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Title: Addisonian-like crisis in congenital hypopituitarism and cholestatic jaundice. Author: Lee WS, Lum LC, Harun F. Journal: Med J Malaysia; 2003 Jun; 58(2):279-81. PubMed ID: 14569750. Abstract: A six-week-old male infant was admitted for investigation of cholestasis and pale stools. He became lethargic and apnoeic with prolonged seizures after a percutaneous liver biopsy. Subsequent investigations showed conjugated hyperbilirubinaemia, elevated liver enzymes, and hypoglycaemia. The radinuclide hepatobiliary scintigraphy was non-excretory. After an operative cholangiogram, the infant developed Addisonian-like crisis with bradycardia, hypotension, respiratory distress, metabolic acidosis, hypoglycaemia, hyponatraemia, and hyperkalaemia. Blood investigations confirmed congenital hypopituitarism. Hormone replacement therapy with L-thyroxine and cortisone acetate resulted in dissolution of jaundice and the reduction of the liver size.[Abstract] [Full Text] [Related] [New Search]