Cargando…
Pulmonary capillary hemangiomatosis-predominant vasculopathy in a patient with rheumatoid arthritis-associated interstitial lung disease: An autopsy report
Pulmonary capillary hemangiomatosis (PCH) is a rare cause of pulmonary hypertension (PH) associated with poor prognosis. Clinically, it is characterized by severe hypoxemia, centrilobular ground-glass opacities on computed tomography, and pulmonary congestion triggered by pulmonary vasodilating ther...
Autores principales: | Nakamura, Junichi, Tsujino, Ichizo, Yamamoto, Gaku, Nakaya, Toshitaka, Takahashi, Kei, Kimura, Hirokazu, Sato, Takahiro, Watanabe, Taku, Nakagawa, Shimpei, Otsuka, Noriyuki, Ohira, Hiroshi, Konno, Satoshi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7527749/ https://www.ncbi.nlm.nih.gov/pubmed/33024689 http://dx.doi.org/10.1016/j.rmcr.2020.101215 |
Ejemplares similares
-
Autopsy study of pulmonary capillary hemangiomatosis with inflammatory cell
infiltration into the myocardium
por: Omori, Taku, et al.
Publicado: (2020) -
An Autopsy Case of Pulmonary Capillary Hemangiomatosis with an Electron Microscopy Study
por: Kobayashi, Hiroshi, et al.
Publicado: (2019) -
Familial Pulmonary Capillary Hemangiomatosis Early in Life
por: Wirbelauer, Johannes, et al.
Publicado: (2011) -
Pulmonary capillary hemangiomatosis: a lesson learned
por: Guzman, Samuel, et al.
Publicado: (2019) -
Broad and heterogeneous vasculopathy in pulmonary fibrosis and emphysema with pulmonary hypertension
por: Sato, Takahiro, et al.
Publicado: (2013)