Document Detail


Cowden's syndrome with Lhermitte-Duclos disease.
MedLine Citation:
PMID:  16455548     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Cowden's syndrome (CS) is a rare autosomal dominant condition featuring multiple hamartomas, often with mucocutaneous lesions, goitre, breast cancer, gastrointestinal polyps or even Lhermitte-Duclos disease (LDD). In this article we report the case of a 34-year-old man who was diagnosed with LDD. Subsequent examinations also revealed manifestations of CS, i.e. macrocephaly, thyroid nodules and gastrointestinal polyps.
Authors:
T Boonpipattanapong; N Phuenpathom; W Mitarnun
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Publication Detail:
Type:  Case Reports; Journal Article; Review    
Journal Detail:
Title:  British journal of neurosurgery     Volume:  19     ISSN:  0268-8697     ISO Abbreviation:  Br J Neurosurg     Publication Date:  2005 Aug 
Date Detail:
Created Date:  2006-02-03     Completed Date:  2006-05-25     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8800054     Medline TA:  Br J Neurosurg     Country:  England    
Other Details:
Languages:  eng     Pagination:  361-5     Citation Subset:  IM    
Affiliation:
Department of Surgery, Faculty of Medicine, Prince of Songkla University, Songkla, Thailand. yean178@hotmail.com
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MeSH Terms
Descriptor/Qualifier:
Adult
Cerebellar Neoplasms / diagnosis*,  pathology
Ganglioglioma / diagnosis*,  pathology
Hamartoma Syndrome, Multiple / diagnosis*
Humans
Magnetic Resonance Imaging
Male

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


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