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岩尖部巨大骨内神经鞘瘤伴瘤内出血。

Large Intraosseous Schwannoma in Petrous Apex Presenting with Intratumoral Hemorrhage.

机构信息

Department of Neurosurgery, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.

Department of Neurosurgery, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima, Japan.

出版信息

World Neurosurg. 2019 Nov;131:53-57. doi: 10.1016/j.wneu.2019.07.179. Epub 2019 Jul 31.

DOI:10.1016/j.wneu.2019.07.179
PMID:31376556
Abstract

BACKGROUND

Intracranial schwannomas are rarely confined to the skull. We here report a large schwannoma localized in the petrous apex that presented with intratumoral hemorrhage.

CASE DESCRIPTION

A 35-year-old woman with mild hearing disturbance and ear fullness underwent computed tomography scan and magnetic resonance imaging, which demonstrated a tumor accompanied with intratumoral hematoma in the right petrous apex. Bone marrow was totally destroyed, but the bone cortex was relatively preserved. Pathologic specimen showed that the tumor was composed of proliferation of elongated neoplastic cells and positive for S-100 protein. It showed a nuclear palisading pattern, compatible with schwannoma. The lack of any cranial nerve signs and relative preservation of canals through which cranial nerves pass suggested the neurilemma cells surrounded vessels or mismigrated fetal neurilemma cells in the petrous apex as origin of the tumor. Benign nature of the tumor and total disappearance of the symptoms, supposedly due to the spontaneous absorption of the hematoma, made the patient choose a wait-and-watch approach. Magnetic resonance imaging studied 7 years after the diagnosis showed significant decrease of the tumor volume and disappearance of the hematoma.

CONCLUSIONS

Although it is a large intraosseous schwannoma in the petrous apex, it has a benign nature, its size is reduced due to the hematoma absorption, and the patient is asymptomatic. We observed the patients for 7 years after the diagnosis.

摘要

背景

颅内神经鞘瘤很少局限于颅骨。我们在此报告一例位于岩尖的大型神经鞘瘤,表现为肿瘤内出血。

病例描述

一名 35 岁女性,有轻度听力障碍和耳闷感,行计算机断层扫描和磁共振成像检查,显示右侧岩尖有肿瘤伴肿瘤内血肿。骨髓完全破坏,但骨皮质相对保存。病理标本显示肿瘤由增生的长形肿瘤细胞组成,S-100 蛋白阳性。呈核栅状排列,符合神经鞘瘤。缺乏任何颅神经体征,以及通过颅神经的管道相对保存,提示肿瘤起源于围绕血管的神经鞘细胞或在岩尖错位的胎儿神经鞘细胞。肿瘤的良性性质和症状的完全消失,可能是由于血肿的自发吸收,使患者选择了观察等待的方法。诊断后 7 年的磁共振成像研究显示肿瘤体积显著缩小,血肿消失。

结论

尽管这是一个位于岩尖的大型骨内神经鞘瘤,但它具有良性性质,由于血肿吸收,其大小减小,且患者无症状。我们在诊断后观察了患者 7 年。

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