Initial presentation of Pulmonary Langerhans cell histiocytosis as recurrent spontaneous pneumothoraces

Pulmonary Langerhans cell histiocytosis (PLCH) is a rare cystic lung disease. The natural history is often unpredictable making it difficult to diagnose. We report a 63-year-old male with dyspnoea, chronic cough and recurrent respiratory tract infections, who developed progressive multifocal cystic...

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Bibliographic Details
Main Authors: Ruaidhri J. Keane, Abirami Subramaniam, Chithra Varghese, Michael Jeffers, Seamas C. Donnelly
Format: Article
Language:English
Published: Elsevier 2020-01-01
Series:Respiratory Medicine Case Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2213007120304949