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Near tetrapoloid karyotype with translocation t(11;14) in a Moroccan patient with amyloid light-chain amyloidosis and multiple myeloma

机译:在摩洛哥患者中与甲蛋白轻链淀粉样蛋白症和多发性骨髓瘤的偶像T(11; 14)附近的四藻蛋白型。

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Cytogenetic and iFISH plays a major part in the diagnosis of the MM and have an important prognostic significance.10–15% of patients with amyloidosis will also have multiple myeloma (MM). Few studies have addressed the clinical and cytogenetic features of patients with AL amyloidosis with concurrent multiple myeloma.This study of MM case in which we found a near tetraploid complex karyotype with the t(11;14) (q13;q32) abnormality in cytogenetic analysis and the presence of t(4;14) and del(17p) by iFISH, referred to several studies which showed the translocation t(11;14) as the most frequent abnormality in both AL amyloidosis and MM.
机译:细胞遗传学和IFISH在MM的诊断中发挥着重要部分,并且具有重要的预后意义.10-15%的淀粉样变性患者也具有多种骨髓瘤(mm)。 少数研究已经解决了Al淀粉样蛋白病患者的临床和细胞遗传学特征,同时用多种骨髓瘤研究了MM情况的研究,其中我们发现近四倍体复合亚曲型与T(Q13; Q32)在细胞遗传学分析中异常 通过iFISH的T(4; 14)和Del(17p)的存在,提到了几种研究,该研究显示了易位T(11; 14)作为Al淀粉样蛋白病和MM中最常见的异常。

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