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原发性小儿小脑胶质肉瘤。

Primary pediatric cerebellar gliosarcoma.

作者信息

Bukhari Syed Sarmad, Junaid Muhammad, Afzal Ali, Kulsoom Anisa

机构信息

Department of Neurosurgery, Aga Khan University Hospital, Karachi, Pakistan.

Department of Neurosurgery, Bahria University Medical and Dental College, Karachi, Pakistan.

出版信息

Surg Neurol Int. 2020 May 9;11:96. doi: 10.25259/SNI_274_2019. eCollection 2020.

Abstract

BACKGROUND

Primary gliosarcomas of the central nervous are rare and very few have been reported in the infratentorial compartment. Here, we describe such a lesion in a 12-year-old male.

CASE DESCRIPTION

A 12-year-old male presented with headache, ataxia, and vomiting. When Magnetic resonance studies documented a posterior fossa lesion, he underwent placement of a right ventriculoperitoneal shunt followed by a suboccipital craniectomy. The lesion proved to be a primary gliosarcoma. Unfortunately, it recurred 2 years later and required repeated resection.

CONCLUSION

Here, we reviewed the rare case of a 12-year-old male requiring shunt placement and suboccipital craniectomy for a primary gliosarcoma that recurred 2 years later.

摘要

背景

中枢神经系统原发性胶质肉瘤罕见,幕下区域报道的病例极少。在此,我们描述一名12岁男性的此类病变。

病例描述

一名12岁男性出现头痛、共济失调和呕吐症状。磁共振检查发现后颅窝有病变后,他接受了右心室 - 腹腔分流术,随后进行了枕下颅骨切除术。病变证实为原发性胶质肉瘤。不幸的是,2年后肿瘤复发,需要再次切除。

结论

在此,我们回顾了这例罕见病例,一名12岁男性因原发性胶质肉瘤接受分流术和枕下颅骨切除术,2年后肿瘤复发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b769/7265428/f5bcab0b0efa/SNI-11-96-g001.jpg

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