Addisonian-like crisis in congenital hypopituitarism and cholestatic jaundice

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 radinuc...

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Main Authors: Lee, Way Seah, Lum, L.C., Harun, F.
Format: Article
Language:en
Published: Malaysian Medical Association 2003
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Online Access:http://eprints.um.edu.my/10921/1/Addisonian-like_crisis_in_congenital_hypopituitarism.pdf
http://eprints.um.edu.my/10921/
http://www.e-mjm.org/2003/v58n2/Congenital_Hypopituitarism.pdf
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author Lee, Way Seah
Lum, L.C.
Harun, F.
author_facet Lee, Way Seah
Lum, L.C.
Harun, F.
author_sort Lee, Way Seah
building UM Library
collection Institutional Repository
content_provider Universiti Malaya
content_source UM Research Repository
continent Asia
country Malaysia
description 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.
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spelling my.um.eprints-109212019-03-01T06:05:14Z http://eprints.um.edu.my/10921/ Addisonian-like crisis in congenital hypopituitarism and cholestatic jaundice Lee, Way Seah Lum, L.C. Harun, F. R Medicine RJ Pediatrics 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. Malaysian Medical Association 2003 Article PeerReviewed application/pdf en http://eprints.um.edu.my/10921/1/Addisonian-like_crisis_in_congenital_hypopituitarism.pdf Lee, Way Seah and Lum, L.C. and Harun, F. (2003) Addisonian-like crisis in congenital hypopituitarism and cholestatic jaundice. Medical Journal of Malaysia, 58 (2). pp. 279-281. ISSN 0300-5283, http://www.e-mjm.org/2003/v58n2/Congenital_Hypopituitarism.pdf
spellingShingle R Medicine
RJ Pediatrics
Lee, Way Seah
Lum, L.C.
Harun, F.
Addisonian-like crisis in congenital hypopituitarism and cholestatic jaundice
title Addisonian-like crisis in congenital hypopituitarism and cholestatic jaundice
title_full Addisonian-like crisis in congenital hypopituitarism and cholestatic jaundice
title_fullStr Addisonian-like crisis in congenital hypopituitarism and cholestatic jaundice
title_full_unstemmed Addisonian-like crisis in congenital hypopituitarism and cholestatic jaundice
title_short Addisonian-like crisis in congenital hypopituitarism and cholestatic jaundice
title_sort addisonian-like crisis in congenital hypopituitarism and cholestatic jaundice
topic R Medicine
RJ Pediatrics
url http://eprints.um.edu.my/10921/1/Addisonian-like_crisis_in_congenital_hypopituitarism.pdf
http://eprints.um.edu.my/10921/
http://www.e-mjm.org/2003/v58n2/Congenital_Hypopituitarism.pdf
url_provider http://eprints.um.edu.my/