Junuzović Dzelaludin, Kulovac Benjamin, Aganović Damir, Prcić Alden, Babić Mirsad, Bajramović Senad
Klinika za Urologiju, Klinicki Centar Univerziteta u Sarajevu.
Med Arh. 2006;60(6 Suppl 1):50-3.
Haemangiopericytoma is an uncommon tumour of vascular origin. We report a case of one of the rarer sites of this tumour in man: pelvic paravesical site. We report case of 47 years old man with pelvic hemangiopericytoma and discuss imaging studies and pathohystological findings. Although modern imaging techniques have provided useful information concerning the hypervascular and clearly demarcated appearance of this tumour which displaces but does not invade adjacent organs, its diagnosis can only be established by histology. Its degree of malignancy and its invasive potential are unclear. The risk of local recurrence and metastases in more than one half of cases justifies wide surgical excision, possibly combined with adjuvant radiotherapy, and long-term follow-up. That is to say, that hemangiopericytoma malignum pelvis is the very rare sites of this tumour and till now it is not reported in Bosnia and Herzegovina.
血管外皮细胞瘤是一种罕见的血管源性肿瘤。我们报告了该肿瘤在人体中较为罕见的一个部位的病例：盆腔膀胱旁部位。我们报告了一名47岁患有盆腔血管外皮细胞瘤的男性病例，并讨论了影像学研究和病理组织学发现。尽管现代成像技术提供了有关该肿瘤血管丰富且边界清晰的外观的有用信息，该肿瘤推移但不侵犯相邻器官，但其诊断只能通过组织学来确定。其恶性程度和侵袭潜力尚不清楚。超过一半的病例存在局部复发和转移的风险，这证明了广泛手术切除的合理性，可能联合辅助放疗，并进行长期随访。也就是说，盆腔恶性血管外皮细胞瘤是该肿瘤非常罕见的部位，到目前为止在波斯尼亚和黑塞哥维那尚未有报道。
