Scholarlink

Background &amp; Introduction <p>Meningiomas are tumors that originate from non-neuroepithelial progenitor cells, meningothelial cells and the arachnoid cap cells, thus they usually appear with attachment to the dura mater. But sylvian fissure meningiomas are a rare type of meningioma that has no dural attachment.</p> Case presentation <p>A rare case of sylvian fissure meningioma is presented. The patient is a 34-year-old male with headache, and preoperative images showed a massive lesion in his right frontotemporal lobe that had no contact with the dura mater. Postoperative histopathological examination confirmed the diagnosis of a clear cell meningioma, which is a WHO grade 2 atypical meningioma and a rare subtype of meningioma that only accounts for less than 1% of all meningiomas.</p> Conclusion <p>Preoperative diagnosis of sylvian meningiomas can be challenging, leading to inappropriate operation plan and postoperative treatment. Thus, we present this case and a brief review of past cases reported, hoping to improve our understanding of the origin of meningiomas and accuracy in diagnosis of similar lesions.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

A huge cerebral parenchymal meningioma in sylvian fissure: case report and literature review

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2025年4月5日

查看全文
  • Tianyang He,
  • Zhang Zhang,
  • Xiang Wang

摘要

Background & Introduction

Meningiomas are tumors that originate from non-neuroepithelial progenitor cells, meningothelial cells and the arachnoid cap cells, thus they usually appear with attachment to the dura mater. But sylvian fissure meningiomas are a rare type of meningioma that has no dural attachment.

Case presentation

A rare case of sylvian fissure meningioma is presented. The patient is a 34-year-old male with headache, and preoperative images showed a massive lesion in his right frontotemporal lobe that had no contact with the dura mater. Postoperative histopathological examination confirmed the diagnosis of a clear cell meningioma, which is a WHO grade 2 atypical meningioma and a rare subtype of meningioma that only accounts for less than 1% of all meningiomas.

Conclusion

Preoperative diagnosis of sylvian meningiomas can be challenging, leading to inappropriate operation plan and postoperative treatment. Thus, we present this case and a brief review of past cases reported, hoping to improve our understanding of the origin of meningiomas and accuracy in diagnosis of similar lesions.