Literature DB >> 19198241

[A case of pulmonary alveolar proteinosis presenting with peripheral ground-glass opacitiy].

Takahiro Haga1, Norio Kasamatsu, Takeshi Kobayashi, Masahiko Shibata, Takashi Ogasawara, Ikko Hashizume.   

Abstract

A 65-year-old asymptomatic nonsmoker woman was found to have bilateral ground glass opacities in subpleural areas. The bronchoalveolar lavage fluid had a light-milky appearance and transbronchial lung biopsy revealed alveolar filling with PAS-positive acellular material. The patient was given a diagnosis of pulmonary alveolar proteinosis (PAP). Chest CT 18 months later showed no changes in the shadows. It may be possible to follow asymptomatic PAP with patchy peripheral air-space disease without treatment.

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Year:  2009        PMID: 19198241

Source DB:  PubMed          Journal:  Nihon Kokyuki Gakkai Zasshi        ISSN: 1343-3490


  2 in total

1.  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.  A young non-immunocompromised woman with diffuse alveolar opacities.

Authors:  Prem Parkash Gupta; Manish Verma; Dipti Agarwal; Sanjay Kumar; Atulya Atreja
Journal:  Lung India       Date:  2010-10
  2 in total

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