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急性淋巴细胞白血病的免疫表型:摩洛哥卡萨布兰卡大学医院中心的经验。

Immunophenotype of Acute Lymphoblastic Leukemia: The Experience of University Hospital Centre Casablanca - Morocco.

出版信息

Clin Lab. 2023 Sep 1;69(9). doi: 10.7754/Clin.Lab.2023.230307.

Abstract

BACKGROUND

Acute lymphoblastic leukemia (ALL) encompasses a group of lymphoid neoplasms that morphologically and immunophenotypically resemble B-lineage and T-lineage precursor cells. Our objective is to describe the immunophenotypic aspects of acute lymphoblastic leukemia (All) diagnosed by flow cytometry at the hematology laboratory of IBN ROCHD University Hospital Center and to compare them with those reported in other series.

METHODS

This is a descriptive study over a period from August 2016 to October 2021, during a 5 year-and-2-month period. Immunophenotyping was performed at the flow cytometry unit on a Beckman-Coulter with 6 colors and 2 lasers in the hematology laboratory of the same hospital and data was collected retrospectively from the patients' files, their medical prescription files, kalisil software, and a data collection form we have established.

RESULTS

The 440 patients had ages ranging from 1 month to 76 years, with a median of 9.5 years and the overall male-to-female ratio was 1.44. The immunological subtyping revealed that 82.5% of cases were B-ALL and 17.5% were T-ALL; of these B-ALL cases 230 (63.36%) were children (range: 0.1 - 15 years) and 134 (36.91%) were adults (range: 16 - 76 years); T-ALL were distributed in both age groups, 49 cases (37.7%) were children (range: 2 - 15 years) and 28 (21.56%) were adults (range: 18 - 63 years). All patients presented at least one abnormal blood count; thrombocytopenia has been observed in 89.4% of cases, anemia in 86.5% of cases, hyperleukocytosis in 79.8% of cases, leukopenia in 10.6% of cases, and pancytopenia in 4.8% of cases. The frequency of B-cell markers in B-ALL was found to be 363 (100%) for CD19, 323 (88.94%) for CD10, 290 (80%) for CD79a, and 73 (20%) for CD20. CD34 expression was found in 73 (20%) cases of B-ALL. HLA-DR was found in 54 (15%) cases, while TdT was found in 43 (13%) cases. Aberrant expression of myeloid antigens was found in 94 (26%) cases of B-ALL. Among T-ALL, the positivity of CD3 and CD7 was 100% (77 cases), while CD5 was positive in 58 (75%) cases. CD34 expression was found in only 19 cases of T-ALL. CD4 and CD8 expression was checked in only 9 adult patients and 4 pediatric cases. Out of them, 77.82% of cases were negative for both CD4 and CD8. CD4 and CD8 double positivity was seen in only 11.1% of cases, and 22.4% of cases showed either CD4 or CD8 positivity.

CONCLUSIONS

We concluded that our study was similar to reports in the Americas and Europe, and it was the first large one that describes the immunophenotypic profile of ALL in the Moroccan population.

摘要

背景

急性淋巴细胞白血病(ALL)是一组形态学和免疫表型上类似于 B 谱系和 T 谱系前体细胞的淋巴肿瘤。我们的目的是描述在 IBN ROCHD 大学医院中心血液学实验室通过流式细胞术诊断的急性淋巴细胞白血病(ALL)的免疫表型特征,并将其与其他系列报告进行比较。

方法

这是一项描述性研究,时间跨度为 2016 年 8 月至 2021 年 10 月,为期 5 年零 2 个月。免疫表型分析在同一医院的流式细胞术单元上进行,使用 Beckman-Coulter 仪器,有 6 种颜色和 2 种激光,数据从患者档案、他们的处方档案、kalisil 软件和我们建立的数据收集表中回顾性收集。

结果

440 名患者年龄从 1 个月到 76 岁不等,中位数为 9.5 岁,总体男女比例为 1.44。免疫学分型显示 82.5%的病例为 B-ALL,17.5%为 T-ALL;其中 B-ALL 病例中有 230 例(63.36%)为儿童(范围:0.1-15 岁),134 例(36.91%)为成人(范围:16-76 岁);T-ALL 分布在两个年龄组,49 例(37.7%)为儿童(范围:2-15 岁),28 例(21.56%)为成人(范围:18-63 岁)。所有患者均至少有一项异常血象;89.4%的病例存在血小板减少症,86.5%的病例存在贫血,79.8%的病例存在白细胞增多症,10.6%的病例存在白细胞减少症,4.8%的病例存在全血细胞减少症。在 B-ALL 中,B 细胞标志物的频率为 CD19 为 363(100%),CD10 为 323(88.94%),CD79a 为 290(80%),CD20 为 73(20%)。CD34 表达在 73(20%)例 B-ALL 中发现。HLA-DR 在 54 例(15%)病例中发现,而 TdT 在 43 例(13%)病例中发现。在 94(26%)例 B-ALL 中发现髓系抗原异常表达。在 T-ALL 中,CD3 和 CD7 的阳性率为 100%(77 例),而 CD5 阳性率为 75%(58 例)。仅在 19 例 T-ALL 中发现 CD34 表达。仅在 9 例成年患者和 4 例儿科患者中检查了 CD4 和 CD8 的表达。其中,77.82%的病例均为 CD4 和 CD8 双阴性。仅 11.1%的病例出现 CD4 和 CD8 双阳性,22.4%的病例出现 CD4 或 CD8 阳性。

结论

我们得出结论,我们的研究与美洲和欧洲的报告相似,是第一个描述摩洛哥人群 ALL 免疫表型特征的大型研究。

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