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A Rare Case of an Osteoid Osteoma of the Cervical Spine
Author(s) -
Silva Gomes Francisco,
Alves Cristina,
Cardoso Pedro Sa,
Ling Tah Pu
Publication year - 2020
Publication title -
case reports in orthopedic research
Language(s) - English
Resource type - Journals
ISSN - 2296-9373
DOI - 10.1159/000508371
Subject(s) - case report
Osteoid osteoma (OO) is a benign bone tumor rarely affecting the cervical spine. OO, currently diagnosed by X-ray, computed tomography (CT), bone scan, and magnetic resonance imaging, is difficult to identify when located in the cervical spine based on spine radiographs due to their usually small size and the complex anatomy of the cervical spine. CT scans successfully diagnose 20–30% of the small osteolytic lesions with dense sclerotic rings and central calcifications and the anatomic location of the nidus. CT-guided radiofrequency ablation is a noninvasive treatment option widely used. However, in specific cases, surgical resection of the nidus is recommended. We present a rare clinical case of cervical spine OO of a 16-year-old female patient. The lesion was located on the left lamina of C7, and once the diagnosis was established by physical examination and imaging, laminectomy and cervical arthrodesis (C6-T1) were performed. Twelve months after the surgical intervention, the patient showed complete remission of the symptoms and no disabilities.

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