Mäkitie O, Pukkala E, Teppo L, Kaitila I
Hospital for Children and Adolescents and the Department of Clinical Genetics, Helsinki University Hospital, Finland.
J Pediatr. 1999 Mar;134(3):315-8. doi: 10.1016/s0022-3476(99)70456-7.
Previous reports have suggested an increased risk of cancer among patients with cartilage-hair hypoplasia (CHH). This study was carried out to further evaluate this risk among patients with CHH and their first-degree relatives.
One hundred twenty-two patients with CHH were identified through 2 countrywide epidemiologic surveys in 1974 and in 1986. Their parents and nonaffected siblings were identified through the Population Register Center. This cohort underwent follow-up for cancer incidence through the Finnish Cancer Registry to the end of 1995.
A statistically significant excess risk of cancer was seen among the patients with CHH (standardized incidence ratio 6.9, 95% confidence interval 2.3 to 16), which was mainly attributable to non-Hodgkin's lymphoma (standardized incidence ratio 90, 95% confidence interval 18 to 264). In addition, a significant excess risk of basal cell carcinoma was seen (standardized incidence ratio 35, 95% confidence interval 7.2 to 102). The cancer incidence among the siblings or the parents did not differ from the average cancer incidence in the Finnish population.
This study confirms an increased risk of cancer, especially non-Hodgkin's lymphoma, probably attributable to defective immunity, among patients with CHH.
既往报告提示软骨毛发发育不全(CHH)患者患癌风险增加。本研究旨在进一步评估CHH患者及其一级亲属的患癌风险。
通过1974年和1986年两次全国性流行病学调查确定了122例CHH患者。通过人口登记中心确定了他们的父母和未患病的兄弟姐妹。该队列通过芬兰癌症登记处对癌症发病率进行随访至1995年底。
CHH患者中观察到具有统计学意义的癌症超额风险(标准化发病比6.9,95%置信区间2.3至16),这主要归因于非霍奇金淋巴瘤(标准化发病比90,95%置信区间18至264)。此外,还观察到基底细胞癌有显著的超额风险(标准化发病比35,95%置信区间7.2至102)。兄弟姐妹或父母的癌症发病率与芬兰人群的平均癌症发病率无差异。
本研究证实CHH患者患癌风险增加,尤其是非霍奇金淋巴瘤,可能归因于免疫缺陷。