Rare lung diseases

Abstract

Includes: Pathophysiology, classification, and lung involvement of alveolar microlithiasis and amyloidosis, hereditary haemorrhagic telangiectasia, idiopathic pulmonary haemosiderosis, Langerhans cell histiocytosis, clinical features, diagnosis, and management of lymphangioleiomyomatosis (LAM), primary ciliary dyskinesia (PCD), pathophysiology, clinical features, and diagnosis and treatment of pulmonary alveolar proteinosis (PAP), aetiology, diagnosis, management, and complications of pulmonary arteriovenous malformations (PAVMs), and recurrent respiratory papillomatosis.