Brody J P, Krause J R, Kaplan S S, Penchansky L
South Med J. 1984 Nov;77(11):1461-4. doi: 10.1097/00007611-198411000-00026.
We have reported two cases of Philadelphia-chromosome-negative acute leukemia with heterogeneous populations of leukemic cells and reviewed six cases from the literature. The cases were identified by several methods, including morphology, cytochemistry, enzymatic analysis, cytogenetic analysis, and electron microscopy. Predisposing factors were probably present in three cases and may partially account for the seemingly increasing incidence, as has been the experience with other secondary leukemias. The prognosis was variable, but most of the complete remissions were seen only when lymphocytic and nonlymphocytic antileukemic chemotherapeutic regimes were used. The occurrence of these unusual acute leukemias strongly supports the concept of a lymphoid-myeloid stem cell.
我们报告了2例费城染色体阴性的急性白血病,其白血病细胞群体具有异质性,并复习了文献中的6例病例。这些病例通过多种方法进行鉴定,包括形态学、细胞化学、酶分析、细胞遗传学分析和电子显微镜检查。3例病例可能存在诱发因素,这可能部分解释了其发病率看似上升的现象,其他继发性白血病也有类似情况。预后各不相同,但大多数完全缓解仅在使用淋巴细胞和非淋巴细胞抗白血病化疗方案时出现。这些不寻常的急性白血病的发生有力地支持了淋巴样-髓样干细胞的概念。