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Hemophagocytic syndrome in children with acute monoblastic leukemia - Another cause of fever of unknown origin

机译:急性单细胞白血病患儿的噬血细胞综合征-来历不明的另一种发热原因

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Purpose: Intensification of antileukemic treatment and progress in supportive management have improved the survival rates of children with acute myeloid leukemia (AML). However, morbidity and early mortality in these patients are still very high, especially in children with acute monoblastic leukemia (AML FAB M5). Inflammatory syndromes complicating the management of these children after application of cytosine arabinoside and due to hyperleukocytosis at initial presentation have been reported. Hemophagocytic lymphohistiocytosis (HLH) has been described as a serious and life-threatening acute complication during treatment of different oncologic entities; however, data on HLH in children with AML FAB M5 are extremely rare. Methods: A retrospective study of all children with AML FAB M5 treated at our institution between 1993 and 2013 was performed to describe the clinical characteristics of patients who developed an inflammatory syndrome with HLH during oncologic treatment. Results: Three of 10 children developed an inflammatory syndrome with fever, elevation of C-reactive protein, hyperferritinemia, elevation of soluble interleukin-2, and hemophagocytosis during prolonged aplasia following the first cycle of chemotherapy not responding to broad-spectrum antibiotics. No infectious agents could be identified; the initial symptoms occurred 17, 18, and 28 days after diagnosis of AML, respectively. The children immediately responded to dexamethasone; however, the same syndrome was observed again after the second cycle of chemotherapy and, in one patient, also after the third cycle. Conclusions: Treating physicians should be aware of an inflammatory syndrome resembling HLH in children with monoblastic leukemia since this problem might extremely complicate management and supportive care of these children. The co-incidence of monoblastic leukemia with HLH might be explained by cytokines released from the monoblastic leukemic cells themselves.
机译:目的:加强抗白血病治疗和支持治疗的进展已提高了急性髓细胞性白血病(AML)儿童的生存率。但是,这些患者的发病率和早期死亡率仍然很高,尤其是在患有急性单细胞白血病(AML FAB M5)的儿童中。据报导,在应用胞嘧啶阿糖苷后出现炎症综合症,使这些儿童的治疗复杂化,并且最初表现为白细胞增多。吞噬性淋巴细胞组织细胞增生症(HLH)被描述为治疗不同肿瘤实体时的严重且威胁生命的急性并发症。然而,AML FAB M5患儿的HLH数据极为罕见。方法:回顾性研究1993年至2013年间在我院接受治疗的所有AML FAB M5儿童的临床特征,以描述其在肿瘤治疗期间患有HLH炎性综合征的患者的临床特征。结果:10名儿童中的3名在长期不发育中,在对广谱抗生素无反应的化疗后的长时间发育不全中发炎,伴有发烧,C反应蛋白升高,高铁蛋白血症,可溶性白介素2升高和吞噬细胞。没有发现传染源;最初的症状分别在AML诊断后的17、18和28天出现。孩子们立即对地塞米松有所反应。但是,在第二个化疗周期后以及在第三个周期化疗后,再次观察到同一综合征。结论:治疗医生应注意单发性白血病儿童的类似HLH的炎症综合征,因为该问题可能会使这些儿童的管理和支持治疗极为复杂。单细胞白血病与HLH的并发可能是由单细胞白血病细胞本身释放的细胞因子所解释的。

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