1.
Przegl Lek
; 56(2): 115-8, 1999.
Artigo
em Polonês
| MEDLINE
| ID: mdl-10375941
RESUMO
Chordoma is a relatively rare neoplasm originating from the remnants of the embryonic notochord. We analysed 24 cases of chordoma. The patients were divided into groups depending on the localisation. We analysed the results of different methods of therapy: surgical treatment, radiation therapy and combined surgical and radiological treatment. The results were compared with the data from the references.