Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1782217910265053184 |
---|---|
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. |
format | Online Article Text |
id | pubmed-3229063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Korean Dermatological Association; The Korean Society for Investigative Dermatology |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT shinwonwoong birthoggdubesyndromeararecaseinkoreaconfirmedbygeneticanalysis AT baekyoosang birthoggdubesyndromeararecaseinkoreaconfirmedbygeneticanalysis AT ohtaeseok birthoggdubesyndromeararecaseinkoreaconfirmedbygeneticanalysis AT heoyoungsoo birthoggdubesyndromeararecaseinkoreaconfirmedbygeneticanalysis AT sonsoobin birthoggdubesyndromeararecaseinkoreaconfirmedbygeneticanalysis AT ohchilhwan birthoggdubesyndromeararecaseinkoreaconfirmedbygeneticanalysis AT songhaejun birthoggdubesyndromeararecaseinkoreaconfirmedbygeneticanalysis |