Literature DB >> 26354644

Lymphangioleiomyomatosis in a Male.

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.
Copyright © 2015 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.

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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


  2 in total

1.  Two Kinds of Cystic Lung Lesions with Pulmonary Lymphangioleiomyomatosis in a Male.

Authors:  Sumitaka Yamanaka; Teruaki Mizobuchi; Masatoshi Kurihara
Journal:  Ann Thorac Cardiovasc Surg       Date:  2016-06-27       Impact factor: 1.520

2.  A Systematic Review of Lymphangioleiomyomatosis on Diagnosis and Molecular Mechanism.

Authors:  Xiaotong Dong; Lvcheng Jin; Ailan Wang; Liping Wu; Xintong Fan; Qian Hou; Tianbao Li; Ruilian Zhao; Yunxiang Zhang
Journal:  Biomed Res Int       Date:  2021-02-10       Impact factor: 3.411

  2 in total

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