Fletcher J A, Gibas Z, Donovan K, Perez-Atayde A, Genest D, Morton C C, Lage J M
Department of Pathology, Brigham and Women's Hospital MA 02115.
Am J Pathol. 1991 Mar;138(3):515-20.
Eleven ovarian granulosa-stromal cell tumors including 1 thecoma, 2 fibromas, 6 fibrothecomas, and 2 granulosa cell tumors, were karyotyped after direct harvest and/or short-term tissue culture. Bilateral fibrothecomas from one patient appeared to lack cytogenetic aberrations: the remaining nine tumors were characterized by trisomy for chromosome 12. Cytogenetic aberrations in the two granulosa cell tumors were much less complex than those described previously in undifferentiated carcinomas; accordingly cytogenetic analyses might be useful in distinguishing these categories. The consistent occurrence of trisomy 12 in different varieties of granulosa-stromal cell tumors suggests a common mechanism of oncogenesis within this diverse group of neoplasms. That mechanism probably involves promotion of low-grade, orderly cell proliferation.
对11例卵巢颗粒-间质细胞瘤进行了核型分析,其中包括1例卵泡膜瘤、2例纤维瘤、6例纤维卵泡膜瘤和2例颗粒细胞瘤,样本均直接采集和/或经短期组织培养获得。1例患者的双侧纤维卵泡膜瘤似乎没有细胞遗传学异常:其余9例肿瘤的特征是12号染色体三体。这2例颗粒细胞瘤的细胞遗传学异常远没有之前在未分化癌中描述的那么复杂;因此,细胞遗传学分析可能有助于区分这些类型。不同类型的颗粒-间质细胞瘤中均一致出现12号染色体三体,这表明在这一多样的肿瘤群体中存在共同的肿瘤发生机制。该机制可能涉及促进低度、有序的细胞增殖。