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

Author:

Nakamura Mikako,Watanabe Kaoru,Nishimura Taku,Yoshida Keishi,Fukumoto KentoORCID,Hiyama Noriko,Masuda Yoshio,Morikawa Teppei,Matsumoto Jun,Usui KazuhiroORCID

Abstract

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.

Publisher

S. Karger AG

Subject

Oncology

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