Wang Tai-Ju, Yang Yao-Hsu, Lin Yu-Tsan, Chiang Bor-Luen
Department of Pediatrics, Cathay General Hospital, Taipei, Taiwan, ROC.
J Microbiol Immunol Infect. 2004 Aug;37(4):219-24.
Kikuchi-Fujimoto disease (KFD) is a rare cause of cervical lymphadenitis which mostly affects Asian women but is sometimes observed in the pediatric population. This study analyzed the clinical manifestations and disease course in children with KFD. Retrospective chart review and telephone interview were used to collect data for 13 children (8 boys and 5 girls) with a diagnosis of KFD from January 1988 to January 2003. Involvement of the posterior cervical lymph nodes was found in 12 patients, leukopenia in 9, and all patients had C-reactive protein less than 5 mg/dL. A high antinuclear antibody titer was associated with a more protracted and complicated course. Five of the 13 patients had new symptoms compatible with an autoimmune process during follow-up, with neurological symptoms the most common. In conclusion, the risk of evolution into an autoimmune syndrome in pediatric KFD patients is high, and careful long-term observation is mandatory.
菊池-藤本病(KFD)是一种罕见的颈部淋巴结炎病因,主要影响亚洲女性,但有时也见于儿童群体。本研究分析了儿童KFD的临床表现和病程。采用回顾性病历审查和电话访谈收集了1988年1月至2003年1月期间确诊为KFD的13名儿童(8名男孩和5名女孩)的数据。12例患者出现颈后淋巴结受累,9例出现白细胞减少,所有患者的C反应蛋白均低于5mg/dL。高抗核抗体滴度与病程更长、更复杂相关。13例患者中有5例在随访期间出现了与自身免疫过程相符的新症状,其中神经症状最为常见。总之,儿童KFD患者发展为自身免疫综合征的风险很高,必须进行仔细的长期观察。