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A novel immunodeficiency syndrome as a rare cause of secondary pulmonary alveolar proteinosis: A diagnosis after 5 decades

Case report of a male patient with a five-decade follow-up history in a tertiary care hospital distinguished for malabsorption syndrome, failure-to-thrive, meningitis and recurrent bacterial, fungal and mycobacterial pulmonary infections. Additionally, he developed epidermodysplasia verruciformis, s...

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Bibliografski detalji
Glavni autori: Pedro G. Ferreira, Lina Carvalho, Fernanda Gamboa
Format: Artigo
Jezik:Inglês
Izdano: Elsevier 2014-09-01
Serija:Revista Portuguesa de Pneumologia
Online pristup:http://www.sciencedirect.com/science/article/pii/S0873215914000142
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