Marar Maher, Mohammad Saad, Abdulraheem Ahmad, Hammad Munther, Al Hayek Sa'ed
School of Medicine, The University of Jordan, Amman 11942, Jordan.
Department of Medicine, Medstar Washington Hospital Center, Washington, DC 20010, USA.
Radiol Case Rep. 2025 Jun 9;20(9):4257-4261. doi: 10.1016/j.radcr.2025.05.023. eCollection 2025 Sep.
Primary cardiac angiosarcoma is an extremely rare and aggressive tumor that originates from the endothelial lining of cardiac blood vessels. We report a case of a 48-year-old man with history of military burn pit exposure, who presented with shortness of breath, cough, and hemoptysis. He was treated as a case of pneumonia, later he developed a diffuse pulmonary hemorrhage, and the etiology of his symptoms was found to be cardiac angiosarcoma with lung involvement. This case highlights the important clinical, radiological, and pathological characteristics of a rare cancer that commonly spreads to the lungs, urging healthcare providers to keep it in mind when diagnosing hemoptysis and pulmonary hemorrhage.
原发性心脏血管肉瘤是一种极其罕见且侵袭性强的肿瘤,起源于心脏血管的内皮衬里。我们报告一例48岁男性病例,他有军事燃烧坑暴露史,出现呼吸急促、咳嗽和咯血症状。他最初被当作肺炎治疗,后来发展为弥漫性肺出血,其症状的病因被发现是心脏血管肉瘤伴肺部受累。该病例突出了这种罕见癌症的重要临床、放射学和病理学特征,这种癌症通常会扩散至肺部,促使医疗服务提供者在诊断咯血和肺出血时牢记这一情况。