Pathological Fracture in the Metatarsal Bone Due to an Intraosseous Schwannoma: A Case Report

Intraosseous schwannomas (IOSs) are uncommon benign tumors arising from nerve sheath cells. Schwannomas occurring in the metatarsal bones are extremely uncommon. This case report describes a young adult with a progressively enlarging mass in the foot, which led to limited mobility and ultimately resulted in a pathological fracture of the first metatarsal bone. Imaging studies revealed a diffuse, lytic lesion accompanied by surrounding soft tissue swelling. Histopathological evaluation confirmed the diagnosis of a schwannoma. Notably, this case highlights a key diagnostic challenge: its radiological and immunohistochemical features can be ambiguous. Although findings such as an elevated Ki-67 index suggested potential low-grade malignant transformation, retained H3K27me3 expression and an indolent clinical course confirmed the benign nature of the lesion. This case underscores the diagnostic complexity of ambiguous skeletal lesions and emphasizes the necessity of integrating clinical, radiological, and pathological assessments to achieve an accurate diagnosis and guide management. Reporting this case in the literature should help enhance awareness of rare variants of IOSs and advocate for the adoption of an integrated clinical-radiological-pathological workflow when managing ambiguous skeletal lesions.

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Publication Details

Journal
Cureus
Published
2025-10-22
DOI
https://doi.org/10.7759/cureus.95134
Primary Topic
Neurofibromatosis and Schwannoma Cases
Type
article
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article

Pathological Fracture in the Metatarsal Bone Due to an Intraosseous Schwannoma: A Case Report

Desheng Song, Zhaoshu Huang, Lingling Song, Luming Shen et al.
Cureus
Neurofibromatosis and Schwannoma Cases
article

Pathological Fracture in the Metatarsal Bone Due to an Intraosseous Schwannoma: A Case Report

Desheng Song, Zhaoshu Huang, Lingling Song, Luming Shen, Yining Xiang
article en

Abstract

Intraosseous schwannomas (IOSs) are uncommon benign tumors arising from nerve sheath cells. Schwannomas occurring in the metatarsal bones are extremely uncommon. This case report describes a young adult with a progressively enlarging mass in the foot, which led to limited mobility and ultimately resulted in a pathological fracture of the first metatarsal bone. Imaging studies revealed a diffuse, lytic lesion accompanied by surrounding soft tissue swelling. Histopathological evaluation confirmed the diagnosis of a schwannoma. Notably, this case highlights a key diagnostic challenge: its radiological and immunohistochemical features can be ambiguous. Although findings such as an elevated Ki-67 index suggested potential low-grade malignant transformation, retained H3K27me3 expression and an indolent clinical course confirmed the benign nature of the lesion. This case underscores the diagnostic complexity of ambiguous skeletal lesions and emphasizes the necessity of integrating clinical, radiological, and pathological assessments to achieve an accurate diagnosis and guide management. Reporting this case in the literature should help enhance awareness of rare variants of IOSs and advocate for the adoption of an integrated clinical-radiological-pathological workflow when managing ambiguous skeletal lesions.

CureusVol. 17(10)
Affiliated Hospital of Guizhou Medical University (CN)
Openalex Percentile: Top 57%
Neurofibromatosis and Schwannoma Cases
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