A Rare Case of Autoimmune Pulmonary Alveolar Proteinosis Developing During the Course of Eosinophilic Granulomatosis With Polyangiitis

A Rare Case of Autoimmune Pulmonary Alveolar Proteinosis Developing During the Course of Eosinophilic Granulomatosis With Polyangiitis

ABSTRACT Eosinophilic granulomatosis with polyangiitis (EGPA) is an anti‐neutrophil cytoplasmic antibody (ANCA)‐associated vasculitis characterised by asthma, eosinophilia, and systemic inflammation, often involving the lungs. We present the case of a 47‐year‐old woman with EGPA who developed progre...

Full description

Saved in:
Bibliographic Details
Main Authors: Yoichi Dotake, Kentaro Tanaka, Shiro Fujisaki, Kenichi Shimobaba, Hirotoshi Kuroiwa, Midori Satomura, Hiromi Matsuyama, Koichi Takagi, Hideo Mitsuyama, Hiromasa Inoue
Format: Article
Language:English
Published: Wiley 2025-05-01
Series:Respirology Case Reports
Subjects:
asthma
eosinophilic granulomatosis with polyangiitis
pulmonary alveolar proteinosis
Online Access:https://doi.org/10.1002/rcr2.70219
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

https://doi.org/10.1002/rcr2.70219

Similar Items