| Literature DB >> 26354644 |
Kazuhiro Wakida1, Yui Watanabe2, Toshio Kumasaka3, Kuniaki Seyama4, Keiko Mitani5, Tsubasa Hiraki6, Go Kamimura1, Toshiyuki Nagata1, Yoshihiro Nakamura1, Masami Sato1.
Abstract
We report a 17-year-old male with a histopathologic diagnosis of lymphangioleiomyomatosis after surgery for a pneumothorax. In general, lymphangioleiomyomatosis has been considered a female-specific disease. However, there are a few lymphangioleiomyomatosis cases reported in males, and our patient is the youngest case reported. Spontaneous pneumothorax occurs most commonly in males in their late teens and early twenties. Histopathologic diagnosis cannot always be performed in young males with pneumothorax. However, simple diagnosis should be avoided, and lymphangioleiomyomatosis should be considered as an underlying disease. This remarkable case provides new and valuable clinical insights into young male pneumothorax.Entities:
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Year: 2015 PMID: 26354644 DOI: 10.1016/j.athoracsur.2014.11.069
Source DB: PubMed Journal: Ann Thorac Surg ISSN: 0003-4975 Impact factor: 4.330