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伴有先天性染色体异常的骨髓移植。细胞遗传学研究及临床意义。

Transplantation of bone marrow with constitutional chromosomal anomalies. Cytogenetic studies and clinical implications.

作者信息

Becher R, Mahmoud H K, Schaefer U W, Schmidt C G

出版信息

Blut. 1986 Oct;53(4):341-6. doi: 10.1007/BF00320894.

Abstract

We report on two cases of transplantation of bone marrow with constitutional chromosomal anomalies. A female patient with acute myelocytic leukemia (FAB, M 3) in first complete remission received a bone marrow graft from her sister with the karyotype 47 XXX (triple-X-syndrome). A male patient with Ph-positive CML and a constitutional Robertsonian t(14; 15) received HLA and MLC loci compatible bone marrow from his sister who was also a carrier of the Robertsonian t(14; 15). Our findings indicate that transplantation of marrow from donors with balanced chromosomal translocation is possible, although no conclusion can be made regarding long term results as both recipients died early from infectious complications.

摘要

我们报告了两例伴有先天性染色体异常的骨髓移植病例。一名处于首次完全缓解期的急性髓细胞白血病(FAB,M3)女性患者接受了来自其核型为47 XXX(三X综合征)的姐姐的骨髓移植。一名患有Ph阳性慢性粒细胞白血病且伴有先天性罗伯逊易位t(14; 15)的男性患者,接受了来自同样携带罗伯逊易位t(14; 15)的姐姐的HLA和MLC位点相匹配的骨髓。我们的研究结果表明,来自染色体平衡易位供者的骨髓移植是可行的,不过由于两名受者均因感染并发症过早死亡,因此无法得出关于长期结果的结论。

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