Pediatric Acute Promyelocytic Leukemia

C. E., Verdú Belmar J, Garzó Moreno A, D. F
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Abstract

A previously healthy 4-year-old boy presented to the pediatric emergency department with high fever, headache, asthenia and neutropenia. The fever started two days prior along with the appearance of purple skin lesions. Laboratory results were as follows: White Blood Cell (WBC) count of 44.2 × 109 hemoglobin 62g/L; hematocrit 18.9%, platelet count 30 × 109/l, international normalized ratio (INR) 1.06, lactate dehydrogenase (LDH) 479u/l, creatinine 37μmol/l. Peripheral blood smear demonstrated: 80% of abnormal promyelocytes with bilobar nuclei and cytoplasmic granules; some contained multiple Auer rods. Immunophenotyping demonstrates CD13, CD33, CD117, and myeloperoxidase positivity with a high side-scatter. Fluorescence in situ hybridization revealed the t(15;17) (q22;q21.1) (PML-RARA) (Figure 1 and 2).
儿童急性早幼粒细胞白血病
一名先前健康的4岁男孩因高烧、头痛、乏力和中性粒细胞减少症到儿科急诊科就诊。两天前开始发烧,同时出现紫色皮肤病变。实验结果如下:白细胞计数为44.2×109血红蛋白62g/L;红细胞压积18.9%,血小板计数30×109/l,国际标准化比值(INR)1.06,乳酸脱氢酶(LDH)479u/l,肌酸酐37μmol/l。外周血涂片显示:80%的异常早幼粒细胞具有双叶核和细胞质颗粒;一些包含多个Auer棒。免疫表型显示CD13、CD33、CD117和髓过氧化物酶阳性,具有高侧散点。荧光原位杂交显示t(15;17)(q22;q21.1)(PML-RARA)(图1和2)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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