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Birt-Hogg-Dubé syndrome

A 45-year-old woman with a history of renal carcinoma was observed for facial, cervical and truncal flesh-colored papules. Relatives had similar skin findings and a brother had repeated episodes of pneumothorax. The computerized tomography scan revealed multiple cysts on both lungs. A skin biopsy re...

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Detalles Bibliográficos
Autores principales: Lencastre, André, Ponte, Pedro, Apetato, Margarida, Nunes, Luis, Lestre, Sara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876010/
https://www.ncbi.nlm.nih.gov/pubmed/24346920
http://dx.doi.org/10.1590/abd1806-4841.20132199
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author Lencastre, André
Ponte, Pedro
Apetato, Margarida
Nunes, Luis
Lestre, Sara
author_facet Lencastre, André
Ponte, Pedro
Apetato, Margarida
Nunes, Luis
Lestre, Sara
author_sort Lencastre, André
collection PubMed
description A 45-year-old woman with a history of renal carcinoma was observed for facial, cervical and truncal flesh-colored papules. Relatives had similar skin findings and a brother had repeated episodes of pneumothorax. The computerized tomography scan revealed multiple cysts on both lungs. A skin biopsy revealed a perifollicular fibroma. The clinical diagnosis of Birt-Hogg-Dubé syndrome (BHDS) was corroborated by identification of a novel frameshift c.573delGAinsT (p.G191fsX31) mutation in heterozygosity on exon 6 of the folliculin gene. The presence of multiple and typical benign hair follicle tumors highlights the role of the dermatologist in the diagnosis of this rare genodermatosis that is associated with an increased risk of renal cell cancer and pulmonary cysts, warranting personal and familial follow-up and counseling.
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spelling pubmed-38760102014-01-08 Birt-Hogg-Dubé syndrome Lencastre, André Ponte, Pedro Apetato, Margarida Nunes, Luis Lestre, Sara An Bras Dermatol Case Report A 45-year-old woman with a history of renal carcinoma was observed for facial, cervical and truncal flesh-colored papules. Relatives had similar skin findings and a brother had repeated episodes of pneumothorax. The computerized tomography scan revealed multiple cysts on both lungs. A skin biopsy revealed a perifollicular fibroma. The clinical diagnosis of Birt-Hogg-Dubé syndrome (BHDS) was corroborated by identification of a novel frameshift c.573delGAinsT (p.G191fsX31) mutation in heterozygosity on exon 6 of the folliculin gene. The presence of multiple and typical benign hair follicle tumors highlights the role of the dermatologist in the diagnosis of this rare genodermatosis that is associated with an increased risk of renal cell cancer and pulmonary cysts, warranting personal and familial follow-up and counseling. Sociedade Brasileira de Dermatologia 2013 /pmc/articles/PMC3876010/ /pubmed/24346920 http://dx.doi.org/10.1590/abd1806-4841.20132199 Text en ©2013 by Anais Brasileiros de Dermatologia http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Lencastre, André
Ponte, Pedro
Apetato, Margarida
Nunes, Luis
Lestre, Sara
Birt-Hogg-Dubé syndrome
title Birt-Hogg-Dubé syndrome
title_full Birt-Hogg-Dubé syndrome
title_fullStr Birt-Hogg-Dubé syndrome
title_full_unstemmed Birt-Hogg-Dubé syndrome
title_short Birt-Hogg-Dubé syndrome
title_sort birt-hogg-dubé syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876010/
https://www.ncbi.nlm.nih.gov/pubmed/24346920
http://dx.doi.org/10.1590/abd1806-4841.20132199
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