Crist W M, Ragab A H, Ducos R
Pediatrics. 1978 Apr;61(4):560-3.
A child presented with "acute leukemia" in which the blast cells resembled lymphoblasts and had negative cytochemical staining (PAS, Sudan black, and myeloperoxidase). Remission was induced and typical adult-type chronic myelogenous leukemia (CML) followed. Cytogenetic studies initially and during remission and subsequent "acute leukemia" relapses revealed the presence of the Philadelphia chromosome abnormality. Terminal transferase assay performed on peripheral blood blast cells was markedly elevated and soft agar culture growth parameters were typical of acute lymphoblastic leukemia T and B cell marker studies revealed no markers. This case report with supportive laboratory studies suggests that a cell line with lymphoid characteristics may predominate during acute leukemic transformation. This type of subclassification of leukemia may be of importance in therapeutic planning.
一名儿童被诊断为“急性白血病”,其原始细胞类似淋巴细胞,细胞化学染色(糖原染色、苏丹黑染色和髓过氧化物酶染色)均为阴性。诱导缓解后,发展为典型的成人型慢性粒细胞白血病(CML)。初始阶段、缓解期以及随后“急性白血病”复发时的细胞遗传学研究均显示存在费城染色体异常。对外周血原始细胞进行的末端转移酶检测显著升高,软琼脂培养生长参数符合急性淋巴细胞白血病的特征,T和B细胞标志物研究未发现标志物。本病例报告及相关实验室研究表明,在急性白血病转化过程中,具有淋巴细胞特征的细胞系可能占主导。这种白血病的亚分类在治疗方案制定中可能具有重要意义。