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Importance of FISH combined with Morphology, Immunophenotype and Cytogenetic Analysis of Childhood/Adult Acute Lymphoblastic Leukemia in Omani Patients

机译:鱼类的重要性与阿曼时期/成人急性淋巴细胞白血病儿童/成人急性淋巴细胞白血病的形态,免疫蛋白型和细胞遗传学分析

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Genetic changes associated with acute lymphoblastic leukemia (ALL) provide very important diagnostic and prognostic information with a direct impact on patient management. Detection of chromosome abnormalities by conventional cytogenetics combined with fluorescence in situ hybridization (FISH) play a very significant role in assessing risk stratification. Identification of specific chromosome abnormalities has led to the recognition of genetic subgroups based on reciprocal translocations, deletions and modal number in B or T-cell ALL. In the last twelve years 102 newly diagnosed childhood/adult ALL bone marrow samples were analysed for chromosomal abnormalities with conventional G-banding, and FISH (selected cases) using specific probes in our hospital. G-banded karyotype analysis found clonal numerical and/or structural chromosomal aberrations in 74.2% of cases. Patients with pseudodiploidy represented the most frequent group (38.7%) followed by high hyperdiploidy group (12.9%), low hyperdiploidy group (9.7%), hypodiploidy (46) group (9.7%) and high hypertriploidy group (3.2%). The highest observed numerical chromosomal alteration was high hyperdiploidy (12.9%) with abnormal karyotypes while abnormal 12p (7.5%) was the highest observed structural abnormality followed by t(12;21)(p13.3;q22) resulting in ETV6/RUNX1 fusion (5.4%) and t(9;22)(q34.1;q11.2) resulting in BCR/ABL1 fusion (4.3%). Interestingly, we identified 16 cases with rare and complex structural aberrations. Application of the FISH technique produced major improvements in the sensitivity and accuracy of cytogenetic analysis with ALL patients. In conclusion it confirmed heterogeneity of ALL by identifying various recurrent chromosomal aberrations along with non-specific rearrangements and their association with specific immunophenotypes. This study pool is representative of paediatric/adult ALL patients in Oman.
机译:与急性淋巴细胞白血病(All)相关的遗传变化为患者管理直接影响而提供非常重要的诊断和预后信息。通过常规细胞遗传学检测染色体异常联合荧光原位杂交(鱼)在评估风险分层方面发挥着非常重要的作用。特异性染色体异常的鉴定导致了基于B或T细胞中的互易转移,缺失和模态的遗传亚组识别。在过去的十二年中,在新诊断的儿童/成人中,分析所有骨髓样品,用常规G型G型常规G型染色体异常分析染色体异常,以及在医院中使用特定探针使用FISH(选定病例)。 G型核型分析发现克隆数值和/或结构染色体畸变在74.2%的情况下。具有假二叠片的患者代表最常见的基团(38.7%),然后是高超超倍细基团(12.9%),低超倍细基团(9.7%),低倍倍数(<46)组(9.7%)和高超倍增物组(3.2%)。观察到的数值染色体改变的最高高倍数(12.9%)具有异常的核型,而核型异常12p(7.5%)是观察到的结构异常最高,其次是T(12; 21)(p13.3; Q22)导致ETV6 / RUNX1融合(5.4%)和T(9; 22)(Q34.1; Q11.2)导致BCR / ABL1融合(4.3%)。有趣的是,我们确定了16例罕见和复杂的结构畸变。鱼类技术的应用产生了所有患者的细胞遗传学分析敏感性和准确性的重大改进。总之,通过鉴定各种复发染色体像差以及与特异性免疫胞间型相关的各种复发性染色体畸变来证实所有的异质性。这项研究池代表阿曼的所有患者的儿科/成人。

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