Teixeira M R, Qvist H, Giercksky K E, Bøhler P J, Heim S
Department of Genetics, Norwegian Radium Hospital, Oslo, Norway.
Cancer Genet Cytogenet. 1997 Feb;93(2):157-9. doi: 10.1016/s0165-4608(96)00186-0.
Epithelial proliferative lesions of the appendix are rare and have never been studied cytogenetically. We present the chromosomal banding analysis of four successfully short-term cultured samples from pseudomyxoma peritonei lesions originating from a cystadenoma of the appendix. All four sample contained clonal chromosome abnormalities. In three of them, the clone 46,XX,der(6)?del(6)(q16q21)?del(6)(q27) was found, whereas a clone with the karyotype 46,XX,t(2;17)(p21;p13),t(6;12)(p21;q13),t(12;15)(q24;q15) was detected in the fourth sample. Our findings support the view that pseudomyxoma peritonei originates by spreading from a primary mucinous neoplasm of an intraperitoneal organ rather than through mucinous metaplasia or multifocal primary neoplastic transformation of the peritoneum.
阑尾上皮增生性病变罕见,且从未进行过细胞遗传学研究。我们对4例源自阑尾囊腺瘤的腹膜假黏液瘤病变成功进行短期培养的样本进行了染色体显带分析。所有4个样本均含有克隆性染色体异常。其中3个样本中发现了克隆46,XX,der(6)?del(6)(q16q21)?del(6)(q27),而在第4个样本中检测到了核型为46,XX,t(2;17)(p21;p13),t(6;12)(p21;q13),t(12;15)(q24;q15)的克隆。我们的研究结果支持以下观点,即腹膜假黏液瘤起源于腹膜内器官的原发性黏液性肿瘤的播散,而非通过黏液化生或腹膜的多灶性原发性肿瘤转化。