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Birt-Hogg-Dubé Syndrome, a Rare Case in Korea Confirmed by Genetic Analysis

Simple benign tumors can present as part of a syndrome with substantial mortality. Fibrofolliculomas are benign skin tumors most often associated with the Birt-Hogg-Dubé syndrome (BHDS). The most life-threatening complication of this syndrome is renal cancer and other major features include multiple...

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Autores principales: Shin, Won Woong, Baek, Yoo Sang, Oh, Tae Seok, Heo, Young Soo, Son, Soo Bin, Oh, Chil Hwan, Song, Hae Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Dermatological Association; The Korean Society for Investigative Dermatology 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3229063/
https://www.ncbi.nlm.nih.gov/pubmed/22148048
http://dx.doi.org/10.5021/ad.2011.23.S2.S193
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author Shin, Won Woong
Baek, Yoo Sang
Oh, Tae Seok
Heo, Young Soo
Son, Soo Bin
Oh, Chil Hwan
Song, Hae Jun
author_facet Shin, Won Woong
Baek, Yoo Sang
Oh, Tae Seok
Heo, Young Soo
Son, Soo Bin
Oh, Chil Hwan
Song, Hae Jun
author_sort Shin, Won Woong
collection PubMed
description Simple benign tumors can present as part of a syndrome with substantial mortality. Fibrofolliculomas are benign skin tumors most often associated with the Birt-Hogg-Dubé syndrome (BHDS). The most life-threatening complication of this syndrome is renal cancer and other major features include multiple lung cysts and spontaneous pneumothorax. We present the case of a 54 year-old man with multiple flesh-colored papules on his face confirmed histologically as fibrofolliculomas. He had a history of recurrent pneumothorax and chest computed tomography showed multiple lung cysts. To confirm the diagnosis of BHDS, we conducted gene analysis that revealed a single nucleotide duplication in the folliculin (FLCN) gene (Exon 11, C.1285dupC). BHDS confirmed by the FLCN gene mutation is rarely reported in Korea. Appropriate investigation is recommended whenever a patient with benign skin tumors is encountered.
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spelling pubmed-32290632011-12-06 Birt-Hogg-Dubé Syndrome, a Rare Case in Korea Confirmed by Genetic Analysis Shin, Won Woong Baek, Yoo Sang Oh, Tae Seok Heo, Young Soo Son, Soo Bin Oh, Chil Hwan Song, Hae Jun Ann Dermatol Case Report Simple benign tumors can present as part of a syndrome with substantial mortality. Fibrofolliculomas are benign skin tumors most often associated with the Birt-Hogg-Dubé syndrome (BHDS). The most life-threatening complication of this syndrome is renal cancer and other major features include multiple lung cysts and spontaneous pneumothorax. We present the case of a 54 year-old man with multiple flesh-colored papules on his face confirmed histologically as fibrofolliculomas. He had a history of recurrent pneumothorax and chest computed tomography showed multiple lung cysts. To confirm the diagnosis of BHDS, we conducted gene analysis that revealed a single nucleotide duplication in the folliculin (FLCN) gene (Exon 11, C.1285dupC). BHDS confirmed by the FLCN gene mutation is rarely reported in Korea. Appropriate investigation is recommended whenever a patient with benign skin tumors is encountered. Korean Dermatological Association; The Korean Society for Investigative Dermatology 2011-10 2011-10-31 /pmc/articles/PMC3229063/ /pubmed/22148048 http://dx.doi.org/10.5021/ad.2011.23.S2.S193 Text en Copyright © 2011 Korean Dermatological Association; The Korean Society for Investigative Dermatology 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 (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Shin, Won Woong
Baek, Yoo Sang
Oh, Tae Seok
Heo, Young Soo
Son, Soo Bin
Oh, Chil Hwan
Song, Hae Jun
Birt-Hogg-Dubé Syndrome, a Rare Case in Korea Confirmed by Genetic Analysis
title Birt-Hogg-Dubé Syndrome, a Rare Case in Korea Confirmed by Genetic Analysis
title_full Birt-Hogg-Dubé Syndrome, a Rare Case in Korea Confirmed by Genetic Analysis
title_fullStr Birt-Hogg-Dubé Syndrome, a Rare Case in Korea Confirmed by Genetic Analysis
title_full_unstemmed Birt-Hogg-Dubé Syndrome, a Rare Case in Korea Confirmed by Genetic Analysis
title_short Birt-Hogg-Dubé Syndrome, a Rare Case in Korea Confirmed by Genetic Analysis
title_sort birt-hogg-dubé syndrome, a rare case in korea confirmed by genetic analysis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3229063/
https://www.ncbi.nlm.nih.gov/pubmed/22148048
http://dx.doi.org/10.5021/ad.2011.23.S2.S193
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