Welborn Jeanna
Department of Internal Medicine and Pathology, University of California at Davis Medical Center Cancer Center, Room 3017, 4501 X Street, Sacramento, CA 95817 USA.
Cancer Genet Cytogenet. 2004 May;151(1):14-35. doi: 10.1016/j.cancergencyto.2003.09.019.
Robertsonian translocations are the most common constitutional structural abnormalities but are rarely reported as acquired aberrations in hematologic malignancies. The nonhomologous acrocentric rearrangements are designated as Robertsonian translocations, whereas the homologous acrocentric rearrangements are referred to as isochromosomes. Robertsonian rearrangements have the highest mutation rates of structural chromosome rearrangements based on surveys of newborns and spontaneous abortions. It would be expected that Robertsonian recombinations would be more common than suggested by the literature. A survey of the cytogenetics database from a single institution found 17 patients with acquired Robertsonian rearrangement and hematologic malignancies. This is combined with data from the literature for a total of 237 patients. All of the possible types of Robertsonian rearrangements have been reported in hematologic malignancies, with the i(13q), i(14q), and i(21q) accounting for nearly 60%. Complex karyotypic changes are seen in the majority of cases, corresponding with disease evolution. These karyotypes consistently show loss of chromosomes 5 and/or 7 in the myelocytic disorders, nonacrocentric isochromosomes, and centromeric breakage and reunion. However, nearly 25% of the acquired rearrangements were found as the sole abnormality or in addition to an established cytogenetic aberration. Most of these were the i(14q) with the myelodysplasia subtypes refractory anemia and chronic myelomonocytic leukemia.
罗伯逊易位是最常见的先天性结构异常,但在血液系统恶性肿瘤中作为获得性畸变却很少被报道。非同源近端着丝粒重排被称为罗伯逊易位,而同源近端着丝粒重排则被称为等臂染色体。根据对新生儿和自然流产的调查,罗伯逊重排在结构染色体重排中具有最高的突变率。预计罗伯逊重组会比文献中所提示的更为常见。对来自单一机构的细胞遗传学数据库进行的一项调查发现,有17例患有获得性罗伯逊重排和血液系统恶性肿瘤的患者。这与文献数据相结合,总计有237例患者。血液系统恶性肿瘤中已报道了所有可能类型的罗伯逊重排,其中i(13q)、i(14q)和i(21q)占近60%。在大多数病例中可见复杂的核型变化,这与疾病进展相对应。这些核型在髓细胞疾病中始终显示出5号和/或7号染色体缺失、非近端着丝粒等臂染色体以及着丝粒断裂和重聚。然而,近25%的获得性重排被发现是唯一的异常,或除了已确定的细胞遗传学畸变之外的异常。其中大多数是i(14q),与骨髓增生异常综合征亚型难治性贫血和慢性粒单核细胞白血病相关。