Fanconi anemia - Adult head and neck cancer and hematopoietic mosaicism

被引:46
作者
Alter, BP
Joenje, H
Oostra, AB
Pals, G
机构
[1] Natl Canc Inst, Dept Hlth & Human Serv, Div Canc Epidemiol & Genet, Clin Genet Branch, Rockville, MD 20852 USA
[2] Vrije Univ Amsterdam, Med Ctr, Dept Clin Genet & Human Genet, NL-1081 HV Amsterdam, Netherlands
关键词
D O I
10.1001/archotol.131.7.635
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Fanconi anemia (FA) is an autosomal recessive DNA repair disorder with a very high risk of cancer. (1,2)While most of the homozygotes are identified clinically because of characteristic birth defects and early-onset aplastic anemia, (3)a subset of patients, often with milder physical and hematologic phenotypes, remain undiagnosed. They are at very high risk of neoplasms, including acute myeloid leukemias and solid tumors. (4)All types of solid tumors (combined) develop at a rate that is 48 times greater than that experienced by the general population, and the cancer hazard rate is 2% per year by the age of 24 years, with a cumulative incidence in a competing risk model of 29% by the age of 45 years.(5)
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收藏
页码:635 / 639
页数:5
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