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外生脑干胶质瘤成功手术治疗:酷似桥小脑角肿瘤病例报告及文献复习。

Successful Surgery of Exophytic Brainstem Glioma Mimicking Cerebellar-Pontine Angle Tumor: Case Report and Review of Literature.

机构信息

Neurosurgical Department, Erlangen University Clinic, Neuroradiological Department, University Hospital Erlangen, Germany.

Neurosurgical Department, Erlangen University Clinic, Neuroradiological Department, University Hospital Erlangen, Germany.

出版信息

World Neurosurg. 2019 Aug;128:202-205. doi: 10.1016/j.wneu.2019.05.053. Epub 2019 May 14.

Abstract

BACKGROUND

Nontectal plate exophytic brainstem gliomas with pilocytic histology are rare and occur mainly in children. Because of their eloquent location, therapy usually consists of bioptic histologic verification and radiotherapy in case of progression.

CASE DESCRIPTION

We report on a 43-year-old patient who presented with intermittent tinnitus and reduced hearing in his left ear, as well as a slight left-sided ataxia. Magnetic resonance imaging revealed a left-sided solid cystic cerebellar-pontine angle (CPA) tumor completely obliterating the CPA. Radiologically, a solid cystic vestibular schwannoma was diagnosed. Intraoperatively, a glossy-grayish, intensively bleeding tumor without any capsule or delineation to the brainstem or cranial nerves was resected using electrophysiologic monitoring. Postoperative histology revealed a pilocytic astrocytoma. Three months postoperatively, hearing was preserved (pure tone average-35 dB) and ataxia was equal to what it was preoperatively, gradually becoming better. Postoperative magnetic resonance scans demonstrated a complete resection of the tumor with completely restored brainstem contours.

CONCLUSIONS

Exophytic brainstem gliomas may occur in the CPA and mimic vestibular schwannoma. Complete resection even with preserved hearing without neurologic deterioration may be feasible.

摘要

背景

非室管膜外生性脑干胶质瘤伴毛细胞型组织学特征较为罕见,主要发生于儿童。由于其位于重要部位,治疗通常包括活检以明确组织学特征,以及在进展时进行放疗。

病例描述

我们报告了一位 43 岁的患者,他因间歇性耳鸣和左耳听力下降,以及轻微的左侧共济失调而就诊。磁共振成像显示左侧实性囊性桥小脑角(CPA)肿瘤完全占据了 CPA。影像学诊断为实性囊性前庭神经鞘瘤。术中,在电生理监测下切除了一个无包膜、与脑干或颅神经无界限的光滑、灰白色、明显出血的肿瘤。术后组织学检查显示为毛细胞型星形细胞瘤。术后 3 个月,听力得以保留(纯音平均 35dB),且术前的共济失调程度与术后相同,逐渐好转。术后磁共振扫描显示肿瘤完全切除,脑干轮廓完全恢复。

结论

外生性脑干胶质瘤可发生于 CPA 并模拟前庭神经鞘瘤。即使在保留听力且神经功能无恶化的情况下,完全切除肿瘤也是可行的。

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