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Case presentation
Done by: Dr. Rahma ShahBahai
Medical intern
History…
 36 y.o single Saudi female k/c of HTN, T2DM and dyslipidemia
 Direct admission from OPD.
 Presented with lower back pain, headache and inability to walk
for 3 months.
 referred from KFH (Hafof) for persistent hypokalemia for further
investigation.
HPI:
 3 months Hx of progressive bilateral lower limbs weakness.
 Start as a simple weakness>>can’t carry her weight during
standing>>become wheelchair bound.
 Headache and lower back pain.
 No Hx of sphincter incontinence.
Drug Hx:
 Aldactone 50 mg PO BID
 Nifedipine 40 mg PO OD
 Hydralazine 50 mg PO Q6H
 Atorvastatin 20 mg PO OD
 Labetalol 100 mg PO BID
 Diamicron 90 mg PO OD
PH:
 uncontrolled HTN >10 years
 Dyslipidemia+T2DM ~3month
 2ry Amenorrhea ~15 yrs.
His menarche @ 13>> stopped
didn't seek medical advice.
 No surgical Hx.
FH:
 father in good health.
 Mother >>HTN
 Sis1: HTN+DM
 Sis 2: passed away (leukemia)
 sis 3: weight gain+2ry amenorrhea
Systemic review:
 No mood changes
 No dizziness
 No blurred vision
 excessive hair growth
 acne
 No respiratory or cardiac symptoms
 No nausea, vomiting, diarrhea or constipation
 No urinary symptoms
D.Dx ???
Examination…
 General:
 Obese, round face, comfortable in the bed, not in distress.
 Vitals: T 37.7 ,p 90, RR 18, BP 160/100
 Skin:
 hirsutism, facial plethora, acne, dorsocervical fat deposition, supraclavicular fat
deposition.
 Chest: clear, good air entry bilateral.
 CVS: S1,S2+0
 Abdomen: distended, White striae ~0.5-0.7 cm, positive bowel sound.
 CNS: conscious, alert
 Extremities: bruises
 U.L: power 4/5, reflexes normal
 L.L: muscles wasting, bruises, no edema, power 3/5, reflexes normal
Labs:
 Cbc
 Liver panel
 Renal/lyte
 Lipid profile
All within her base line, except for:
 HB 12.7
 K 2.5
Hospital course…
 Pt. loss of her consciousness < 1min.
 Notice abnormal movement, not typical for convulsion
 K 2.4
 ICU transferred.
 Observation, K-replacement, ECG
Investigations???
Labs:
 Cortisol level am 313.6
 Cortisol level pm 2017.8
 ACTH 31
 DST 331
 FT4 13.5
 FT3 2.44
 T3H 0.09(SET)
 E2 142
 LH <0.07
 FSH 0.09
Brain CT:
cystic density 20*20 nm seen compressing
the pituitary gland
Brain MRI:
cystic mass lesion 2.5*1.7 cm with evidence of
hemorrhagic is seen, optic chiasma is displaced
cronaly
Finding consistent rathke cleft cyst complicated
by hemorrhagic or cystic degeneration of
pituitary macro-adenoma.
Diagnosis is…..?
ACTH-dependent Cushing’s syndrome
Harvey Williams Cushing
Cushing’s Syndrome= Hypercortisolism
Cushing's disease= Cushing's syndrome 2ry to pituitary ACTH
hypersecretion
Etiologies:
 Iatrogenic= exogenous glucocorticoid>>most
common
 Cushing’s disease= endogenous 70%
 Pituitary adenoma/hyperplasia
 Adrenal tumor 25%
 Ectopic ACTH 10%:
 Carcinoid, SCLC, medullary thyroid cancer, pheo.
Approach…
TTT..
 Mainly>>surgical resection
 Medication
 Replacement therapy lifelong.
Thank you….

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Cushing's syndrome

  • 1. Case presentation Done by: Dr. Rahma ShahBahai Medical intern
  • 2. History…  36 y.o single Saudi female k/c of HTN, T2DM and dyslipidemia  Direct admission from OPD.  Presented with lower back pain, headache and inability to walk for 3 months.  referred from KFH (Hafof) for persistent hypokalemia for further investigation.
  • 3. HPI:  3 months Hx of progressive bilateral lower limbs weakness.  Start as a simple weakness>>can’t carry her weight during standing>>become wheelchair bound.  Headache and lower back pain.  No Hx of sphincter incontinence.
  • 4. Drug Hx:  Aldactone 50 mg PO BID  Nifedipine 40 mg PO OD  Hydralazine 50 mg PO Q6H  Atorvastatin 20 mg PO OD  Labetalol 100 mg PO BID  Diamicron 90 mg PO OD
  • 5. PH:  uncontrolled HTN >10 years  Dyslipidemia+T2DM ~3month  2ry Amenorrhea ~15 yrs. His menarche @ 13>> stopped didn't seek medical advice.  No surgical Hx.
  • 6. FH:  father in good health.  Mother >>HTN  Sis1: HTN+DM  Sis 2: passed away (leukemia)  sis 3: weight gain+2ry amenorrhea
  • 7. Systemic review:  No mood changes  No dizziness  No blurred vision  excessive hair growth  acne  No respiratory or cardiac symptoms  No nausea, vomiting, diarrhea or constipation  No urinary symptoms
  • 9. Examination…  General:  Obese, round face, comfortable in the bed, not in distress.  Vitals: T 37.7 ,p 90, RR 18, BP 160/100  Skin:  hirsutism, facial plethora, acne, dorsocervical fat deposition, supraclavicular fat deposition.  Chest: clear, good air entry bilateral.  CVS: S1,S2+0  Abdomen: distended, White striae ~0.5-0.7 cm, positive bowel sound.  CNS: conscious, alert  Extremities: bruises  U.L: power 4/5, reflexes normal  L.L: muscles wasting, bruises, no edema, power 3/5, reflexes normal
  • 10. Labs:  Cbc  Liver panel  Renal/lyte  Lipid profile All within her base line, except for:  HB 12.7  K 2.5
  • 11. Hospital course…  Pt. loss of her consciousness < 1min.  Notice abnormal movement, not typical for convulsion  K 2.4  ICU transferred.  Observation, K-replacement, ECG
  • 12.
  • 14. Labs:  Cortisol level am 313.6  Cortisol level pm 2017.8  ACTH 31  DST 331  FT4 13.5  FT3 2.44  T3H 0.09(SET)  E2 142  LH <0.07  FSH 0.09
  • 15. Brain CT: cystic density 20*20 nm seen compressing the pituitary gland
  • 16.
  • 17. Brain MRI: cystic mass lesion 2.5*1.7 cm with evidence of hemorrhagic is seen, optic chiasma is displaced cronaly Finding consistent rathke cleft cyst complicated by hemorrhagic or cystic degeneration of pituitary macro-adenoma.
  • 19.
  • 21. Cushing’s Syndrome= Hypercortisolism Cushing's disease= Cushing's syndrome 2ry to pituitary ACTH hypersecretion
  • 22. Etiologies:  Iatrogenic= exogenous glucocorticoid>>most common  Cushing’s disease= endogenous 70%  Pituitary adenoma/hyperplasia  Adrenal tumor 25%  Ectopic ACTH 10%:  Carcinoid, SCLC, medullary thyroid cancer, pheo.
  • 24. TTT..  Mainly>>surgical resection  Medication  Replacement therapy lifelong.