Belge G, Roque L, Thode B, Fonseca E, Soares J, Clode A, Bartnitzke S, Castedo S, Bullerdiek J
Zentrum für Humangenetik und Genetische Beratung, Universität Bremen.
Verh Dtsch Ges Pathol. 1997;81:151-6.
In order to elucidate cytogenetic changes associated with the development of benign growth of follicular epithelial cells of the thyroid, cytogenetic analyses were performed on 340 follicular thyroid adenomas and goiters after short-term culture. Clonal chromosome changes were found in 67 cases. Trisomy 7 as the sole abnormality or along with other trisomies was the most frequent type of aberration (19 cases). Other recurrent numerical changes were loss of chromosome 22 (4 cases) and the second X or the Y chromosome (5 cases). Translocations involving 19q13 (12 cases) were frequent structural chromosome changes. After a histopathological classification of all cases, we have correlated the cytogenetic findings with the histology of the tumors. Only 8.4% of the goiters showed clonal abnormalities whereas 44.9% of the adenomas revealed clonal abnormalities. Furthermore, simple clonal changes were predominantly found in goiters and complex changes in adenomas. The most impressive correlation was found in the group of lesions with trisomy 7: Whereas all but one lesion with one or two additional trisomies were goiters, those having three or more additional trisomies were all adenomas or adenomatous goiters.
为了阐明与甲状腺滤泡上皮细胞良性生长发育相关的细胞遗传学变化,对340例短期培养后的甲状腺滤泡性腺瘤和甲状腺肿进行了细胞遗传学分析。在67例中发现了克隆性染色体变化。三体性7作为唯一异常或与其他三体性一起是最常见的畸变类型(19例)。其他反复出现的数量变化是22号染色体缺失(4例)以及第二条X或Y染色体缺失(5例)。涉及19q13的易位(12例)是常见的结构性染色体变化。在对所有病例进行组织病理学分类后,我们将细胞遗传学结果与肿瘤组织学进行了关联。只有8.4%的甲状腺肿显示出克隆性异常,而44.9%的腺瘤显示出克隆性异常。此外,单纯的克隆性变化主要见于甲状腺肿,而复杂变化见于腺瘤。在三体性7的病变组中发现了最显著的相关性:除1例有1个或2个额外三体性的病变外,其余所有病变均为甲状腺肿,而有3个或更多额外三体性的病变均为腺瘤或腺瘤性甲状腺肿。