Pulmonary cysts of birt-hogg-dubé syndrome: A clinicopathologic and immunohistochemical study of 9 families

Mitsuko Furuya, Reiko Tanaka, Shunsuke Koga, Yasushi Yatabe, Hiroko Gotoda, Seiji Takagi, Yung Hsiang Hsu, Takeshi Fujii, Akira Okada, Naoto Kuroda, Suzuko Moritani, Hideki Mizuno, Yoji Nagashima, Kiyotaka Nagahama, Kenzo Hiroshima, Ichiro Yoshino, Fumio Nomura, Ichiro Aoki, Yukio Nakatani

Research output: Contribution to journalArticlepeer-review


Birt-Hogg-Dubé (BHD) syndrome is an autosomal dominant disorder characterized by fibrofolliculomas, renal tumors, and pulmonary cysts with recurrent pneumothorax. Multiple pulmonary cysts and pneumothorax are the key signs for diagnosing BHD syndrome. The pathologic features of BHD pulmonary cysts, however, are poorly understood. This disorder is caused by mutations in the gene that encodes folliculin (FLCN). FLCN is regarded as a tumor suppressor; it mediates cellular activities by interacting with the mammalian target of rapamycin (mTOR). In this study, we investigated the lungs of 11 patients from 9 BHD families. The majority of patients consulting doctors were women between 30 and 60 years of age who had pulmonary cysts and repeated pneumothoraces. Genomic DNA testing revealed 5 different mutation patterns. Histopathologic examination found that the inner surface of cysts was lined by epithelial cells, sometimes with a predominance of type II pneumocyte-like cuboidal cells. The cysts occasionally contained internal septa consisting of alveolar walls or showed an "alveoli within an alveolus" pattern. The cells constituting the cysts stained positive for phospho-S6 ribosomal protein expression, suggesting activation of the mTOR pathway. Although BHD pulmonary cysts are frequently misdiagnosed as nonspecific cystic diseases, they are distinctly different in histopathology from other bullous changes. Mechanical stress such as rupture and postrupture remodeling allows mesothelial invagination and fibrosis. Such modified BHD pulmonary cysts are virtually indistinguishable from nonspecific blebs and bullae. We propose a new insight, namely, that the BHD syndrome-associated pulmonary cyst may be considered a hamartoma-like cystic alveolar formation associated with deranged mTOR signaling.

Original languageEnglish (US)
Pages (from-to)589-600
Number of pages12
JournalAmerican Journal of Surgical Pathology
Issue number4
StatePublished - Apr 2012


  • Birt-Hogg-Dubé syndrome
  • folliculin
  • mTOR
  • pulmonary cysts
  • renal tumors

ASJC Scopus subject areas

  • Anatomy
  • Surgery
  • Pathology and Forensic Medicine


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