Kerzin-Storrar L, Faed M J, MacGillivray J B, Smith P G
Br J Cancer. 1983 May;47(5):707-12. doi: 10.1038/bjc.1983.109.
The family histories of 131 patients with histologically defined Hodgkin's disease (HD) were studied and 2,517 first and second degree relatives and spouses were identified and followed-up. The causes of death in deceased relatives were ascertained from death certificates. The numbers of deaths from selected causes were compared with the numbers that would be expected if the relatives had suffered the same mortality rates as the Scottish national population. A 4-fold increase in deaths due to HD was found among first and second degree relatives of patients with the disease (6 cases observed compared with 1.4 expected). Five of the 6 familial cases were related to index patients with the mixed cellularity form of the disease, the remaining case was the brother of a patient with the lymphocyte-depleted form of the disease. The increased risk was seen among relatives of both young and older patients and there was no consistent intrafamilial similarity in age of onset or time of onset of disease.
对131例经组织学确诊的霍奇金淋巴瘤(HD)患者的家族史进行了研究,确定并随访了2517名一级和二级亲属及配偶。从死亡证明中查明已故亲属的死因。将特定原因导致的死亡人数与亲属若与苏格兰全国人口死亡率相同情况下预期的死亡人数进行比较。在该病患者的一级和二级亲属中,发现因HD导致的死亡人数增加了4倍(观察到6例,预期为1.4例)。6例家族性病例中有5例与患有混合细胞型疾病的索引患者有关,其余1例是患有淋巴细胞消减型疾病患者的兄弟。在年轻和老年患者的亲属中均观察到风险增加,且发病年龄或发病时间在家族内部没有一致的相似性。