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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Xehetasun bibliografikoak

Egile Nagusiak:	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
Formatua:	Artigo
Hizkuntza:	Inglês
Argitaratua:	Elsevier 2023-01-01
Saila:	Respiratory Medicine Case Reports
Gaiak:	Autoimmune pulmonary alveolar proteinosis Fibrotic hypersensitivity pneumonia Segmental bronchoalveolar lavage Anti-GM-CSF antibody
Sarrera elektronikoa:	http://www.sciencedirect.com/science/article/pii/S2213007123000576
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