A case of development of autoimmune pulmonary alveolar proteinosis during the treatment of hypersensitivity pneumonitis

Herein, we report the case of a 73-year-old woman with an occupational history of plaster grinding who developed autoimmune pulmonary alveolar proteinosis (PAP) during the treatment of fibrotic hypersensitivity pneumonitis with steroids and immunosuppressive drugs. Based on the changes in computed t...

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Autori principali:	Maki Asami-Noyama, Kosuke Ito, Misa Harada, Yukari Hisamoto, Yoshie Kunihiro, Eiji Ikeda, Tasuku Yamamoto, Junki Suizu, Ayumi Fukatsu, Syuichiro Ohata, Yoriyuki Murata, Keiji Oishi, Yoshikazu Yamaji, Nobutaka Edakuni, Tomoyuki Kakugawa, Tsunahiko Hirano, Kazuto Matsunaga
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Elsevier 2023-01-01
Serie:	Respiratory Medicine Case Reports
Soggetti:	Autoimmune pulmonary alveolar proteinosis Fibrotic hypersensitivity pneumonia Segmental bronchoalveolar lavage Anti-GM-CSF antibody
Accesso online:	http://www.sciencedirect.com/science/article/pii/S2213007123000576
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