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Asian Spine Journal ; : 353-356, 2014.
Article Dans Anglais | WPRIM | ID: wpr-91704

Résumé

Thoracic chordomas are very rare malignant tumours originating from notochordal remnants. These tumours develop within a vertebral body and enlarge involving the mediastinal compartment. Because of their slow-growing attitude, they become symptomatic only when they invade or compress the spinal cord and/or mediastinal organs. We present a rare case of a thoracic spine chordoma presenting with increasing paraparesis with a huge mediastinal component which was surgically debulked to decompress the spinal cord and medistinal organs.


Sujets)
Tumeurs osseuses , Chordome , Médiastin , Chorde , Paraparésie , Moelle spinale , Rachis
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