Case Report: Intraosseous schwannoma of the thoracic spine: two case reports and an updated review of the literature

Intraosseous schwannomas (IOSs) are benign tumors composed of nerve sheath cells, representing less than 0.2% of primary bone tumors. These tumors most commonly affect the mandible and sacrum, while vertebral involvement remains exceedingly rare. Herein, we present two cases of SISs located at the T2 and T8 vertebrae. We detail the clinical presentation, imaging features, histopathological characteristics, and surgical management of SISs to advance the understanding of this rare condition. Typically presenting as expansile lytic lesions with sclerotic margins, lacking periosteal reaction or calcification, SISs frequently cause foraminal widening and vertebral scalloping, which are characteristic imaging findings that differentiate them from other bone tumors. Complete tumor resection is the recommended treatment, and spinal fusion is often necessary for reconstruction, with recurrence being uncommon after surgery. Additionally, we conduct a review of the existing literature and engage in a discussion regarding this uncommon tumor, enriching clinicians' differential diagnosis of vertebral body osteolytic lesions and providing valuable clinical experience for the individualized selection of surgical approaches.

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Publication Details

Journal
Frontiers in Oncology
Published
2025-10-22
DOI
https://doi.org/10.3389/fonc.2025.1651417
Primary Topic
Neurofibromatosis and Schwannoma Cases
Type
article
Field-Weighted Citation Impact
0.00

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article

Case Report: Intraosseous schwannoma of the thoracic spine: two case reports and an updated review of the literature

Hangqi Hu, Dan Cao, Xiping Yu, Xian Wang et al.
Frontiers in Oncology
Neurofibromatosis and Schwannoma Cases
article

Case Report: Intraosseous schwannoma of the thoracic spine: two case reports and an updated review of the literature

Hangqi Hu, Dan Cao, Xiping Yu, Xian Wang, Houyun Xu, Jibo Hu
article en

Abstract

Intraosseous schwannomas (IOSs) are benign tumors composed of nerve sheath cells, representing less than 0.2% of primary bone tumors. These tumors most commonly affect the mandible and sacrum, while vertebral involvement remains exceedingly rare. Herein, we present two cases of SISs located at the T2 and T8 vertebrae. We detail the clinical presentation, imaging features, histopathological characteristics, and surgical management of SISs to advance the understanding of this rare condition. Typically presenting as expansile lytic lesions with sclerotic margins, lacking periosteal reaction or calcification, SISs frequently cause foraminal widening and vertebral scalloping, which are characteristic imaging findings that differentiate them from other bone tumors. Complete tumor resection is the recommended treatment, and spinal fusion is often necessary for reconstruction, with recurrence being uncommon after surgery. Additionally, we conduct a review of the existing literature and engage in a discussion regarding this uncommon tumor, enriching clinicians' differential diagnosis of vertebral body osteolytic lesions and providing valuable clinical experience for the individualized selection of surgical approaches.

Frontiers in OncologyVol. 15
Sir Run Run Shaw Hospital (CN), The Fourth People's Hospital (CN), Zhejiang University (CN)
Jinhua Science and Technology Bureau
Openalex Percentile: Top 57%
Neurofibromatosis and Schwannoma Cases
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