ty -jour a2 -tura，A。A2 -Koizumi，T。Au -Abu -Zaid，Ahmed Au -Mohammed -Mohammed，Shamayel PY-2013 DA -2013/06/13 ti-一名63岁的绅士中的主要胸膜hateosarcomaSP -974567 VL -2013 AB-主要胸膜血管肉瘤极为罕见。截至2010年，文献中仅记录了大约50个病例报告。在本文中，我们报告了一位63岁的绅士的案例，他呈现了3个月的右侧胸痛，呼吸困难和屈曲的历史。胸部X射线表现出双侧胸膜积液，部分双骨肺炎肺炎症。超声引导的胸腔穿刺术显示出流血和渗出性胸膜液。细胞学检查对恶性细胞阴性。腹部对比增强的计算机断层扫描（CT）扫描显示两个右diaphragmargmatic胸膜肿块。全身正电子发射断层扫描/计算机断层扫描（PET/CT）扫描显示两种多代代谢氟脱氧葡萄糖 - （FDG-）抗透射性胸膜病变。进行了CT引导的针核活检，组织病理学检查表明，肿瘤细胞主要生长在具有焦点区域的薄片中，暗示着由细胞学上恶性上皮细胞衬砌的血管空间。 Immunohistochemical analysis showed strong positivity for vimentin, CD31, CD68, and Fli-1 markers. The overall pathological and immunohistochemical features supported the diagnosis of epithelioid angiosarcoma. The patient was scheduled for surgery in three weeks. Unfortunately, the patient died after one week after discharge secondary to pulseless ventricular tachycardia arrest followed by asystole. Moreover, we also present a brief literature review on pleural angiosarcoma. SN - 2090-6846 UR - https://doi.org/10.1155/2013/974567 DO - 10.1155/2013/974567 JF - Case Reports in Pulmonology PB - Hindawi Publishing Corporation KW - ER -