Chordoma: retrospective analysis of 24 cases

Author:

Lopes Ademar1,Rossi Benedito Mauro1,Silveira Claudio Regis Sampaio1,Alves Antonio Correa1

Affiliation:

1. A. C. Camargo Hospital, Brazil

Abstract

INTRODUCTION: Chordoma is a rare and slow-growing tumor, with local aggressiveness and preferential localization in the vertebral column. OBJECTIVE: The main objective of this study is to evaluate natural history and results of treatment of chordomas. METHODOLOGY: This is a retrospective study from 1953 to 1993. MATERIAL AND METHODS: The age ranged from 2 to 86 years (mean=34.5). Twelve patients were male and 12 female. The localization of the tumor was: 20 in the sacral region, 3 in head and neck and one out of the spine. RESULTS: The treatment, alone or combined, was surgery, radiation therapy and chemotherapy. The survival rate for patients with lesions in the sacrum ranged from 4 to 119 months, since the date of the symptoms. The 5-year overall survival was 4.2%. CONCLUSION: Chordoma is a rare and slow growing tumor, with a very difficult approach by surgery due to its preferential location in the sacrum and poor therapeutic results with radiation therapy or chemotherapy, mainly in patients with advanced disease.

Publisher

FapUNIFESP (SciELO)

Subject

General Medicine

Reference19 articles.

Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. OFTALMOPLEGIA INTERNUCLEAR COM PARALISIA DE RETO LATERAL ESQUERDO COM TUMOR DE CLIVUS;Revista Contemporânea;2024-01-29

2. Surgical management of chordoma: A systematic review;The Journal of Spinal Cord Medicine;2018-07-26

3. SACROCOCCYGEAL CHORDOMA DIAGNOSED BY FNAC: A RARE CASE REPORT;Journal of Evolution of Medical and Dental Sciences;2014-05-31

4. Natural history and surgical treatment of chordoma: a retrospective cohort study;Sao Paulo Medical Journal;2014

5. Pediatric Tumors Involving the Spinal Column;Neurosurgery Clinics of North America;2008-01

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