Document Detail


Macrodactyly: report of eight cases and review of the literature.
MedLine Citation:
PMID:  10990574     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Congenital enlargement of one or several digits of the hands or feet (macrodactyly) is a rare disorder. A considerable proportion of the patients with this condition are referred to dermatology departments. The majority of the cases reported in the literature represent hamartomas with combined hypertrophy of several, predominantly lipomatous, soft tissue components and overgrowth of bone. The differential diagnosis includes Klippel-Trenaunay-Weber syndrome, neurofibromatosis, Milroy disease, and Proteus syndrome. We describe eight cases of congenital macrodactyly, discuss the findings, and propose a simple clinicopathologic terminology.
Authors:
S Krengel; A Fustes-Morales; D Carrasco; M Vázquez; C Durán-McKinster; R Ruiz-Maldonado
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Publication Detail:
Type:  Case Reports; Journal Article; Review    
Journal Detail:
Title:  Pediatric dermatology     Volume:  17     ISSN:  0736-8046     ISO Abbreviation:  Pediatr Dermatol     Publication Date:    2000 Jul-Aug
Date Detail:
Created Date:  2000-10-02     Completed Date:  2000-10-02     Revised Date:  2009-03-03    
Medline Journal Info:
Nlm Unique ID:  8406799     Medline TA:  Pediatr Dermatol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  270-6     Citation Subset:  IM    
Affiliation:
Departments of Pediatric Dermatology, Pathology, and Outpatient Department, National Institute of Pediatrics, Mexico City, Mexico.
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MeSH Terms
Descriptor/Qualifier:
Adolescent
Child
Child, Preschool
Female
Fingers / abnormalities*
Humans
Infant
Limb Deformities, Congenital / pathology*
Male
Syndactyly
Toes / abnormalities*
Comments/Corrections
Comment In:
Pediatr Dermatol. 2001 Jul-Aug;18(4):364-5   [PMID:  11576419 ]

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


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