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

• المؤلفون الرئيسيون: Qiuhong Li (مؤلف), Huikang Xie (مؤلف), Manhui Li (مؤلف), Kebin Cheng (مؤلف)
• التنسيق: كتاب
• منشور في: Frontiers Media S.A., 2024-01-01T00:00:00Z.
• الموضوعات: article
• الوصول للمادة أونلاين: Connect to this object online.

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...