Leung Cheuk Cheung Derek, Chan Hiu Ching Christy, Chan Ming Chiu, Chan Yu Hong, Ho Man Ying, Chen Chun Hoi, Ngai Ching Man, Yeung Yiu Cheong
Department of Medicine and Geriatrics Princess Margaret Hospital Hong Kong.
Respirol Case Rep. 2024 Jun 19;12(6):e01414. doi: 10.1002/rcr2.1414. eCollection 2024 Jun.
Kikuchi-Fujimoto Disease (KFD), also known as Kikuchi disease or Kikuchi histiocytic necrotizing lymphadenitis, is a rare and self-limiting condition characterized by cervical lymphadenopathy and fever, primarily affecting young Asian adults. The aetiology of KFD remains unknown, although various infectious agents have been suggested as potential triggers. With the emergence of the COVID-19 pandemic, cases of post-COVID-19 KFD and post-COVID-19 vaccine KFD have been reported. In this article, we present the first case of post-COVID-19 KFD in Hong Kong. A 24-year-old man developed fever and painful neck swelling 1 month after recovering from COVID-19. Diagnostic evaluation, including ultrasound-guided fine needle aspiration cytology (FNAC), confirmed the diagnosis of KFD. The patient's symptoms resolved spontaneously with supportive care. This case underscores the importance of considering KFD as a potential differential diagnosis in patients presenting with cervical lymphadenopathy and fever following COVID-19 recovery or vaccination.
菊池-藤本病(KFD),也称为菊池病或菊池组织细胞坏死性淋巴结炎,是一种罕见的自限性疾病,其特征为颈部淋巴结病和发热,主要影响年轻的亚洲成年人。尽管有人提出各种感染因子可能是潜在诱因,但KFD的病因仍不清楚。随着新冠疫情的出现,已有新冠后KFD和新冠疫苗接种后KFD的病例报告。在本文中,我们介绍了香港首例新冠后KFD病例。一名24岁男性在新冠康复1个月后出现发热和颈部疼痛性肿胀。包括超声引导下细针穿刺细胞学检查(FNAC)在内的诊断评估确诊为KFD。患者的症状通过支持治疗自发缓解。该病例强调了在新冠康复或接种疫苗后出现颈部淋巴结病和发热的患者中,将KFD作为潜在鉴别诊断的重要性。