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Multiple facial angiofibromas: A cutaneous manifestation of Birt-Hogg-Dubé syndrome

Authors :
Mona Gohara
Jennifer M. McNiff
Israel Dvoretzky
Julie V. Schaffer
Sumaira Z. Aasi
Source :
Journal of the American Academy of Dermatology. 53:S108-S111
Publication Year :
2005
Publisher :
Elsevier BV, 2005.

Abstract

Birt-Hogg-Dubé syndrome (BHDS) is an uncommon autosomal dominant genodermatosis characterized by a triad of skin tumors--fibrofolliculomas, trichodiscomas, and acrochordons--together with an increased risk of renal tumors and spontaneous pneumothoraces. This report describes multiple facial angiofibromas as the predominant initial manifestation of BHDS. The patient had a total of 41 facial papules removed via shave excision, initially for diagnostic and then for therapeutic purposes; histologic evaluation revealed diagnostic features of angiofibroma in 39 lesions and fibrofolliculoma in only 2. BHDS should be considered, along with tuberous sclerosis and multiple endocrine neoplasia type 1, in the differential diagnosis of multiple facial angiofibromas, particularly when onset is in adulthood.

Details

ISSN :
01909622
Volume :
53
Database :
OpenAIRE
Journal :
Journal of the American Academy of Dermatology
Accession number :
edsair.doi.dedup.....7e886c4d4a6217aea9f25a13790e578c
Full Text :
https://doi.org/10.1016/j.jaad.2004.11.021