Document Detail


Pathology of MEN-1: morphology, clinicopathologic correlations and tumour development.
MedLine Citation:
PMID:  9681843     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Multiple endocrine neoplasia type 1 (MEN-1) is an inherited syndrome which is characterized by the occurrence of neoplastic lesions in the parathyroids, the pancreas, duodenum, anterior pituitary and, less commonly, also in the stomach, thymus and lung. Its genetic defect has recently been identified and appears to involve a new type of tumour suppressor gene called mu on chromosome 11q13. In this overview, we will summarize the morphological features of the MEN-1 phenotype, discuss its clinicopathologic profile and prognosis and outline the recent findings on the molecular pathology of this syndrome.
Authors:
P Komminoth; P U Heitz; G Klöppel
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Publication Detail:
Type:  Journal Article; Review    
Journal Detail:
Title:  Journal of internal medicine     Volume:  243     ISSN:  0954-6820     ISO Abbreviation:  J. Intern. Med.     Publication Date:  1998 Jun 
Date Detail:
Created Date:  1998-08-13     Completed Date:  1998-08-13     Revised Date:  2005-11-16    
Medline Journal Info:
Nlm Unique ID:  8904841     Medline TA:  J Intern Med     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  455-64     Citation Subset:  IM    
Affiliation:
Department of Pathology, University of Zürich, Switzerland.
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MeSH Terms
Descriptor/Qualifier:
Diagnosis, Differential
Humans
Multiple Endocrine Neoplasia Type 1 / diagnosis*,  genetics*,  pathology
Prognosis

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


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