- Author:
Ottavio RENA
1
;
Fabio DAVOLI
;
Giuliano ALLEGRA
;
Caterina CASADIO
;
Davide TURELLO
Author Information
- Publication Type:Case Report
- Keywords: Chordoma; Spine; Bone neoplasms; Mediastinum; Surgery
- MeSH: Bone Neoplasms; Chordoma*; Mediastinum; Notochord; Paraparesis; Spinal Cord; Spine*
- From:Asian Spine Journal 2014;8(3):353-356
- CountryRepublic of Korea
- Language:English
- 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.