双表型急性白血病

K Lemhouer, J Elamouri, M. Braoul, I. tlamçani, M. Amrani Hassani
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摘要

双表型白血病(BAL)的定义是在相同的母细胞上存在属于至少两个不同系的标记。即使在文献中存在差异,其发病率估计也不到急性白血病病例的5%。母细胞的形态学方面是可变的,1/3的病例为淋巴母细胞,其他病例为成髓细胞。母细胞流式细胞术通过淋巴细胞和髓细胞标记物(L+M)或髓细胞标记物和淋巴细胞标记物(M+L)的共同表达来区分BAL。伴有淋巴标记物B和T (B+T)的BAL较为少见。常规细胞遗传学检查可以更频繁地突出成人的BAL型异常t(9;22)(q34;q11),儿童的t(12;21)(p13;q22)或11q23异常,而其他细胞遗传学异常则更为罕见。我们注意到对两例急性白血病的免疫表型的观察,以突出分类某些具有混合表型的急性白血病的困难,并强调生物学分析对这些白血病的表征和管理的互补性。
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Biphenotypic acute leukemia
Biphenypic leukemia (BAL) is defined by the presence on the same blastic cells of markers belonging to at least two different lines. The incidence is estimated at less than 5% of acute leukemia cases, even if there are disparities in the literature. The morphological aspects of blast cells are variable, aspects of lymphoblasts in 1/3 cases or myeloblasts in other cases. Blast cell flow cytometry distinguishes BAL with co-expression of lymphoid and myeloid markers (L+M) or myeloid markers with lymphoid markers (M+L). BAL with lymphoid markers B and T (B+T) are rarer. Conventional cytogenetic examination makes it possible to highlight more frequently in the BAL type anomalies t(9;22)(q34;q11) in adults, t(12;21)(p13;q22) in children or abnormalities in 11q23, more rarely other cytogenetic abnormalities. We note the observation of two cases of acute leukemia with their immunophenotypic profile in order to highlight the difficulty of classifying certain acute leukemia with a mixed phenotype and highlight the complementarity of biological analyses for characterization and management of these leukemias.
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