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A rare metabolic complication of acute lymphoblastic leukemia in childhood: Lactic acidosis

机译:儿童急性淋巴细胞白血病罕见的代谢并发症:乳酸性酸中毒

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摘要

A 13-year-old boy presented with nausea, fatigue, weight loss, and bone pain for two months. Complete blood count and serum renal and liver function tests were all normal. Blood gas analysis revealed severe metabolic acidosis with high anion gap. Lactate level was 61.2 mmol/L. Abdominal ultrasonography yielded bilateral nephromegaly and hepatomegaly with increased echogenicity. Peripheral blood smear revealed 2% blasts. Bone marrow aspiration showed 'Common ALL Antigen'-negative acute lymphoblastic leukemia by flow cytometric analysis. Metabolic acidosis dissolved as soon as chemotherapy was begun. Lactic acidosis at the presentation of acute lymphoblastic leukemia -especially with low tumor burden- is a very rare and almost always fatal complication. Our patient is still alive and in remission, which is a point of interest in this child.
机译:一个13岁的男孩表现出恶心,疲劳,体重减轻和骨痛两个月。全血细胞计数和血清肾,肝功能检查均正常。血气分析显示严重的代谢性酸中毒,阴离子间隙高。乳酸水平为61.2 mmol / L。腹部超声检查显示双侧肾肿大和肝肿大,回声增加。外周血涂片显示2%的爆炸。通过流式细胞术分析,骨髓穿刺显示“共同ALL抗原”阴性的急性淋巴细胞白血病。化疗开始后,代谢性酸中毒就消失了。急性淋巴细胞白血病(尤其是低肿瘤负荷)表现出的乳酸性酸中毒是非常罕见的,几乎总是致命的并发症。我们的病人还活着并且正在缓解,这是这个孩子的兴趣所在。

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