Case report: Intradural-extramedullary cervical spine clear cell meningioma mimicking a schwannoma in a child

Clear cell meningioma (CCM) is an exceedingly rare subtype of meningioma, with spinal occurrences being even more uncommon. It predominantly affects children and is characterized by a high recurrence rate and poor prognosis, posing significant challenges for clinical treatment. Currently, gross total resection (GTR) is the best approach to reduce recurrence and improve prognosis in these patients. However, detailed descriptions of intraoperative findings, particularly for intraspinal cervical CCM, are scarce in the literature. Here, we report a rare case in which the upper cervical spinal CCM mimicked a schwannoma, detailing the surgical treatment strategy and prognosis. Additionally, we analyzed all previously reported cases of spinal CCM to investigate the clinical characteristics, optimal treatment strategies, and prognostic factors, which may be of particular interest to neurosurgeons.

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Publication Details

Journal
Frontiers in Oncology
Published
2025-01-10
DOI
https://doi.org/10.3389/fonc.2024.1505141
Citations
1
Primary Topic
Neurofibromatosis and Schwannoma Cases
Type
article
Field-Weighted Citation Impact
1.39
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article

Case report: Intradural-extramedullary cervical spine clear cell meningioma mimicking a schwannoma in a child

Bin Xu, Chongxi Xu, Jianguo Xu, Seidu A. Richard et al.
1 citations
Frontiers in Oncology
Neurofibromatosis and Schwannoma Cases
1.39
article

Case report: Intradural-extramedullary cervical spine clear cell meningioma mimicking a schwannoma in a child

Bin Xu, Chongxi Xu, Jianguo Xu, Seidu A. Richard, Jiaxi Wang, Yong‐Liang Jiang, Hao Li, Xiang Yang
article en
1 citations

Abstract

Clear cell meningioma (CCM) is an exceedingly rare subtype of meningioma, with spinal occurrences being even more uncommon. It predominantly affects children and is characterized by a high recurrence rate and poor prognosis, posing significant challenges for clinical treatment. Currently, gross total resection (GTR) is the best approach to reduce recurrence and improve prognosis in these patients. However, detailed descriptions of intraoperative findings, particularly for intraspinal cervical CCM, are scarce in the literature. Here, we report a rare case in which the upper cervical spinal CCM mimicked a schwannoma, detailing the surgical treatment strategy and prognosis. Additionally, we analyzed all previously reported cases of spinal CCM to investigate the clinical characteristics, optimal treatment strategies, and prognostic factors, which may be of particular interest to neurosurgeons.

Frontiers in OncologyVol. 14
Sichuan University (CN), West China Hospital of Sichuan University (CN), C.K. Tedam University of Technology and Applied Sciences (GH)
No poverty
Openalex Percentile: Top 25%
Neurofibromatosis and Schwannoma Cases
1.39
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