Sacrococcygeal chordomas: problems in diagnosis and management.

Abstract:

:Chordomas are rare, insidious, and slow-growing but locally aggressive, malignant tumors originating from the primitive notochord and localized along the axial skeleton. Between 1988 and 1993, four patients with sacrococcygeal chordomas were treated at the Ankara Numune State Hospital. There was a median 17-month interval between the onset of symptoms and diagnosis. In all patients, a posterior approach was used. In addition, two patients were treated with adjuvant radiation therapy. There were no serious intra- or postoperative complications. Early diagnosis and surgery plus radiation therapy seem to provide the best results in terms of survival.

authors

Turgut M,Gül B,Taşkin Y

doi

10.1007/BF00703453

subject

Has Abstract

pub_date

1998-01-01 00:00:00

pages

100-2

issue

1-2

eissn

0936-8051

issn

1434-3916

journal_volume

117

pub_type

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