作为前体b细胞淋巴细胞白血病复发的红白血病。

Borae G Park, Chan-Jeoung Park, Seongsoo Jang, Eul Ju Seo, Hyun-Sook Chi, Jung-Hee Lee
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引用次数: 10

摘要

AML复发为ALL的报道很少。我们描述了一个62岁的男子谁被诊断为红细胞白血病与复杂核型和实现完全血液学和细胞遗传学化疗后缓解。然而,在最初诊断4个月后,他复发,原始细胞表现出不同的形态和免疫表型,并被诊断为前体b细胞ALL。复发的前体b细胞ALL表现出与原发性红细胞白血病相同的白血病克隆。原发性红细胞白血病时骨髓细胞遗传学分析显示复杂的核型异常,包括单体5和单体7。在复发时,他的BM显示这些复杂核型异常的白血病克隆与克隆开关重新出现。据我们所知,这是第一例从红细胞白血病到ALL的谱系转换。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Erythroleukemia relapsing as precursor B-cell lymphoblastic leukemia.

Erythroleukemia relapsing as precursor B-cell lymphoblastic leukemia.

Erythroleukemia relapsing as precursor B-cell lymphoblastic leukemia.

Erythroleukemia relapsing as precursor B-cell lymphoblastic leukemia.

AML relapsing as ALL has rarely been reported. We describe the case of a 62-yr-old man who was diagnosed with erythroleukemia with a complex karyotype and achieved complete hematologic and cytogenetic remission after induction chemotherapy. However, 4 months after the initial diagnosis, he showed relapse with blasts showing a different morphology and immunophenotype and was diagnosed with precursor B-cell ALL. The relapsing precursor B-cell ALL presented with the same leukemic clones as the primary erythroleukemia. Cytogenetic analysis of his bone marrow (BM) at the time of the primary erythroleukemia showed complex karyotypic abnormalities, including monosomy 5 and monosomy 7. At relapse, his BM showed reemergence of these leukemic clones of complex karyotypic abnormalities with clonal switch. To our knowledge, this is the first case of a lineage switch from erythroleukemia to ALL.

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来源期刊
Korean Journal of Laboratory Medicine
Korean Journal of Laboratory Medicine 医学-医学实验技术
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