Berg L A, Robert Young S, Brooks K A, Davis A M, Terry Smith S
Department of Obstetrics and Gynecology, University of South Carolina School of Medicine, Columbia, South Carolina.
J Genet Couns. 1996 Mar;5(1):27-38. doi: 10.1007/BF01408663.
In order to determine the incidence of familial and hereditary ovarian cancer in a referral patient population, we conducted a retrospective study of 44 patients from a consecutive set of 62 patients treated for ovarian carcinoma at the Gynecologic Oncology Clinic at the Richland Memorial Hospital Center for Cancer Treatment and Research between January 1, 1993 and December 31, 1993. In our study of the referred patients, only two (4.55%) reported a history of at least one first-degree relative also being affected with ovarian cancer. However, 13 patients (29.55%) reported a family history consistent with one of the hereditary ovarian cancer syndromes. In addition to having a suggestive family history, these 13 families demonstrated several cardinal features of hereditary cancer syndromes including early onset, bilaterality, multiple primary tumors, and transmission. Race was the only significantly different demographic factor between the hereditary and sporadic ovarian cancer groups. All 13 patients who appeared to have a hereditary form of cancer were Caucasian.
为了确定转诊患者群体中家族性和遗传性卵巢癌的发病率,我们对1993年1月1日至1993年12月31日期间在里奇兰纪念医院癌症治疗与研究中心妇科肿瘤诊所接受卵巢癌治疗的连续62例患者中的44例进行了回顾性研究。在我们对转诊患者的研究中,只有2例(4.55%)报告至少有一位一级亲属也患有卵巢癌。然而,13例患者(29.55%)报告的家族史符合遗传性卵巢癌综合征之一。除了有提示性的家族史外,这13个家族还表现出遗传性癌症综合征的几个主要特征,包括发病早、双侧性、多原发性肿瘤和遗传。种族是遗传性和散发性卵巢癌组之间唯一有显著差异的人口统计学因素。所有13例似乎患有遗传性癌症的患者均为白种人。