Silicosis complicated with autoimmune pulmonary alveolar proteinosis caused by long-term dust inhalation during construction of bridge pier columns: A case report
Pulmonary alveolar proteinosis (PAP) is characterized by the accumulation of surfactant material in alveoli. Few aPAP cases with a history of dust inhalation show both paves stone-like changes and micronodules in the chest CT scan. We present a 52-year-old male patient withsilicosis complicated with...
Saved in:
| Main Authors: | Jie Jiang, YouMing Zhu, Tao Jiang, TingTing Hu, YiLing Gan |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2024-11-01
|
| Series: | Heliyon |
| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2405844024163554 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Whole Lung Lavage in Autoimmune Pulmonary Alveolar Proteinosis: Unique Challenges in a Resource‐Limited Setting
by: Ashesh Dhungana, et al.
Published: (2024-11-01) -
Autoimmune pulmonary alveolar proteinosis developed during treatment for systemic sclerosis: a case report
by: Tomoki Kozono, et al.
Published: (2025-01-01) -
Case report: Infantile pulmonary alveolar proteinosis associated with cytosolic isoleucyl-tRNA synthetase deficiency
by: Jie Wu, et al.
Published: (2025-01-01) -
Case Report: Innovative anesthetic approaches for whole lung lavage in an infant with pulmonary alveolar proteinosis
by: Jiaxiang Chen, et al.
Published: (2025-01-01) -
Fast-Track Extubation in a Patient Undergoing Whole Lung Lavage: A Case Report
by: Gade Sandeep, et al.
Published: (2025-01-01)