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Surgical neurology international · 2026

Cervical spinal myelopathy secondary to cervical exostoses: A rare cause of cord compression - A case report.

Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Palescandolo Dario, Ali Sohaib, Melatini Alessandro, Rolli Marilena, Cassitto Domenico, Giaquinta Alessandra, Mastromatteo Francesco, Esposito Manfredo, Nizzola Mariagrazia, Ali Kumail, Sadia Haleema, Voena Vittorio, Ruggieri Antonio, Cosimo Damiano Gianfreda

Аннотация

BACKGROUND: Multiple hereditary exostoses (MHE) is a rare autosomal dominant disorder. It is characterized by the development of cartilage-capped bony outgrowths arising from the epiphyseal or diaphyseal regions of long bones, leading to reduced joint motion and pain secondary to compression. MHE is attributed to the predominant exostin-1 and exostin-2 mutations that cause multiple osteochondromas. The most common locations of these lesions are on the knee joint, humerus, pelvis, scapula, and also the spine.

CASE DESCRIPTION: A 26-year-old Caucasian male with a diagnosis of MHE, presenting with progressive spastic tetraparesis. The cervical magnetic resonance (MR) revealed an osteochondroma arising from the C2 lamina dorsolaterally compressing the spinal cord at the C1-C2 level. Following a C2 laminectomy, the postoperative MR imaging confirmed gross total lesion excision. Postoperatively, the patient's myelopathy gradually improved and was discharged to a rehabilitation facility.

CONCLUSION: Rarely, MHE spinal osteochondromas cause spinal cord compression that is readily relieved with typical decompressive procedures.

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

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