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Inadvertent transplantation of haematopoietic stem cells carrying constitutional Robertsonian translocation from an apparently normal donor to an AML patient: a case report.

机译:携带体质罗伯逊病易位的造血干细胞从表面正常供体无意间移植到AML患者:一例病例报告。

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摘要

Robertsonian translocations (RTs) are relatively common constitutional cytogenetic abnormalities involving the acrocentric chromosomes 13, 14, 15, 21 and 22. In subjects in whom RTs occur, there are no overt clinical consequences. RTs can also rarely be discovered in tumour cells obtained from some haematological malignant cases. In such cases they are acquired cytogenetic aberrations and almost always result in a trisomic karyotype that could contribute to clonal evolution of the underlying neoplastic disease. We report a case of transplantation of haematopoietic stem cells (HSCs) bearing RTs from an apparently healthy BM donor to a recipient with AML.
机译:罗伯逊易位(RTs)是相对常见的体质细胞遗传学异常,涉及acrocentric染色体13、14、15、21和22。在发生RTs的受试者中,没有明显的临床后果。从某些血液学恶性病例获得的肿瘤细胞中也很少发现RTs。在这种情况下,它们是获得性细胞遗传畸变,几乎总是导致三体核型,可能有助于潜在的肿瘤性疾病的克隆进化。我们报告了一个案例,即从具有明显健康的BM供体向带有AML的接受者移植带有RT的造血干细胞(HSC)。

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