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小儿多房性三叉神经鞘瘤:病例说明

Pediatric multicompartmental trigeminal schwannoma: illustrative case.

作者信息

Landry Alexander P, Ye Vincent C, Vaughan Kerry A, Drake James M, Dirks Peter B, Cusimano Michael D

机构信息

Divison of Neurosurgery, University of Toronto, Toronto, Ontario, Canada.

Division of Neurosurgery, Hospital for Sick Children, Toronto, Ontario, Canada; and.

出版信息

J Neurosurg Case Lessons. 2021 May 17;1(20):CASE2171. doi: 10.3171/CASE2171.

Abstract

BACKGROUND

Trigeminal schwannoma (TS) is an uncommon and histologically benign intracranial lesion that can involve any segment of the fifth cranial nerve. Given its often impressive size at diagnosis and frequent involvement of critical neurovascular structures of the skull base, it represents a challenging entity to treat. Pediatric TS is particularly rare and presents unique challenges. Similarly, tumors with extension into multiple compartments (e.g., middle cranial fossa, posterior cranial fossa, extracranial spaces) are notoriously difficult to treat surgically. Combined or staged surgical approaches are typically required to address them, with radiosurgical treatment as an adjunct.

OBSERVATIONS

The authors presented the unusual case of a 9-year-old boy with a large, recurrent multicompartmental TS involving Meckel's cave, the cerebellopontine angle, and the infratemporal fossa. Near-total resection was achieved using a frontotemporal-orbitozygomatic craniotomy with a combined interdural and extradural approach.

LESSONS

The case report adds to the current literature on multicompartmental TSs in children and their management. The authors also provided a simplified classification of TS that can be generalized to other skull base tumors. Given a lack of precedent, the authors intended to add to the discussion regarding surgical management of these rare and challenging skull base lesions.

摘要

背景

三叉神经鞘瘤(TS)是一种罕见的组织学上为良性的颅内病变,可累及第五颅神经的任何节段。鉴于其在诊断时通常体积较大,且常累及颅底关键神经血管结构,它是一种具有挑战性的治疗实体。小儿TS尤为罕见,且存在独特的挑战。同样,肿瘤延伸至多个腔隙(如中颅窝、后颅窝、颅外间隙)的情况在手术治疗上 notoriously difficult(此处疑为“极其困难”,原文有误)。通常需要联合或分期手术方法来处理,放射外科治疗作为辅助手段。

观察结果

作者介绍了一例不同寻常的病例,一名9岁男孩患有巨大的复发性多腔隙TS,累及梅克尔腔、桥小脑角和颞下窝。采用额颞眶颧开颅术结合硬膜内和硬膜外联合入路实现了近全切除。

经验教训

该病例报告丰富了当前关于儿童多腔隙TS及其治疗的文献。作者还提供了一种可推广至其他颅底肿瘤的TS简化分类。鉴于缺乏先例,作者旨在增加关于这些罕见且具有挑战性的颅底病变手术治疗的讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/895c/9245852/a7ad52341ed7/CASE2171f1.jpg

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