幼儿川崎综合征:临床病例

V. Sokolovskaya, A. A. Litvinova, A. V. Krikova, R. S. Kozlov
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引用次数: 0

摘要

川崎综合征(SC)和儿童多系统炎症综合征(MIS-C)是医生难以诊断和治疗的炎症。这是两种不同的病症,尽管它们的许多特征具有共同之处。导致 SC 发病的复杂病理机制在临床上表现为人体大量功能系统的衰竭。目的:证明在 8 个月大的幼儿身上诊断川崎综合征的难度。结果。重点是中毒-发热、呼吸道、肠道、缺血性综合征在临床上占主导地位,以及在疾病的早期阶段心血管系统没有特殊症状,这给早期诊断带来了困难。结论我们介绍的临床病例表明,川崎综合征的发展不典型,心血管系统长期没有变化
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kawasaki syndrome in a young child: clinical case
Kawasaki syndrome (SC) and multisystem inflammatory syndrome in children (MIS-C) are inflammatory conditions that are difficult for doctors to diagnose and treat. These are two different states, despite the fact that many of their features have common features. Complex pathogenetic mechanisms that cause the development of SC find their clinical expression in the defeat of a large number of functional systems of the body. The aim: demonstrating the difficulty of diagnosing Kawasaki syndrome in a young child of 8 months. Results. The emphasis is placed on the clinical predominance of intoxication-febrile, respiratory, intestinal, exanthemic syndromes, as well as on the absence of specific symptoms from the cardiovascular system in the early stages of the disease, which made early diagnosis difficult. Conclusion. The clinical case we have presented demonstrates the atypical development of Kawasaki syndrome with a prolonged absence of changes from the cardiovascular system
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