Document Detail


Eccrine angiomatous hamartoma: report of a case and literature review.
MedLine Citation:
PMID:  10411421     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Eccrine angiomatous hamartoma is a rare condition characterized histologically by increased numbers of eccrine structures and numerous capillary channels. Patients characteristically have a solitary, congenital nodule that may be painful and that may show hyperhidrosis. It is important to recognize this condition because it is a benign lesion for which aggressive treatment is not indicated. We report the case of a congenital eccrine angiomatous hamartoma that had a firm nodule studded with blue papules.
Authors:
T C Nakatsui; E Schloss; A Krol; A N Lin
Publication Detail:
Type:  Case Reports; Journal Article; Review    
Journal Detail:
Title:  Journal of the American Academy of Dermatology     Volume:  41     ISSN:  0190-9622     ISO Abbreviation:  J. Am. Acad. Dermatol.     Publication Date:  1999 Jul 
Date Detail:
Created Date:  1999-07-27     Completed Date:  1999-07-27     Revised Date:  2005-11-16    
Medline Journal Info:
Nlm Unique ID:  7907132     Medline TA:  J Am Acad Dermatol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  109-11     Citation Subset:  IM    
Affiliation:
Division of Dermatology and Cutaneous Sciences, University of Alberta, Edmonton.
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MeSH Terms
Descriptor/Qualifier:
Eccrine Glands / pathology*
Hamartoma / congenital,  pathology*
Hemangioma / congenital,  pathology
Humans
Infant
Male
Skin Diseases / congenital,  pathology*
Skin Neoplasms / congenital,  pathology

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


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