Payne C M, Harrow E J
Am J Clin Pathol. 1983 Aug;80(2):216-23. doi: 10.1093/ajcp/80.2.216.
An unusual case of acute myelomonocytic leukemia (AMML) in an 81-year-old man is described. Ultrastructural examination revealed the presence of distinct Auer bodies, which commonly are found in acute promyelocytic leukemia (APL). The Auer bodies had a splinterlike appearance with a distinct tubular substructure. The morphologic appearance of the leukemic cells coupled with the results of cytochemical staining reactions (alpha-naphthyl AS-D chloroacetate esterase, alpha-naphthyl butyrate esterase, Sudan black B, and periodic acid-Schiff reaction) identified this leukemia as myelomonocytic in origin. APL-like Auer rods in AMML now can be included in the spectrum of morphologic forms commonly seen in myelogenous leukemia and lends support to the hypothesis of an aberrant stem cell. In addition to the APL-like Auer rods, the leukemic blasts contained giant pink-staining granules on Wright's stain, some of which had a tubular substructure similar to the Auer rods under the electron microscope. The presence of these megagranules is a morphologic aberration termed "the pseudo-Chediak-Higashi anomaly of acute leukemia," and now has been described for the first time in AMML at the ultrastructural level.
本文描述了一名81岁男性急性粒单核细胞白血病(AMML)的罕见病例。超微结构检查发现存在特征性的Auer小体,其通常见于急性早幼粒细胞白血病(APL)。Auer小体呈裂片样外观,具有独特的管状亚结构。白血病细胞的形态学表现以及细胞化学染色反应(α-萘基AS-D氯乙酸酯酶、α-萘基丁酸酯酶、苏丹黑B和过碘酸-希夫反应)的结果确定该白血病起源于粒单核细胞。AMML中APL样Auer棒现在可纳入髓系白血病常见形态学形式的范畴,并支持异常干细胞的假说。除了APL样Auer棒外,白血病原始细胞在瑞氏染色下含有巨大的粉红色颗粒,其中一些在电子显微镜下具有与Auer棒相似的管状亚结构。这些巨大颗粒的存在是一种形态学异常,称为“急性白血病的假性Chediak-Higashi异常”,目前已在AMML中首次在超微结构水平上被描述。