Excision of massive orbital schwannoma through anterior orbital approach

Ramlal Sharma, K. Sharma, Deepti Parmar, Vineet Tanwar, S. Thakur, S. Asotra
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Abstract

Orbital schwannomas are rare, benign, slowly progressing, encapsulated tumors arising from Schwann cells of the peripheral sheath of the third, fourth, and sixth cranial nerves and ciliary ganglion. The present case is of a 32-year-old male with painless protrusion of left eye for 4 years. It was radiologically diagnosed as retro-orbital hemangioma, but histopathologic examination of the orbital tumor showed orbital schwannoma. The rarity of orbital schwannomas among orbital tumors and improvement in vision along with retained eyelid functions despite excision of a massive tumor make this a unique case.
眶前入路切除大面积眶神经鞘瘤
眼眶神经鞘瘤是一种罕见、良性、进展缓慢的包膜性肿瘤,起源于第三、第四、第六脑神经和睫状神经节外周鞘的雪旺细胞。本病例为32岁男性,左眼无痛性突出4年。影像学诊断为眼眶后血管瘤,组织病理学检查为眼眶神经鞘瘤。眼眶神经鞘瘤在眼眶肿瘤中的罕见性,以及切除巨大肿瘤后视力的改善和眼睑功能的保留,使得这是一个独特的病例。
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