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多发性骨髓瘤的细胞遗传学研究

Cytogenetic study in multiple myeloma.

作者信息

Ferti A, Panani A, Arapakis G, Raptis S

出版信息

Cancer Genet Cytogenet. 1984 Jul;12(3):247-53. doi: 10.1016/0165-4608(84)90036-0.

Abstract

Ten patients with multiple myeloma (MM) were studied cytogenetically, using the G-banding technique. It was found that five patients had a normal karyotype, whereas five patients exhibited various chromosomal abnormalities. The presence of marker chromosomes was a consistent finding. Among those, the 14q+ marker chromosome was present in three cases, partial or complete trisomy for 1q was detected in four cases, and chromosome #6 was involved in two cases. In one case the 14q+ marker chromosome was determined to result from a translocation between chromosomes #11 and #14. In one patient with Bence Jones kappa multiple myeloma, there was a translocation between chromosomes #2 and #8.

摘要

采用G显带技术对10例多发性骨髓瘤(MM)患者进行了细胞遗传学研究。发现5例患者核型正常,而另外5例患者表现出各种染色体异常。标记染色体的存在是一个一致的发现。其中,3例存在14q+标记染色体,4例检测到1q部分或完全三体,2例涉及6号染色体。在1例中,确定14q+标记染色体是由11号和14号染色体之间的易位导致的。在1例本-周κ型多发性骨髓瘤患者中,2号和8号染色体之间存在易位。

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