Lymphangioleiomyomatosis in a male

Kazuhiro Wakida, Yui Watanabe, Toshio Kumasaka, Kuniaki Seyama, Keiko Mitani, Tsubasa Hiraki, Go Kamimura, Toshiyuki Nagata, Yoshihiro Nakamura, Masami Sato

研究成果: Article査読

12 被引用数 (Scopus)

抄録

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.

本文言語English
ページ(範囲)1105-1107
ページ数3
ジャーナルAnnals of Thoracic Surgery
100
3
DOI
出版ステータスPublished - 2015 9月 1
外部発表はい

ASJC Scopus subject areas

  • 外科
  • 呼吸器内科
  • 循環器および心血管医学

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