Document Detail


Multiple occurrence of osteochondromas in dysplasia epiphysealis hemimelica.
MedLine Citation:
PMID:  10853915     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Dysplasia epiphysealis hemimelica was defined by Trevor (1950) as a rare congenital growth disorder of the tarsus and of the epiphysis of the long bone. In this report, a rare case of dysplasia epiphysealis hemimelica associated with multiple extraskeletal osteochondromas is presented. Although different modes of expression of the same pathologic process have been suggested for dysplasia epiphysealis hemimelica and osteochondroma, the biological feature of cartilaginous overgrowth in the skeletal system still seems unclear.
Authors:
M Takagi; Y Kiyoshige; A Ishikawa; T Ogino
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Archives of orthopaedic and trauma surgery     Volume:  120     ISSN:  0936-8051     ISO Abbreviation:  Arch Orthop Trauma Surg     Publication Date:  2000  
Date Detail:
Created Date:  2000-10-19     Completed Date:  2000-10-19     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  9011043     Medline TA:  Arch Orthop Trauma Surg     Country:  GERMANY    
Other Details:
Languages:  eng     Pagination:  358-60     Citation Subset:  IM    
Affiliation:
Department of Orthopaedic Surgery, Yamagata University School of Medicine, Japan.
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MeSH Terms
Descriptor/Qualifier:
Child
Epiphyses / abnormalities*,  pathology,  radiography
Female
Femoral Neoplasms / pathology,  radiography*,  surgery
Humans
Knee Joint / pathology,  radiography,  surgery
Osteochondrodysplasias / pathology,  radiography*,  surgery
Osteochondromatosis / pathology,  radiography*,  surgery
Soft Tissue Neoplasms / pathology,  radiography*,  surgery

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


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