Document Detail


Gingival fibromatosis and Klippel-Trénaunay-Weber syndrome. Case report.
MedLine Citation:
PMID:  7600221     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A case of a young male with the Klippel-Trénaunay-Weber syndrome is described. Typical features of hemihypertrophy, hemangiomata, macrodactyly, and macrocephaly were present. The most striking oral feature was generalized severe gingival hypertrophy confirmed histologically, ultrastructurally, and by collagen analysis. In the absence of other known systemic causes of gingival enlargement, a diagnosis of familial gingival fibromatosis in association with Klippel-Trénaunay-Weber-syndrome is concluded. The combination of gingival fibromatosis and Klippel-Trénaunay-Weber syndrome has not been reported to our knowledge, it is uncertain whether this occurrence is significant or coincidental.
Authors:
K B Hallett; A Bankier; C W Chow; J Bateman; R K Hall
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics     Volume:  79     ISSN:  1079-2104     ISO Abbreviation:  Oral Surg Oral Med Oral Pathol Oral Radiol Endod     Publication Date:  1995 May 
Date Detail:
Created Date:  1995-08-07     Completed Date:  1995-08-07     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  9508562     Medline TA:  Oral Surg Oral Med Oral Pathol Oral Radiol Endod     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  578-82     Citation Subset:  D; IM    
Affiliation:
Department of Dentistry, Royal Children's Hospital, Melbourne, Australia.
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MeSH Terms
Descriptor/Qualifier:
Child
Fibromatosis, Gingival / etiology*
Humans
Klippel-Trenaunay-Weber Syndrome / complications*
Male

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