Diagnostic and Therapeutic Dilemmas in Recurrent Pulmonary Alveolar Proteinosis After Bilateral Lung Transplantation
ABSTRACT Pulmonary alveolar proteinosis (PAP) is a rare granulocyte–macrophage colony‐stimulating factor (GM‐CSF) dependent lung disease treated primarily with whole‐lung lavage (WLL); recurrence after lung transplantation is uncommon and poorly characterised. We present a 73‐year‐old Hispanic man w...
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| Autori principali: | , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Wiley
2026-06-01
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| Serie: | Respirology Case Reports |
| Soggetti: | |
| Accesso online: | https://doi.org/10.1002/rcr2.70653 |
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