Optic nerve sheath schwannoma: illustrative case.

George Rudd, Amir Kaywan Aftahy, Bernhard Meyer, Maria Wostrack
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Abstract

Background: In this case report, the authors discuss the diagnosis and treatment of a rare primary optic nerve sheath schwannoma (ONSS). Typically, intracranial schwannomas arise from the vestibular division of cranial nerve VIII and seldom cranial nerves V and VII. This case underscores the need for further documentation of ONSS to better understand its origins, refine diagnostic approaches, and optimize management strategies to enable earlier detection and better outcomes for patients' vision.

Observations: The authors present the case of a 36-year-old patient who presented via an ophthalmologist due to visual loss in the left eye. She was initially treated for optic neuritis before further deterioration prompted repeat imaging, demonstrating a left extraorbital lesion distal to the optic chiasm. The patient underwent a complete resection of the lesion via pterional craniotomy in July 2024.

Lessons: The authors report the 17th case of ONSS in the literature. Despite the optic nerve's usual myelination pattern, these tumors can form, likely originating from ectopic Schwann cells or perioptic sympathetic fibers. Resection via a pterional approach enabled complete removal without postoperative complications. Because of the rarity of ONSS, further study is essential to enhance diagnosis, treatment, and surgical strategies. https://thejns.org/doi/10.3171/CASE25156.

视神经鞘神经鞘瘤:说明性病例。
背景:在这个病例报告中,作者讨论了罕见的原发性视神经鞘神经鞘瘤(ONSS)的诊断和治疗。通常,颅内神经鞘瘤起源于颅神经VIII的前庭分裂,很少发生颅神经V和颅神经VII。该病例强调需要进一步记录ONSS,以更好地了解其起源,改进诊断方法,优化管理策略,以便早期发现并改善患者视力。观察:作者提出的情况下,一个36岁的病人谁提出了通过眼科医生由于视力丧失在左眼。她最初因视神经炎接受治疗,后来病情进一步恶化,重复影像学检查,发现左眶外病变远至视交叉。患者于2024年7月通过翼点开颅手术完全切除病变。总结:本文报告了文献中第17例ONSS病例。尽管视神经通常有髓鞘形成,但这些肿瘤可能起源于异位雪旺细胞或视周交感神经纤维。经翼位入路切除可完全切除,无术后并发症。由于ONSS的罕见性,进一步的研究是必要的,以提高诊断,治疗和手术策略。https://thejns.org/doi/10.3171/CASE25156。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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