Hasle H, Olsen J H, Nielsen J, Hansen J, Friedrich U, Tommerup N
Department of Paediatrics, Odense University Hospital, Denmark.
Br J Cancer. 1996 May;73(9):1156-9. doi: 10.1038/bjc.1996.222.
A study of cancer incidence in a cohort of 597 women with Turner syndrome (TS) and a virtually complete follow-up is presented. The cohort was established from the Danish Cytogenetic Register. Information on cancer incidence was obtained from the Danish Cancer Registry and compared with the expected number calculated from the age-, period- and site-specific cancer rates for Danish women. A total of 21 neoplasms was observed, of which 13 occurred more than 1 year after diagnosis of TS, corresponding to a relative risk of cancer of 1.1. Wilms' tumour was the only identified childhood cancer. No case of gonadoblastoma or dysgerminoma was identified in the 29 women with a Y chromosome or in the women in whom no Y chromosome material was detected by standard cytogenetic methods, suggesting that the risk of ovarian germ cell tumours may be lower than previously estimated. Colon cancer was observed in five patients (relative risk 6.9, 95% confidence interval 2.2-16.2). Further studies are needed to assess whether colon cancer in TS is related to Turner-associated genes on the sex chromosome(s).
本文呈现了一项针对597名特纳综合征(TS)女性队列的癌症发病率研究,且随访几乎完整。该队列由丹麦细胞遗传学登记处建立。癌症发病率信息取自丹麦癌症登记处,并与根据丹麦女性的年龄、时期和部位特异性癌症发病率计算出的预期数量进行比较。共观察到21例肿瘤,其中13例在TS诊断后1年以上发生,对应的癌症相对风险为1.1。肾母细胞瘤是唯一确诊的儿童期癌症。在29名有Y染色体的女性或通过标准细胞遗传学方法未检测到Y染色体物质的女性中,未发现一例性腺母细胞瘤或无性细胞瘤,这表明卵巢生殖细胞肿瘤的风险可能低于先前估计。5名患者观察到结肠癌(相对风险6.9, 95%置信区间2.2 - 16.2)。需要进一步研究以评估TS中的结肠癌是否与性染色体上的特纳相关基因有关。