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...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Respir Med Case Rep
Asıl Yazarlar: Keane, Ruaidhri J., Subramaniam, Abirami, Varghese, Chithra, Jeffers, Michael, Donnelly, Seamas C.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Elsevier 2020
Konular:
Case Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7658490/
https://ncbi.nlm.nih.gov/pubmed/33209579
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.rmcr.2020.101280
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller