Warburg effect mimicking inborn errors of metabolism in childhood hematologic malignancies: A case-based systematic review

Khanittha Permtawee, Maliwan Tengsujaritkul, Chane Choed-Amphai, Supapitch Chanthong, Kanittha Mankhemthong, Lalita Sathitsamitphong, R. Natesirinilkul, P. Charoenkwan
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Abstract

BACKGROUND Type B lactic acidosis and hypoglycemia can occur in various pediatric conditions. In young children with a history of fasting preceding these metabolic derangements, inborn errors of metabolism should be primarily considered. However, the Warburg effect, a rare metabolic complication, can also manifest in children with hematologic malignancies. Only a few reports of this condition in children have been published in the literature. AIM To identify the clinical course, treatment strategies, and outcomes of childhood hematologic malignancies with type B lactic acidosis. METHODS We performed a comprehensive search of the PubMed, Scopus, and Cochrane databases without any time restriction but limited to English language articles. The databases were last accessed on July 1st, 2023. RESULTS A total of 20 publications were included in the analysis, all of which were case reports or case series. No higher quality evidence was available. Among children with hematologic malignancies and Warburg effect, there were 14 cases of acute lymphoblastic leukemia and 6 cases of non-Hodgkin’s lymphoma including our illustrative case. Lactic acidosis occurred in 55% of newly diagnosed cases and 45% of relapsed cases. The mean age was 10.3 ± 4.5 years, and 80% of cases were male. The mean serum lactate was 16.9 ± 12.6 mmol/L, and 43.8% of the cases had concomitant hypoglycemia. Lactic acidosis initially subsided in 80% of patients receiving chemotherapy compared to 60% in the contrast group. The mortality rate of newly diagnosed cases was 45.5%, while the relapsed cases represented a 100% mortality rate. All 8 patients reported before 2001 died from disease-related complications. However, patients described in reports published between 2003 and 2023 had a 54.5% rate of complete remission. CONCLUSION This complication has historically led to fatal outcome; however, patients who received chemotherapy showed a more favorable response. Therefore, it is crucial to promptly initiate specific treatment in this context.
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儿童血液系统恶性肿瘤中模仿先天性代谢错误的沃伯格效应:基于病例的系统回顾
背景:B型乳酸酸中毒和低血糖可发生在各种儿科疾病中。在这些代谢紊乱之前有禁食史的幼儿,应主要考虑先天性代谢错误。然而,Warburg效应,一种罕见的代谢并发症,也可以表现在儿童血液恶性肿瘤。文献中只有少数关于儿童这种情况的报道。目的探讨儿童血液恶性肿瘤合并B型乳酸酸中毒的临床过程、治疗策略和预后。方法:我们对PubMed、Scopus和Cochrane数据库进行了全面的检索,没有任何时间限制,但仅限于英文文章。数据库最后一次被访问是在2023年7月1日。结果共纳入20篇文献,均为病例报告或病例系列。没有更高质量的证据。在患有血液恶性肿瘤和Warburg效应的儿童中,有14例急性淋巴细胞白血病和6例非霍奇金淋巴瘤,包括我们的说明病例。55%的新诊断病例和45%的复发病例发生乳酸性酸中毒。平均年龄10.3±4.5岁,男性占80%。平均血清乳酸为16.9±12.6 mmol/L, 43.8%的患者伴有低血糖。接受化疗的患者中,乳酸酸中毒最初消退的比例为80%,而对照组为60%。新诊断病例死亡率为45.5%,复发病例死亡率为100%。2001年以前报告的所有8例患者均死于疾病相关并发症。然而,2003年至2023年间发表的报告中描述的患者完全缓解率为54.5%。结论该并发症历来可导致致命结局;然而,接受化疗的患者表现出更有利的反应。因此,在这种情况下,及时启动特异性治疗是至关重要的。
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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