| Literature DB >> 26028485 |
Chinatsu Nishida1, Kazuhiro Yatera2, Kei Yamasaki1, Ryo Torii1, Yukiko Kawanami1, Toshinori Kawanami1, Hiroshi Ishimoto1, Ryo Shibuya3, Masaru Takenaka4, Sohusuke Yamada5, Takahiko Kasai6, Fumihiro Tanaka4, Hiroshi Mukae1.
Abstract
A 65-year-old Japanese woman was introduced to our hospital for an examination of multiple pulmonary cystic lesions and a pulmonary nodule in the left lower lobe. She had a smoking history of 25 pack-years, and her two younger brothers had suffered from pneumothorax; one of them additionally had lung cancer with pulmonary multiple cystic lesions. A surgical biopsy specimen obtained from her left lower lobe revealed adenocarcinoma surrounded by a single epithelial layer that was covered with collagen fibers. The pathological features were compatible with the findings of the cystic lesions in the patients with Birt-Hogg-Dubé syndrome (BHDS). A diagnosis of BHDS was eventually made according to the detection of a folliculin gene mutation. This is the first report of a possible familial case of BHDS complicated with primary lung cancer. We herein reviewed the previously reported cases of BHDS with lung cancer and other tumors and discussed a potential mechanism of tumorigenesis and carcinogenesis in the lung in the patients with BHDS.Entities:
Keywords: Birt–Hogg–Dubé syndrome; Carcinogenesis; Folliculin; Lung cancer; Pulmonary cyst
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Year: 2015 PMID: 26028485 DOI: 10.1016/j.rmed.2015.05.005
Source DB: PubMed Journal: Respir Med ISSN: 0954-6111 Impact factor: 3.415