Document Detail


WDHA syndrome caused by pheochromocytoma: report of a case.
MedLine Citation:
PMID:  657943     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A case in which a pheochromocytoma secreted vasoactive intestinal peptide, causing WDHA syndrome, is reported. The patient, a 43-year-old woman, was seen because of intractable watery diarrhea, hypokalemia and weight loss. She was found to have a mass in the right adrenal area. Preoperatively, vasoactive intestinal peptide levels were elevated, and the diagnosis of WDHA syndrome was entertained. Exploratory laparotomy revealed a tumor of the right adrenal gland, measuring 15 x 15 cm, which was resected. Histologic examination revealed it to be a pheochromocytoma. Postoperatively, vasoactive intestinal peptide returned to normal. The patient had complete remission of symptoms, and has remained well since.
Authors:
M K Matta; J J Prorok; H D Trimpi; J A Sheets; J J Stasik; I T Khubchandani
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Diseases of the colon and rectum     Volume:  21     ISSN:  0012-3706     ISO Abbreviation:  Dis. Colon Rectum     Publication Date:    1978 May-Jun
Date Detail:
Created Date:  1978-08-14     Completed Date:  1978-08-14     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  0372764     Medline TA:  Dis Colon Rectum     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  297-301     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Achlorhydria / etiology*
Adrenal Gland Neoplasms / complications*,  diagnosis
Adult
Diarrhea / etiology*
Female
Humans
Hypokalemia / etiology*
Pheochromocytoma / complications*,  diagnosis
Syndrome
Ultrasonography

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


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