • CBC – HB 7.6 SR. ELECTROLYTES TC 4500 Na-129 DC N70L27E3 K-3.7 ESR 15/35 CL-98 PCV 24 HCO3-23 MCV 83 URINE MCH 26 ALB-NIL MCHC 31 SUG-NIL RBC 2.8LAC DEP-1-3PUS CELLS PLATLETS 1L • RFT- SUGAR 203 UREA 12 CREATININE 0.8
  • 9. • USG– N STUDY • CXR- PA – N STUDY • ECG -- WNL • ECHO -- N LV FUNCTION • FEVER PROFILE AND BLOOD CULTURE-- NEGATIVE
  • 10. • CLINICALLY , suspected MYXEDEMA PRECOMA TFT SENT and  started on ELTROXIN 100mcg WITH steroids
  • 11. TFT results– FT3 - 0.37pg/ml(2.3 to 4.2pg) FT4 – 0.41ng/dl(0.6 to 2ng) TSH – 2.572miu/ml(1 to 5miu/ml) ELTROXIN dose stepped up
  • 12. INVESTIGATIONS • 5/4/2013 Urine spot PCR– 23/13 p.smear– microcytic hypochromic anaemia Wbc—N Platelets– adequate No immature cells/haemoparasite
  • 13. • Reticulocyte count – 1.5% (0.5-1.5%) • • Se LDH 190 U/L (135-220) • Coomb’s test: negative • Serum iron: 48 (50 to 150mcg/dl) • TIBC: 380 (300-360 mcg/dl) • Serum ferritin : 28 (30 to100mcg/dl)
  • 14. • 7/4/13 patient started showing improvement FURTHER INVESTIGATIONS With TFT results (low t3, t4, normal TSH) a pituitary cause of hypothyroid was suspected and PROCEEDED FOR workup for endocrine insufficiency
  • 15. • PROLACTIN – 0.6ng/ml (4.7 to 23.3 ng) • LH – 0.99miu/ml ( Follicular phase:2.4-12.6 Ovulation phase:14-95.6 Luteal phase: 1-11.4 mIU/ml) • FSH – 3.14 miu/ml ( Follicular phase: 3.5-12.5 Ovulation phase: 4.7-21.5 Luteal phase: 1.7-7.7 mIU/ml) • CORTISOL – 0.42mcg/dl ( 6.2 – 19.4 mcg/dl) • ACTH – 3.07pg/ml (7.2 – 63.3 pg/ml)
  • 16. • Patient was continued with Levothyroxine and steroids • Patient improved dramatically
  • 17. ON PROBING She gave • h/o post partum haemorrhage at 3rd delivery • Lactation failure after 3rd delivery • Amenorrhea for 18 years • PROCEEDED WITH MRI BRAIN
  • 18.
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  • 21. FINAL DIAGNOSIS • EMPTY SELLA SYNDROME probably due to POSTPARTUM PITUITARY NECROSIS (SHEEHAN’S SYNDROME)
  • 22. INVESTIGATIONS NOT DONE • Stimulation and provocative tests • Posterior pituitary hormones assay • Autoimmune work up----primary hypophysitis (lymphocytic, granulomatous) • Secondary hypophysitis—(infections, sarcoidosis, takayasu) • Haematological malignancy
  • 23. SHEEHAN’S SYNDROME - Postpartum hypopituitarism caused by necrosis of the pituitary gland - It is usually the result of severe hypotension or shock caused by massive hemorrhage during or after delivery - Usually presents as anterior pituitary hormone deficiency - Evolves slowly and is diagnosed late
  • 24. - most common cause of hypopituitarism in developing countries - prevalence to be about 3% for women above 20 years of age - average time between the previous obstetric event and diagnosis of SS was 6 to 13 years
  • 25. MECHANISM • Ischemic pituitary necrosis due to severe postpartum hemorrhage • Vasospasm, thrombosis and vascular compression of the hypophyseal arteries • Autoimmunity
  • 27.
  • 28.
  • 29. SYMPTOMS • CORTICOTROPIN DEFICIENCY can cause weakness, fatigue, hypoglycemia, or dizziness. • GONADOTROPIN DEFICIENCY will often cause amenorrhea, oligomenorrhea, hot flashes, or decreased libido. • GROWTH HORMONE DEFICIENCY causes many vague symptoms including fatigue, decreased quality of life, and decreased muscle mass. • Difficulty breast-feeding or an inability to breast-feed • HYPOTHYROIDISM • Some women live for years with pituitary insufficiency, can present as ADRENAL CRISIS triggered by extreme physical stressors, such as severe infection or surgery.
  • 30. TREATMENT Hormone replacement • Hydrocortisone or prednisolone is replaced first because thyroxine therapy can exacerbate glucocorticoid deficiency and theoretically induce an adrenal crisis. • thyroxine replacement • gonadotropin replacement • Replacement of growth hormone is necessary in children with hypopituitarism but is controversial in adults.
  • 31. REPLACEMENT • ACTH -- Hydrocortisone Cortisone acetate Prednisone • TSH – L-Thyroxine • FSH/LH -- Females Conjugated estrogen (0.65–1.25 mg qd for 25 days) Progesterone (5–10 mg qd) on days 16–25 For fertility: Menopausal gonadotropins, human CG Males Testosterone enanthate • GH -- Adults: Somatotropin (0.1–1.25 mg SC qd) Children: Somatotropin [0.02–0.05 (mg/kg per day)] • VASOPRESSIN