Literature DB >> 19687589

A Japanese family with multiple lung cysts and recurrent pneumothorax: a possibility of Birt-Hogg-Dubé syndrome.

Hiroshi Ishii1, Hiroaki Oka, Yuka Amemiya, Atsuko Iwata, Satoshi Otani, Kenji Kishi, Ryo Shirai, Issei Tokimatsu, Katsunobu Kawahara, Jun-ichi Kadota.   

Abstract

We herein report a Japanese family lineage, possibly demonstrating Birt-Hogg-Dubé (BHD) syndrome. A 29-year-old nonsmoking woman was admitted to our hospital due to spontaneous pneumothorax. A chest CT showed multiple lung cysts, and breast cancer was simultaneously detected that needed priority surgical treatment. In the family history, the patient's father and half brother also experienced recurrent pneumothorax, and both had similar findings in their chest CT. In a genetic analysis of her half brother, the mutation of the BHD gene was identified. BHD syndrome is a rare autosomal and dominantly inherited disorder, which has three characteristics: multiple lung cysts that may be associated with pneumothorax, skin fibrofolliculomas, and renal neoplasm. For multiple-cystic disease of the lungs with an unknown etiology, or pneumothorax, as seen in a family history, it is necessary to consider the possibility of BHD syndrome.

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Year:  2009        PMID: 19687589     DOI: 10.2169/internalmedicine.48.2144

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


  7 in total

1.  Clinical and genetic spectrum of Birt-Hogg-Dube syndrome patients in whom pneumothorax and/or multiple lung cysts are the presenting feature.

Authors:  Makiko Kunogi; Masatoshi Kurihara; Takako Shigihara Ikegami; Toshiyuki Kobayashi; Noriko Shindo; Toshio Kumasaka; Yoko Gunji; Mika Kikkawa; Shin-ichiro Iwakami; Okio Hino; Kazuhisa Takahashi; Kuniaki Seyama
Journal:  J Med Genet       Date:  2010-04       Impact factor: 6.318

2.  Breast cancer in a patient with Birt-Hogg-Dubé syndrome (BHDS) with dramatic response to neoadjuvant chemotherapy.

Authors:  Vivek Yadala; Hassaan Jafri; Mary T Legenza; Maria Tirona
Journal:  BMJ Case Rep       Date:  2020-02-04

3.  Characterization of pulmonary cysts in Birt-Hogg-Dubé syndrome: histopathological and morphometric analysis of 229 pulmonary cysts from 50 unrelated patients.

Authors:  Toshio Kumasaka; Takuo Hayashi; Keiko Mitani; Hideyuki Kataoka; Mika Kikkawa; Kazunori Tobino; Etsuko Kobayashi; Yoko Gunji; Makiko Kunogi; Masatoshi Kurihara; Kuniaki Seyama
Journal:  Histopathology       Date:  2014-03-04       Impact factor: 5.087

4.  Recurrent renal cancer in Birt-Hogg-Dubé syndrome: A case report.

Authors:  Hammad Ather; Nida Zahid
Journal:  Int J Surg Case Rep       Date:  2017-11-28

5.  A Case of Birt-Hogg-Dubé (BHD) Syndrome Harboring a Novel Folliculin (FLCN) Gene Mutation.

Authors:  Takuro Yukawa; Takuya Fukazawa; Masakazu Yoshida; Ichiro Morita; Katsuya Kato; Yasumasa Monobe; Mitsuko Furuya; Yoshio Naomoto
Journal:  Am J Case Rep       Date:  2016-10-26

6.  Two Japanese cases of birt-hogg-dubé syndrome with pulmonary cysts, fibrofolliculomas, and renal cell carcinomas.

Authors:  Yukako Murakami; Mari Wataya-Kaneda; Mari Tanaka; Aya Takahashi; Akira Tsujimura; Koji Inoue; Norio Nonomura; Ichiro Katayama
Journal:  Case Rep Dermatol       Date:  2014-02-07

7.  FLCN-regulated miRNAs suppressed reparative response in cells and pulmonary lesions of Birt-Hogg-Dubé syndrome.

Authors:  Haiyan Min; Dehua Ma; Wei Zou; Yongzheng Wu; Yibing Ding; Chengchu Zhu; Anqi Lin; Shiyu Song; Qiao Liang; Baofu Chen; Bin Zhang; Yueming Wan; Minhua Ye; Yanqing Pan; Yanting Wen; Long Yi; Qian Gao
Journal:  Thorax       Date:  2020-03-17       Impact factor: 9.139

  7 in total

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