Hoshikawa N, Shirasawa K, Niino H, Hasegawa N, Fukuzumi N
First Department of Pathology, Kyorin University School of Medicine, Tokyo, Japan.
Acta Pathol Jpn. 1988 Feb;38(2):193-207. doi: 10.1111/j.1440-1827.1988.tb01097.x.
In this report we present the autopsy findings of acute megakaryoblastic leukemia with tumor formation in a 2-year-old female infant with Down's syndrome. Chromosomal analysis of blast cells revealed constitutional anomaly of trisomy 21 and two other related types of abnormal clones. Flow cytometric examination revealed blast cells expressing Ia-like or HLA-DR antigens. Postmortem examination showed extensive infiltration of leukemic cells in most of the examined organs, including the bone marrow with myelofibrosis. Tumor masses in the maxillary, frontal and femoral bones and the atria of the heart had undergone massive infiltration of atypical blast cells with an increase in the reticulin network. The final diagnosis was confirmed by ultrastructural cytochemistry of the platelet peroxidase reaction as well as by immunological staining utilizing anti-platelet glycoprotein IIb/IIIa, antiplatelet factor 4 and anti-beta-thromboglobulin antibodies for the blast cells. It seems likely that platelet-derived growth factor, secondary to an increase in the reticulin network, plays a major role in myelofibrosis of acute megakaryoblastic leukemia with tumor formation.
在本报告中,我们呈现了一名患有唐氏综合征的2岁女婴急性巨核细胞白血病伴肿瘤形成的尸检结果。原始细胞的染色体分析显示存在21三体的先天性异常以及另外两种相关类型的异常克隆。流式细胞术检查显示原始细胞表达Ia样或HLA-DR抗原。尸检显示,在大多数检查的器官中存在白血病细胞的广泛浸润,包括伴有骨髓纤维化的骨髓。上颌骨、额骨和股骨以及心脏心房的肿瘤块已发生非典型原始细胞的大量浸润,网状纤维网络增加。通过血小板过氧化物酶反应的超微结构细胞化学以及利用抗血小板糖蛋白IIb/IIIa、抗血小板因子4和抗β-血小板球蛋白抗体对原始细胞进行免疫染色,最终确诊。继发于网状纤维网络增加的血小板衍生生长因子似乎在伴有肿瘤形成的急性巨核细胞白血病的骨髓纤维化中起主要作用。