Intracranial Extraskeletal Mesenchymal Chondrosarcoma

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• 作者：Nishanth Sadashiva¹ ; Anil Sharma¹ ; Dhaval Shukla¹ ; Poyuran Rajalakshmi² ; Anita Mahadevan² ; Bhagavatula Indira Devi¹ ; ^{bidevidr@gmail.com" class="auth_mail" title="E-mail the corresponding author}
• 关键词：Hemangiopericytoma ; Meningeal tumor ; Meningioma ; Mesenchymal chondrosarcoma ; Mesenchymal tumor
• 刊名：World Neurosurgery
• 出版年：2016
• 出版时间：November 2016
• 年：2016
• 卷：95
• 期：Complete
• 页码：618.e1-618.e6
• 全文大小：2219 K

文摘

Intracranial extraskeletal mesenchymal chondrosarcomas (MCSs) are rare tumors accounting for <0.16% of intracranial tumors. They are usually described as occurring in the age group of 20–30 years and are commonly found in the frontoparietal region arising from the falx and surrounding dura. We describe 3 cases at varying ages, locations, and outcomes.

Case Description

A 42-year-old woman with anterior one third falx-based lesion; a 7-year-old boy with mid one third falcine lesion with hyperostosis of bone, presenting in comatose stage; and a 52-year-old woman with left posterior lateral frontal dural-based lesion are presented. Histopathology of all cases was confirmed with immunohistochemistry. All patients underwent complete excision but had varying outcomes.

Conclusions

Intracranial MCSs are rare malignant tumors with poor prognosis. Because of their rarity, it may not be considered as a differential diagnosis and it is often misdiagnosed radiologically, but the importance lies in the need of radical excision. The potential effect of postoperative radiotherapy and chemotherapy is controversial. This article sheds some light on variable prognosis of this tumor.