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首页> 外文期刊>Frontiers in Pediatrics >Severe Recurrent Fever Episodes With Clinical Diagnosis of Hemophagocytic Lymphohistiocytosis, Incomplete Kawasaki Disease and Systemic-Onset Juvenile Idiopathic Arthritis: A Case Report and Literature Review
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Severe Recurrent Fever Episodes With Clinical Diagnosis of Hemophagocytic Lymphohistiocytosis, Incomplete Kawasaki Disease and Systemic-Onset Juvenile Idiopathic Arthritis: A Case Report and Literature Review

机译:严重的复发热发作患者临床诊断血糖淋巴管症,不完全川崎疾病和全身性发病性关节炎:案例报告和文献综述

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The pathogeneses of recurrent fever are quite complicated when excluding repeated infections. Recurrent fever is a common symptom for autoinflammatory diseases, relapse of Systemic-onset juvenile idiopathic arthritis (SoJIA) and recurrent Kawasaki disease (KD). There are no specific diagnostic laboratory tests for the diseases. Some studies showed that KD was the precursor of hemophagocytic lymphohistiocytosis (HLH). Macrophage activation syndrome (MAS) is another form of HLH in SoJIA. Cytokine disturbances are considered to be involved in the pathogenesis of the diseases. We describe a Chinese female toddler that developed three separate fever episodes with eventual diagnose of SoJIA over about 10 months. The first episode was diagnosed as IKD, immunoglobulin nonresponsive KD, and HLH. The second and third episodes were diagnosed as IKD and SoJIA, respectively. The fever was hard to be relieved by antipyretics, and the peak axillary temperature was above 40°C. For every fever episode, infections were excluded. For the first episode, trends over time of hemoglobin, platelets, fibrinogen, and triglycerides indicated HLH, which was finally diagnosed and treated according to the HLH-2004 protocol. For the second episode six months later, after excluding an HLH relapse and infections, IKD was finally diagnosed. Oral aspirin was administered, and the HLH treatment was ceased. The third episode occurred three months later, and SoJIA was finally diagnosed. For each episode, except for relative tests, we only tested for cytokines interleukin-1β, interleukin-6, and interferon-γ, due to limited laboratory test availability. These cytokines were elevated during remission and rose much higher in the fever phases. The case showed the difficulty to differentiating the recurrent fever in clinical practice. Surveillance of routine laboratory parameters over time might reveal a trend that indicates possible disease, even when parameter values do not meet diagnostic criteria. Changes in cytokine profiles are promising markers for differentiating recurrent fever diseases in future. An unknown immunological defect for the case may contribute to the recurrent immunological insults, and we are following up the recurrence of fever episode.
机译:在排除重复的感染时,复发热的病因非常复杂。复发发烧是自身炎症性疾病的常见症状,全身发作的幼年特发性关节炎(Sojia)和复发性川崎病(KD)。疾病没有具体的诊断实验室测试。一些研究表明,KD是血糖淋巴淋巴胞菌(HLH)的前体。巨噬细胞激活综合征(MAS)是Sojia的另一种形式的HLH。细胞因子干扰被认为参与疾病的发病机制。我们描述了一位中国女小孩,开发了三个独立的发热剧集,最终诊断了Sojia超过约10个月。第一集被诊断为IKD,免疫球蛋白非响应KD和HLH。第二次和第三集分别被诊断为IKD和Sojia。通过退化液难以缓解发烧,并且峰值腋中温度高于40℃。对于每次发烧发作,排除了感染。对于第一种发作,随着时间的推移,血红蛋白,血小板,纤维蛋白原和甘油三酯的时间随着时间的推移表示HLH,最终根据HLH-2004方案诊断和处理。对于六个月后的第二集,在排除了HLH复发和感染后,最终诊断出IKD。施用口服阿司匹林,停止HLH处理。第三集发生在三个月后,最终诊断出Sojia。对于每次发作,除相对测试外,由于有限的实验室测试可用性,我们仅测试了细胞因子白细胞介素-1β,白细胞介素-6和干扰素-γ。这些细胞因子在缓解期间升高,发热阶段的缓解率高得多。这种情况表明难以区分临床实践中的复发性。随着时间的推移,常规实验室参数的监测可能揭示了表明可能疾病的趋势,即使参数值不符合诊断标准。细胞因子型材的变化是未来分化复发性发热疾病的有希望的标志物。案例的未知免疫缺陷可能有助于复发性免疫损伤,我们正在追加发烧发作的复发。

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