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Cytogenetics of extramedullary manifestations in multiple myeloma

机译:多发性骨髓瘤髓外表现的细胞遗传学

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Extramedullary disease in patients with multiple myeloma is a rare event, occurring mostly in advanced disease or relapse. Outcome is poor and prognostic factors predicting the development of extramedullary disease have not been defined. We investigated cytogenetic alterations of myeloma cells in different extramedullary manifestations by adapting the fluorescence in situ hybridization (FISH) technique in combination with cytoplasmic immunoglobulin staining to study the cytogenetics of plasma cell tumours on paraffin embedded material. Thirty six patients were investigated: 19 with extramedullary disease, 11 with skeletal extramedullary disease and six with solitary extramedullary plasmacytoma. The first two groups showed the following results: del(17p13) 32% vs. 27%, del(13q14) 35% vs. 27%, MYC-overrepresentation 28% vs. 18% and t(4;14) 37% vs. 18%. We detected an overall higher incidence of del(17p13) in both groups compared to data from bone marrow samples of multiple myeloma reported to date (range 7-16%). The solitary extramedullary plasmacytomas presented overall less cytogenetic aberrations than the other groups. Most important, three patients with extramedullary disease and one with skeletal extramedullary disease presented different FISH findings in the extramedullary tumour compared to their bone marrow plasma cells. del(17p13), occurring additional in three of four cases, seems a strong marker for extramedullary progression of myeloma.
机译:多发性骨髓瘤患者的髓外疾病罕见,主要发生在晚期疾病或复发中。结果很差,尚未确定预测髓外疾病发展的预后因素。我们通过结合荧光原位杂交(FISH)技术和细胞质免疫球蛋白染色,研究了不同髓外表现的骨髓瘤细胞的细胞遗传学改变,以研究石蜡包埋材料上浆细胞瘤的细胞遗传学。调查了36例患者:19例髓外疾病,11例骨骼外髓疾病和6例孤立性髓外浆细胞瘤。前两组显示以下结果:del(17p13)32%vs. 27%,del(13q14)35%vs. 27%,MYC超额代表人数28%vs. 18%,t(4; 14)37%vs 18%与迄今报道的多发性骨髓瘤骨髓样本数据相比,我们在两组中检测到的del(17p13)总体发生率较高(范围为7-16%)。单独的髓外浆细胞瘤总体上比其他组少。最重要的是,与骨髓浆细胞相比,三名髓外疾病患者和一例骨骼外髓疾病患者在髓外肿瘤中表现出不同的FISH发现。 del(17p13)在4例中的3例中另外发生,似乎是骨髓瘤髓外进展的有力标志。

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