Arpaci Rabia B, Kara Tuba, Vayisoğlu Yusuf, Ozgur Anil, Ozcan Cengiz
Department of Pathology, School of Medicine, Mersin University, Turkey.
J Craniofac Surg. 2012 Jul;23(4):1194-6. doi: 10.1097/SCS.0b013e31824e6d09.
Glomangiopericytoma (sinonasal-type hemangiopericytoma) is a rare tumor arising from the periyctes surrounding capillaries and accounts for less than 0.5% of all sinonasal tumors. It falls within the category of borderline and low-malignant-potential soft tissue tumors of the nose and paranasal sinuses. It is defined by the World Health Organization as a sinonasal tumor demonstrating a perivascular myoid phenotype. It was noted that when this lesion arose in the nasal cavity, it tended to behave in a more indolent fashion than its soft tissue counterpart, suggesting that sinonasal hemangiopericytomas represented a distinct entity. We report a case of a 68-year-old female patient diagnosed with glomangiopericytoma arising in the left sinonasal cavity and discussed the condition in terms of differential diagnosis.
血管外皮细胞瘤(鼻窦型血管外皮细胞瘤)是一种罕见的肿瘤,起源于围绕毛细血管的周细胞,占所有鼻窦肿瘤的比例不到0.5%。它属于鼻腔和鼻窦交界性及低恶性潜能软组织肿瘤范畴。世界卫生组织将其定义为表现出血管周围肌样表型的鼻窦肿瘤。值得注意的是,当这种病变发生在鼻腔时,其行为往往比软组织同类病变更为惰性,这表明鼻窦血管外皮细胞瘤是一种独特的实体。我们报告一例68岁女性患者,诊断为左鼻窦腔血管外皮细胞瘤,并从鉴别诊断的角度对该病例进行了讨论。