| Literature DB >> 1602449 |
D Winants1, A Bertal, L Hennequin, J Fays, P Bernadac.
Abstract
Chordoma is a rare tumor in spine. Two cases, exceptional in adolescents, are reported. The clinical evolution is slow and progressive. CT shows a lobulated tumor, precises the degree of vertebral osteolysis and detects intra-tumoral calcifications. MRI is useful to determine especially in high in soft tissues and the vertebral canal. Arteriography is realised in pre-operative time and permits an embolization when the tumor is hypervascularised.Entities:
Mesh:
Year: 1992 PMID: 1602449
Source DB: PubMed Journal: J Radiol ISSN: 0221-0363