Belge G, Thode B, Bartnitzke S, Bullerdiek J
Center of Human Genetics and Genetic Counselling, University of Bremen, Germany.
Cancer Genet Cytogenet. 1994 Nov;78(1):102-4. doi: 10.1016/0165-4608(94)90055-8.
Cytogenetic aberrations have been described in about 30% of benign thyroid tumors, but their role for tumorigenesis or progression has not yet been elucidated. We describe the cytogenetic analyses in a thyroid adenoma with two different clonal cytogenetic stemlines: 45,XX,der(1)t(1;14)(p13;q11.2-q(13),t(5;12)(q11.2;q24),del(9)(q12),- 10,der(11)t(11;?;19)(p15;q13),der(14)t(14;15)(q11.2-q13;q23),del(15)(q23 ), der(15)t(9;15)(q12;p10),der(19)t(10;19)(q11.2;q13)/46,X,?inv(x),?inv(3) (p21q29),t(3;8)(q26;q12). Histologic examination revealed an atypical follicular thyroid adenoma containing microfollicular, follicular, trabecular-solid, and oncocytic components. There may be a direct relation between the different cytogenetic stemlines and the histologic diversity of the tumor. Thyroid tumors with complex karyotypes involving the 19q13 breakpoint may represent advanced stages of karyotypic evolution and therefore warrant an extensive clinical follow-up.
约30%的良性甲状腺肿瘤中已发现细胞遗传学异常,但其在肿瘤发生或进展中的作用尚未阐明。我们描述了对一例甲状腺腺瘤的细胞遗传学分析,该腺瘤具有两种不同的克隆细胞遗传学主干系:45,XX,der(1)t(1;14)(p13;q11.2-q(13),t(5;12)(q11.2;q24),del(9)(q12),- 10,der(11)t(11;?;19)(p15;q13),der(14)t(14;15)(q11.2-q13;q23),del(15)(q23 ), der(15)t(9;15)(q12;p10),der(19)t(10;19)(q11.2;q13)/46,X,?inv(x),?inv(3) (p21q29),t(3;8)(q26;q12)。组织学检查显示为非典型滤泡性甲状腺腺瘤,含有微滤泡、滤泡、小梁-实性和嗜酸性细胞成分。不同的细胞遗传学主干系与肿瘤的组织学多样性之间可能存在直接关系。涉及19q13断点的复杂核型的甲状腺肿瘤可能代表核型进化的晚期阶段,因此需要进行广泛的临床随访。