Nilbert M, Heim S, Mandahl N, Flodérus U M, Willén H, Mitelman F
Department of Clinical Genetics, University Hospital, Lund, Sweden.
Hum Genet. 1990 Oct;85(6):605-11. doi: 10.1007/BF00193583.
The cytogenetic analysis of 224 leiomyomas from 138 patients is presented. An insufficient number of mitoses was found in 35 tumors, normal karyotypes in 145, and clonal chromosome aberrations were detected in 44. The three previously identified cytogenetic subgroups were all represented in this series: del(7) (q21.2q31.2) was found in 11, trisomy 12 in five, and t(12;14)(q14-15;q23-24) in one leiomyoma. Rearrangements of 6p, including deletions, inversions, and various translocations, were found in eight tumors, thus delineating a new cytogenetic subgroup of uterine leiomyoma. The remaining 21 karyotypically abnormal tumors had nonrecurrent changes. One leiomyoma had two cytogenetically unrelated clones characterized by del(7)(q21.2q31.2) and +12. Karyotypic changes in two separate leiomyomas from the same uterus were identified in five patients; in three of them, different anomalies were found in the two tumors, whereas cytogenetically identical aberrations - del(7q) and dic(21;22) - were detected in two macroscopically discrete tumors. These findings suggest that whereas some multiple leiomyomas originate independently, others may be derived from the same neoplastic clone.
本文呈现了对138例患者的224个平滑肌瘤的细胞遗传学分析结果。在35个肿瘤中发现有丝分裂数量不足,145个肿瘤核型正常,44个肿瘤检测到克隆性染色体畸变。此前确定的三个细胞遗传学亚组在本系列中均有体现:11个平滑肌瘤中发现del(7)(q21.2q31.2),5个中发现12三体,1个平滑肌瘤中发现t(12;14)(q14 - 15;q23 - 24)。在8个肿瘤中发现了6p的重排,包括缺失、倒位和各种易位,从而界定了子宫平滑肌瘤的一个新的细胞遗传学亚组。其余21个核型异常的肿瘤有非重复性改变。1个平滑肌瘤有两个细胞遗传学上不相关的克隆,特征分别为del(7)(q21.2q31.2)和 +12。在5例患者中,同一子宫的两个不同平滑肌瘤中发现了核型改变;其中3例患者的两个肿瘤有不同异常,而在两个肉眼可分辨的肿瘤中检测到细胞遗传学上相同的畸变——del(7q)和dic(21;22)。这些发现表明,一些多发性平滑肌瘤是独立起源的,而另一些可能源自同一个肿瘤克隆。