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放射诱导的间变性室管膜瘤酷似颅底脑膜瘤:一例报告。

Radiation-induced anaplastic ependymoma mimicking a skull base meningioma: A case report.

作者信息

Spallone Aldo, Marchione Pasquale, DI Capua Mario, Belvisi Daniele

机构信息

Section of Neurosurgery, Department of Clinical Neurosciences, Neurological Centre of Latium, Rome I-00178, Italy; Department of Biomedicine, University of Rome 'Tor Vergata', Rome I-00173, Italy.

Section of Neurosurgery, Department of Clinical Neurosciences, Neurological Centre of Latium, Rome I-00178, Italy.

出版信息

Exp Ther Med. 2016 Feb;11(2):455-457. doi: 10.3892/etm.2015.2945. Epub 2015 Dec 16.

Abstract

The present study describes the case of a 63-year-old woman presenting with headache, dizziness and vomiting due to a an ovoid mass in the left pre-bulbar cistern, apparently arising from the lower clivus and the foramen magnum. The clinical history revealed the subtotal removal of a right cerebellar low-grade glioma 15 years previously and subsequent conventional 60-Gy radiotherapy. Notably, following gross total resection, histopathological examination showed microscopic features that resulted in a diagnosis of anaplastic ependymoma. The patient underwent surgery to remove the mass and post-operative chemotherapy with temozolomide. A progressive improvement of neurological signs and symptoms was observed during the postoperative course. At the 6-month follow-up, the patient was free from clinical and radiological recurrence. The unusual features of this rare secondary brain tumor were the extrassial location in the posterior fossa, the unusual age-associated location of the histological subtype and the fact that it closely mimicked a skull-base meningioma.

摘要

本研究描述了一名63岁女性的病例,该患者因左桥前池的卵形肿块出现头痛、头晕和呕吐症状,该肿块显然起源于斜坡下部和枕骨大孔。临床病史显示,15年前曾对右侧小脑低级别胶质瘤进行次全切除,并随后进行了常规的60 Gy放疗。值得注意的是,在肿瘤全切除后,组织病理学检查显示出的微观特征诊断为间变性室管膜瘤。患者接受了手术切除肿块,并术后使用替莫唑胺进行化疗。术后过程中观察到神经体征和症状逐渐改善。在6个月的随访中,患者无临床和影像学复发。这种罕见的继发性脑肿瘤的不寻常特征包括位于后颅窝的颅外位置、组织学亚型与年龄相关的不寻常位置,以及它与颅底脑膜瘤极为相似的事实。

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