Berger R, Bernheim A, Tsapis A, Brouet J C, Seligmann M
Cancer Genet Cytogenet. 1986 Jul;22(3):219-23. doi: 10.1016/0165-4608(86)90158-5.
Cytogenetic studies were performed in four cases of alpha chain disease. Chromosomal abnormalities were found in the lymphoid cells of the mesenteric lymph nodes of three patients, two of whom had not reached the stage of overt malignant lymphoma. In two instances, a rearrangement of 14q32, resulting from a t(9;14)(p11;q32) and a t(2;14)(p12;q32) was observed. One case showed complex rearrangements including t(5;9). No abnormalities were found in the intestinal tumor of the fourth case with immunoblastic lymphoma. It is concluded that alpha chain disease is a clonal proliferation with frequent alteration of chromosome #14 at band q32 resulting from translocations that differ from those observed in the vast majority of other non-Hodgkin lymphomas.
对4例α链病患者进行了细胞遗传学研究。在3例患者的肠系膜淋巴结淋巴细胞中发现了染色体异常,其中2例尚未达到明显恶性淋巴瘤阶段。在2例中,观察到由t(9;14)(p11;q32)和t(2;14)(p12;q32)导致的14q32重排。1例显示包括t(5;9)在内的复杂重排。第4例免疫母细胞淋巴瘤患者的肠道肿瘤未发现异常。结论是,α链病是一种克隆性增殖,其14号染色体q32带频繁发生改变,这是由与绝大多数其他非霍奇金淋巴瘤中观察到的不同的易位所致。