Multisystem Inflammatory Syndrome in Adults Accompanied with Kikuchi-Fujimoto Disease

Eriko Kashihara, K. Doi, K. Fujita
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引用次数: 1

Abstract

We herein report a case of multisystem inflammatory syndrome in adults (MIS-A) complicated with Kikuchi-Fujimoto disease (KFD). A previously healthy 41-year-old man presented with painful swelling of the cervical lymph nodes, fever, diarrhea, conjunctivitis, edema, and hypotension one month after the onset of asymptomatic coronavirus disease 2019. Laboratory investigations revealed an elevation of CRP, and echocardiography indicated diastolic dysfunction. We diagnosed the patient to have MIS-A. Histopathology of the lymph nodes showed necrotizing lymphadenitis. After the initiation of hydrocortisone and diuretics, his symptoms resolved immediately. This case suggested that post-viral immune dysregulation in MIS-A could play a role in the etiology of KFD.
成人合并菊池-藤本病的多系统炎症综合征
我们在此报告一例成人多系统炎症综合征(MIS-A)合并菊池-藤本病(KFD)。一名41岁的健康男性,在2019年无症状冠状病毒病发病一个月后出现颈部淋巴结疼痛肿胀、发烧、腹泻、结膜炎、水肿和低血压。实验室检查显示CRP升高,超声心动图显示舒张功能障碍。我们诊断病人患有misa。淋巴结组织病理学显示坏死性淋巴结炎。在开始使用氢化可的松和利尿剂后,他的症状立即消失。本病例提示,病毒后免疫失调的misa可能在KFD的病因中发挥作用。
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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