Literature DB >> 18781111

[A case of idiopathic pulmonary alveolar proteinosis with multiple localized ground-glass opacities].

Hirokazu Taniguchi1, Hitoshi Abo, Masayoshi Touge, Hideki Shinnou, Hideki Miyazawa, Hirofumi Noto, Akio Uchiyama, Atsuo Miwa, Shoetsu Shimura, Saburo Izumi.   

Abstract

A 58-year-old Japanese female consulted our staff with multiple localized ground-glass opacities in chest CT. She underwent video assisted thoracoscopic surgery for diagnosis. Histopathologic finding from surgery specimen in one of ground-glass opacities revealed bronchioloalveolar carcinoma. Six months later, we performed second video assisted thoracoscopic surgery, and histopathologic finding of all other ground-glass opacities revealed pulmonary alveolar proteinosis. Serum anti GM-CSF antibody elevated, and she was diagnosed as having idiopathic pulmonary alveolar proteinosis. A case of idiopathic pulmonary alveolar proteinosis presenting multiple localized ground-glass opacities is rare. And, differentiating ground-glass opacities of pulmonary alveolar proteinosis and bronchioloalveolar carcinoma by chest CT is difficult.

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Year:  2008        PMID: 18781111

Source DB:  PubMed          Journal:  Arerugi        ISSN: 0021-4884


  2 in total

1.  Atypical pulmonary alveolar proteinosis presenting as a mixed nodular ground-glass opacity with focal mucinosis mimicking lung cancer.

Authors:  Tsutomu Shinohara; Hiroyuki Hino; Shino Imanishi; Keishi Naruse; Yuji Ohtsuki; Fumitaka Ogushi
Journal:  J Thorac Dis       Date:  2018-09       Impact factor: 2.895

2.  Autoimmune pulmonary alveolar proteinosis with features similar to nonspecific interstitial pneumonia.

Authors:  Koki Fujii; Hideyuki Takeshima; Taku Nishimura; Toshio Sakatani; Yoshio Masuda; Teppei Morikawa; Kazuhiro Usui
Journal:  Respir Med Case Rep       Date:  2022-02-03
  2 in total

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