Belge G, Thode B, Rippe V, Bartnitzke S, Bullerdiek J
Zentrum für Humangenetik und genetische Beratung, Universität Bremen, Germany.
Hum Genet. 1994 Aug;94(2):198-202. doi: 10.1007/BF00202871.
The cytogenetic results from a series of 113 thyroid hyperplasias and adenomas are reported; 15 showed clonal karyotypic alterations. In addition to a group showing translocations involving 19q13, another subset of lesions characterized by polysomies can be found. Based on our own cases belonging to this subset and a review of the cases reported in the literature, we conclude that the characteristic feature of this group is a sequence that always starts with trisomy 7, but that sometimes even leads to chromosome numbers in the hypertriploid range. This subset of thyroid tumors may be an example of a more common genetic pathway in human solid tumors.
报告了113例甲状腺增生和腺瘤的细胞遗传学结果;15例显示克隆性核型改变。除了一组显示涉及19q13的易位外,还可发现另一组以多倍体为特征的病变。基于我们自己属于该亚组的病例以及对文献报道病例的回顾,我们得出结论,该组的特征是一个总是从7号染色体三体开始的序列,但有时甚至会导致超三倍体范围内的染色体数目。甲状腺肿瘤的这一亚组可能是人类实体瘤中更常见遗传途径的一个例子。