Chordoma: incidence and survival patterns in the United States, 1973–1995

被引：0
作者：
Mary L. McMaster
Alisa M. Goldstein
Christina M. Bromley
Naoko Ishibe
Dilys M. Parry
机构：
[1] National Cancer Institute,Genetic Epidemiology Branch, Division of Cancer Epidemiology and Genetics
[2] National Institutes of Health,undefined
来源：
Cancer Causes & Control | 2001年 / 12卷
关键词：
bone neoplasms; chordoma; epidemiology; SEER;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
Background: Chordoma, a rare tumor arising from notochordal remnants, has been described to date only by single-institution case series or small population-based surveys.
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页码：1 / 11
页数：10
相关论文
共 176 条
[1]  
Salisbury JR(1993)The pathology of the human notochord J Pathol 171 253-255
[2]  
Ho KL(1985)Ecchordosis physaliphora and chordoma: a comparative ultrastructural study Clin Neuropathol 4 77-86
[3]  
Paavolainen P(1976)Chordoma in Finland Acta Orthop Scand 47 46-51
[4]  
Teppo L(1981)Chordoma. A clinicopathologic and prognostic study of a Swedish national series Acta Orthop Scand 52 49-58
[5]  
Eriksson B(1985)Fifty years of experience with chordomas in southeast Scotland Neurosurgery 16 166-170
[6]  
Gunterberg B(1977)Incidence of bone sarcoma in SW England, 1946-74, in relation to age, sex, tumour site and histology Br J Cancer 36 511-522
[7]  
Kindblom LG(1990)Primary tumors of the axial skeleton. Experience of the Leeds Regional Bone Tumor Registry Spine 15 137-140
[8]  
O'Neill P(1995)Bone cancers Cancer 75 203-210
[9]  
Bell BA(1973)Chordomas and cartilaginous tumors at the skull base Cancer 32 410-420
[10]  
Miller JD(1964)An evaluation of the diagnosis and treatment of chordoma J Neurol Neurosurg Psychiatry 27 157-165
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