Cervical Myelopathy Due to an Osteochondroma in Multiple Hereditary Exostosis

Hereditary multiple exostosis is a rare genetic condition characterized by the development of multiple exostoses. Vertebral localization is rare, less than 7%. Spinal cord compression in hereditary multiple exostosis is a rare condition. We report the case of a 22‐year‐old man with cervical spinal cord compression due to an osteochondroma with neurological impairment. A decompressive laminectomy was performed, resulting in complete resection of the exostosis. The postoperative course was characterized by the complete resolution of neurological symptoms.

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Publication Details

Journal
Case Reports in Orthopedics
Published
2026-01-01
DOI
https://doi.org/10.1155/cro/5557776
Primary Topic
Bone Tumor Diagnosis and Treatments
Type
article
Field-Weighted Citation Impact
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article

Cervical Myelopathy Due to an Osteochondroma in Multiple Hereditary Exostosis

Xavier Banse, Pierre-Louis Docquier, Cédric Dongmo Mayopa, Géraud Garcia Segbedji
Case Reports in Orthopedics
Bone Tumor Diagnosis and Treatments
article

Cervical Myelopathy Due to an Osteochondroma in Multiple Hereditary Exostosis

Xavier Banse, Pierre-Louis Docquier, Cédric Dongmo Mayopa, Géraud Garcia Segbedji
article en

Abstract

Hereditary multiple exostosis is a rare genetic condition characterized by the development of multiple exostoses. Vertebral localization is rare, less than 7%. Spinal cord compression in hereditary multiple exostosis is a rare condition. We report the case of a 22‐year‐old man with cervical spinal cord compression due to an osteochondroma with neurological impairment. A decompressive laminectomy was performed, resulting in complete resection of the exostosis. The postoperative course was characterized by the complete resolution of neurological symptoms.

Case Reports in OrthopedicsVol. 2026(1)
Cliniques Universitaires Saint-Luc (BE), Neuroelectronics Research Flanders (BE)
Good health and well-being
Openalex Percentile: Top 6%
Bone Tumor Diagnosis and Treatments
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