Related Experiment Video For Multiple hereditary exostosis
Updated: Jul 13, 2026

Calibrated Forceps Model of Spinal Cord Compression Injury
Published on: April 24, 2015
Multiple hereditary osteochondromatosis with spinal cord compression: case report
Oscar García-González1,2, J Nicolás Mireles-Cano3, Natalia Sánchez-Zavala4
1Hospital Regional de Alta especialidad del Bajío, León, Guanajuato, Mexico. oggarciagonzalez@gmail.com.
Objective:
The purpose of the report is to describe a patient with hereditary osteochondromatosis and spinal cord compression at the thoracic level.
Clinical Features:
An 8-year-old patient with hereditary osteochondromatosis inherited from his father presented paraparesis in the left foot, leading to complete paralysis in both legs.
Intervention:
In a CT scan, a bony tumor rising from the posterior wall of the T3 body narrowing the spinal canal, and the MRI spinal cord compression at the same level and the hydrosyringomyelic cavity extended to the conus medullaris; with an anterior thoracic approach to T2-T4, the fibro-cartilaginous tumor was removed, and the stabilization was completed with bone graft and a plate. Two months after surgery, the patient recovered strength in both legs.
Conclusions:
A detailed family history through examination-guided advanced imaging and biopsy provides useful information for diagnosis and appropriate management of occupative lesions in patients affected with multiple hereditary exostosis.
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