Birt-hogg-dubé syndrome, a rare case in Korea confirmed by genetic analysis

Ann Dermatol. 2011 Oct;23(Suppl 2):S193-6. doi: 10.5021/ad.2011.23.S2.S193. Epub 2011 Oct 31.

Abstract

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.

Keywords: Birt-Hogg-Dubé syndrome; Fibrofolliculoma; Folliculin.

Publication types

  • Case Reports