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...

Descripción completa

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:
Case Report
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

Internet

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

Ejemplares similares