Park Borae G, Park Chan-Jeoung, Jang Seongsoo, Seo Eul Ju, Chi Hyun-Sook, Lee Jung-Hee
Department of Laboratory Medicine, University of Ulsan College of Medicine and Asan Medical Center, Seoul, Korea.
Korean J Lab Med. 2011 Apr;31(2):81-5. doi: 10.3343/kjlm.2011.31.2.81.
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.
急性髓系白血病复发为急性淋巴细胞白血病的情况鲜有报道。我们描述了一名62岁男性的病例,他被诊断为具有复杂核型的红白血病,诱导化疗后实现了完全血液学和细胞遗传学缓解。然而,在初次诊断4个月后,他出现复发,原始细胞呈现出不同的形态和免疫表型,被诊断为前体B细胞急性淋巴细胞白血病。复发的前体B细胞急性淋巴细胞白血病与原发性红白血病具有相同的白血病克隆。原发性红白血病时其骨髓的细胞遗传学分析显示存在复杂的核型异常,包括5号染色体单体和7号染色体单体。复发时,他的骨髓显示这些具有复杂核型异常的白血病克隆重新出现并伴有克隆转换。据我们所知,这是首例从红白血病转变为急性淋巴细胞白血病的谱系转换病例。