Document Detail


Acquired hypophysitis in adolescence.
MedLine Citation:
PMID:  9388826     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Lymphocytic and granulomatous hypophysitis are rare causes of anterior pituitary dysfunction, diabetes insipidus and hyperprolactinemia. The clinical, radiographic, and laboratory features of hypophysitis in two adolescent girls are presented along with a review of the medical literature. These subjects represent the youngest cases of autoimmune (lymphocytic) and granulomatous hypophysitis reported to date. While hypophysitis remains an unusual cause of pituitary dysfunction, it may also occur in early adolescence.
Authors:
H J Heinze; B B Bercu
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Journal of pediatric endocrinology & metabolism : JPEM     Volume:  10     ISSN:  0334-018X     ISO Abbreviation:  J. Pediatr. Endocrinol. Metab.     Publication Date:    1997 May-Jun
Date Detail:
Created Date:  1997-12-19     Completed Date:  1997-12-19     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  9508900     Medline TA:  J Pediatr Endocrinol Metab     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  315-21     Citation Subset:  IM    
Affiliation:
Department of Pediatrics, Pharmacology and Therapeutics, University of South Florida College of Medicine, Tampa, USA.
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Autoimmune Diseases* / diagnosis,  therapy
Child
Female
Granulomatous Disease, Chronic / complications*,  diagnosis,  therapy
Humans
Lymphocytes / immunology
Magnetic Resonance Imaging
Pituitary Diseases / etiology*,  immunology*,  therapy
Tomography, X-Ray Computed

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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