Abstract
Chordomas are rare tumours arising from embryonic notochord tissue remnants. The commonest affected segment is the sacrum. This localization may present diagnostic and therapeutic problems. Two cases of chordoma treated by surgery and radiation are reported.
Publication types
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Case Reports
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English Abstract
MeSH terms
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Aged
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Chordoma / diagnosis
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Chordoma / radiotherapy
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Chordoma / surgery
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Chordoma / therapy*
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Coccyx*
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Combined Modality Therapy
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Diagnosis, Differential
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Female
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Humans
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Male
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Middle Aged
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Radiotherapy Dosage
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Sacrum*
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Spinal Neoplasms / diagnosis
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Spinal Neoplasms / radiotherapy
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Spinal Neoplasms / surgery
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Spinal Neoplasms / therapy*