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Primary Pleural Angiosarcoma Treated with Nivolumab and Ipilimumab: A Case Report

Primary pleural angiosarcoma (PPA) is a rare and clinically fatal pleural tumor originating from vascular endothelial cells. Herein, we presented the case of a 73-year-old man who was referred to our emergency room with complaints of right chest and back pain for a few days. Chest computed tomograph...

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Detalles Bibliográficos
Autores principales: Nakamura, Mikako, Watanabe, Kaoru, Nishimura, Taku, Yoshida, Keishi, Fukumoto, Kento, Hiyama, Noriko, Masuda, Yoshio, Morikawa, Teppei, Matsumoto, Jun, Usui, Kazuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9938394/
https://www.ncbi.nlm.nih.gov/pubmed/36820215
http://dx.doi.org/10.1159/000529447
Descripción
Sumario:Primary pleural angiosarcoma (PPA) is a rare and clinically fatal pleural tumor originating from vascular endothelial cells. Herein, we presented the case of a 73-year-old man who was referred to our emergency room with complaints of right chest and back pain for a few days. Chest computed tomography revealed massive pleural effusion and a large mass in the right chest cavity. Thoracoscopic examination demonstrated a large hemorrhagic tumor on the parietal pleura whose pathological analysis indicated PPA. The patient received immunotherapy combined with nivolumab and ipilimumab. A cycle of nivolumab and ipilimumab improved his hemorrhagic anemia and reduced the pleural effusion and tumor size. This treatment outcome suggests that nivolumab and ipilimumab comprise a vital treatment option for PPA.