Osanai T, Kanazawa T, Nakamura K, Tsushima T, Kimura M, Onodera K
Second Department of Internal Medicine, Hirosaki University School of Medicine, Japan.
Arch Pathol Lab Med. 1994 May;118(5):575-7.
We describe a 35-year-old man with a primary cystic mediastinal hemangiopericytoma who presented with the complaint of progressive dysphagia for 6 months. The computed tomography and magnetic resonance imaging findings revealed that a well-defined, fluid-filled mass (measuring approximately 10 x 10 cm) was located posterior to the heart and inferior to the carina of the bronchus. Tumor puncture showed translucent yellow fluid with normal concentrations of carcinoembryonic antigen, squamous cell carcinoma-related antigen, and carbohydrate antigen 19-9 and a high concentration of carbohydrate antigen 125. After removal of the tumor, microscopic examination revealed a malignant hemangiopericytoma. To our knowledge, this is the first case of a primary mediastinal hemangiopericytoma with cystic formation. Moreover, we showed the specific biochemical findings of the cystic fluid that were useful for differentiation from other cystic mediastinal tumors.
我们描述了一名35岁男性,患有原发性囊性纵隔血管外皮细胞瘤,因进行性吞咽困难6个月前来就诊。计算机断层扫描和磁共振成像结果显示,一个边界清晰、充满液体的肿块(大小约为10×10厘米)位于心脏后方、支气管隆突下方。肿瘤穿刺显示为半透明黄色液体,癌胚抗原、鳞状细胞癌相关抗原和糖类抗原19-9浓度正常,而糖类抗原125浓度较高。肿瘤切除后,显微镜检查显示为恶性血管外皮细胞瘤。据我们所知,这是首例伴有囊性形成的原发性纵隔血管外皮细胞瘤。此外,我们展示了囊液的特定生化检查结果,这些结果有助于与其他囊性纵隔肿瘤相鉴别。