Abstract
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.
Lingua originale | Inglese |
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pagine (da-a) | 353-356 |
Numero di pagine | 4 |
Rivista | Asian Spine Journal |
Volume | 8 |
Numero di pubblicazione | 3 |
DOI | |
Stato di pubblicazione | Pubblicato - 2014 |