Document Detail


Genitourinary neurofibromatosis in childhood.
MedLine Citation:
PMID:  6417345     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Neurofibromatosis in children occurs uncommonly and involvement of the bladder is exceedingly rare. The syndrome is transmitted as an autosomal dominant trait and is characterized by cutaneous pigmentation and tumors of neural crest origin. Hypertension has been documented in association with neurofibromatosis in the form of renovascular disease in children and with pheochromocytomas in adults. We report on 2 children with extensive neurofibromas of the bladder, upper tract damage and genital enlargement. One case was misdiagnosed as posterior urethral valves and the other case as clitoral hypertrophy. The literature of urogenital neurofibromatosis is reviewed with particular attention to bladder lesions, hypertension, malignant potential and treatment options.
Authors:
R C Rink; M E Mitchell
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  The Journal of urology     Volume:  130     ISSN:  0022-5347     ISO Abbreviation:  J. Urol.     Publication Date:  1983 Dec 
Date Detail:
Created Date:  1984-01-07     Completed Date:  1984-01-07     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0376374     Medline TA:  J Urol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  1176-9     Citation Subset:  AIM; IM    
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MeSH Terms
Descriptor/Qualifier:
Child, Preschool
Clitoris / pathology
Female
Humans
Hydronephrosis / etiology
Hypertension, Renovascular / etiology
Hypertrophy
Male
Neurofibromatosis 1 / complications,  radiography*
Penis / pathology
Urinary Bladder Neoplasms / complications,  radiography*

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


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