Case report: Fibrotic interstitial lung disease as the initial manifestation of hereditary pulmonary alveolar proteinosis caused by CSF2RB mutation

A 50-year-old male was admitted to the hospital with a 3-year history of dyspnea and cough. Chest high-resolution computed tomography (HRCT) did not show typical features of pulmonary alveolar proteinosis (PAP), but rather atypical features of interstitial lung disease with fibrosis. The diagnosis o...

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Hauptverfasser:	Qiuhong Li, Huikang Xie, Manhui Li, Kebin Cheng
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	Frontiers Media S.A. 2024-01-01
Schriftenreihe:	Frontiers in Pharmacology
Schlagworte:	CSF2RB fibrotic interstitial lung disease chest high-resolution computed tomography mutation pulmonary alveolar proteinosis
Online-Zugang:	https://www.frontiersin.org/articles/10.3389/fphar.2023.1252193/full
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