Takano K, Suzuki N, Saito H, Ishibashi K, Nitta K, Hoshi E, Kondo K
Nihon Geka Gakkai Zasshi. 1985 Aug;86(8):959-65.
Hemangiopericytoma is a rare capillary tumor that was first described and named by Stout and Murray in 1942. A case of hemangiopericytoma in the pelvic retroperitoneum is reported. The patient, a 57 year old man, was admitted because of dysuria. He underwent extirpation of the tumor with the rectum by low anterior resection. The pathological diagnosis was malignant hemangiopericytoma, and Adriamycin was administered to prevent recurrence or metastasis. He has been free from any recurrence or metastasis for the last eight months. Twenty cases of hemangiopericytoma in the retroperitoneum including our case, were collected from Japanese literature and reviews. Hemangiopericytoma, especially in the retroperitoneal space, should be regarded as a highly malignant tumor. Early aggressive therapy and long term follow up are recommended because the tumor characteristically produces late local recurrence and metastasis.
血管外皮细胞瘤是一种罕见的毛细血管肿瘤,于1942年由斯托特和默里首次描述并命名。本文报告一例盆腔腹膜后血管外皮细胞瘤。患者为一名57岁男性,因排尿困难入院。他接受了低位前切除术,将肿瘤与直肠一并切除。病理诊断为恶性血管外皮细胞瘤,并给予阿霉素以预防复发或转移。在过去的八个月里,他没有出现任何复发或转移。我们从日本文献和综述中收集了包括我们病例在内的20例腹膜后血管外皮细胞瘤。血管外皮细胞瘤,尤其是位于腹膜后间隙的,应被视为高度恶性肿瘤。由于该肿瘤具有典型的晚期局部复发和转移的特点,建议早期积极治疗并进行长期随访。