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Secondary Pulmonary Alveolar Proteinosis Associated with Primary Myelofibrosis and Ruxolitinib Treatment: An Autopsy Case

Pulmonary alveolar proteinosis (PAP) is an uncommon lung disorder characterized by the excessive accumulation of surfactant-derived lipoproteins in the pulmonary alveoli and terminal bronchiole. Secondary PAP associated with primary myelofibrosis (PMF) is extremely rare, and to our knowledge, no aut...

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Detalles Bibliográficos
Autores principales: Sugiura, Hiroyuki, Nishimori, Hisakazu, Nishii, Kazuya, Toji, Tomohiro, Fujii, Keiko, Fujii, Nobuharu, Matsuoka, Ken-ichi, Nakata, Koh, Kiura, Katsuyuki, Maeda, Yoshinobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7492123/
https://www.ncbi.nlm.nih.gov/pubmed/32448830
http://dx.doi.org/10.2169/internalmedicine.4082-19

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