Dural contact in a high cervical paraspinal spindle cell neoplasm

Background: Paraspinal spindle cell mesenchymal neoplasms of myofibroblastic origin are extremely rare, particularly in the high cervical region. Radiologic differentiation between dural contact and true invasion is often challenging. Case Description: A 52-year-old female presented with posterior neck pain and a palpable upper cervical mass. The magnetic resonance demonstrated a 6 × 4 cm paraspinal lesion at the C1–C2 level with suspected dural involvement. Surgical exploration revealed a well-encapsulated tumor extending to the dura without true invasion; this allowed for gross total resection with dural preservation. Histopathology confirmed a benign myofibroblastic spindle cell neoplasm with a low Ki-67 index (1%). The patient experienced complete postoperative symptom resolution, and at 13 months postoperatively, had no radiologic evidence of recurrence. Conclusion: Radiologic dural contact should not be assumed to represent true dural invasion. In these benign lesions, intraoperative assessment allows for safe gross total resection with full dural preservation and the avoidance of a cerebrospinal fluid leak.

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Publication Details

Journal
Surgical Neurology International
Published
2026-05-01
DOI
https://doi.org/10.25259/sni_220_2026
Primary Topic
Soft tissue tumor case studies
Type
article
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article

Dural contact in a high cervical paraspinal spindle cell neoplasm

Fazlı Oğuzhan Durak, Mevlüde Güneş
Surgical Neurology International
Soft tissue tumor case studies
article

Dural contact in a high cervical paraspinal spindle cell neoplasm

Fazlı Oğuzhan Durak, Mevlüde Güneş
article en

Abstract

Background: Paraspinal spindle cell mesenchymal neoplasms of myofibroblastic origin are extremely rare, particularly in the high cervical region. Radiologic differentiation between dural contact and true invasion is often challenging. Case Description: A 52-year-old female presented with posterior neck pain and a palpable upper cervical mass. The magnetic resonance demonstrated a 6 × 4 cm paraspinal lesion at the C1–C2 level with suspected dural involvement. Surgical exploration revealed a well-encapsulated tumor extending to the dura without true invasion; this allowed for gross total resection with dural preservation. Histopathology confirmed a benign myofibroblastic spindle cell neoplasm with a low Ki-67 index (1%). The patient experienced complete postoperative symptom resolution, and at 13 months postoperatively, had no radiologic evidence of recurrence. Conclusion: Radiologic dural contact should not be assumed to represent true dural invasion. In these benign lesions, intraoperative assessment allows for safe gross total resection with full dural preservation and the avoidance of a cerebrospinal fluid leak.

Surgical Neurology InternationalVol. 17
Gender equality
Openalex Percentile: Top 8%
Soft tissue tumor case studies
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