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内耳道神经胶质神经错构瘤:一种伪装成前庭神经鞘瘤的罕见肿块。

Internal Auditory Canal Glioneural Hamartoma: A Rare Mass Masquerading as a Vestibular Schwannoma.

作者信息

Li Daphne, Shanker Rachyl, Borys Ewa, Leonetti John P, Anderson Douglas E

机构信息

Neurosurgery, Loyola University Medical Center, Maywood, USA.

Pediatric Neurosurgery, Advocate Lutheran General Hospital, Park Ridge, USA.

出版信息

Cureus. 2023 Apr 10;15(4):e37361. doi: 10.7759/cureus.37361. eCollection 2023 Apr.

Abstract

Glioneural hamartomas are exceedingly rare lesions. When localized to the internal auditory canal (IAC), they can cause symptoms referrable to seventh and eighth cranial nerve compression. Here, the authors present a rare case of an IAC glioneural hamartoma. A 57-year-old male presented for evaluation of presumed  schwannomas found on work-up of dizziness and progressive right-sided hearing loss. Surgical intervention pursued progressive symptoms and new onset headaches. The patient underwent uncomplicated retrosigmoid craniectomy for gross total resection. Histopathological evaluation revealed a glioneural hamartoma. A MEDLINE database search used the terms' cerebellopontine angle' OR 'internal auditory canal' AND 'hamartoma' OR 'heterotopia'. Clinicopathological characteristics and outcomes of the present case were compared to those in the literature. The literature review yielded nine articles describing 11 cases (eight females, three males; median age 40 years, range 11-71) of intracanalicular glioneural hamartomas. Patients most commonly presented with hearing loss and were presumed to have a diagnosis of vestibular schwannoma before histologic diagnosis. Glioneural hamartomas are rare lesions that may be found in the IAC. Although benign, they may be safely resected for cranial nerve function preservation goals with a low risk of recurrence.

摘要

神经胶质神经错构瘤是极为罕见的病变。当局限于内耳道(IAC)时,它们可导致与第七和第八颅神经受压相关的症状。在此,作者报告了一例罕见的内耳道神经胶质神经错构瘤病例。一名57岁男性因在头晕和进行性右侧听力损失检查中发现疑似神经鞘瘤而前来评估。手术干预针对进行性症状和新发头痛。患者接受了乙状窦后开颅手术,实现了肿瘤全切,且手术过程顺利。组织病理学评估显示为神经胶质神经错构瘤。通过使用“小脑脑桥角”或“内耳道”以及“错构瘤”或“异位”等术语在MEDLINE数据库中进行检索。将本病例的临床病理特征和结果与文献中的情况进行了比较。文献综述得出9篇文章,描述了11例(8名女性,3名男性;中位年龄40岁,范围11 - 71岁)内耳道神经胶质神经错构瘤病例。患者最常见的表现为听力损失,在组织学诊断之前多被推测为前庭神经鞘瘤。神经胶质神经错构瘤是罕见的病变,可能在内耳道中发现。尽管是良性的,但为了保留颅神经功能,可对其进行安全切除,复发风险较低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f791/10170578/691604f6c769/cureus-0015-00000037361-i01.jpg

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