一种联合手术入路治疗中鼻眼眶球结膜细胞瘤

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
A. Labouchère, Cécile De Sandre, M. Broome, A. Reinhard, A. Louvrier
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引用次数: 0

摘要

摘要血管外皮细胞瘤是一种罕见的鼻窦肿瘤,复发率高。鼻内窥镜手术是切除此类肿瘤的经典技术。我们在此报告一例鼻窦血管外皮细胞瘤伴眼眶扩张,在文献中少见。一名50岁女性因9个月前出现的右侧鼻部无痛性肿胀而转介至我院,自首次就诊后逐渐增大。磁共振成像(MRI)显示肿瘤(18 × 25 × 37 mm)以右侧筛细胞为中心,伴有邻近的鼻骨侵蚀和右侧眼眶侵犯。术前栓塞后,采用联合手术入路(内窥镜和经鼻窦额路)切除肿瘤。根据组织病理学检查结果,诊断为肾小球外皮细胞瘤。患者在一周后出院,并进行了平静的长期随访。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Combined Surgical Approach for the Treatment of a Sino-Naso-Orbital Glomangiopericytoma
Glomangiopericytomas are a rare type of sinonasal tumors with high relapse rates. Endoscopic sinus surgery is the classical technique to remove such tumors. Here we report a case of sinonasal glomangiopericytoma with orbital extension, infrequently described in the literature. A 50 year-old woman was referred to our hospital because of a right paranasal painless swelling, which appeared 9 months ago and was slowly increasing in size since her first visit. A Magnetic Resonance Imaging (MRI) revealed a tumor (18 × 25 × 37 mm) centered on the right ethmoidal cells, with adjacent nasal bone erosion and a right orbital invasion. The tumor was removed with a combined surgical approach (endoscopic and trans-sinusal frontal approach) after pre-surgical embolization. Based on the results of the histopathological examination, the diagnosis of a glomangiopericytoma was confirmed. The patient was discharged after one week, and an uneventful long-term follow-up.
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