Department of Rheumatology and Immunology, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, 200127, China.
Department of Pathology, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, 200127, China.
BMC Pediatr. 2022 Nov 22;22(1):673. doi: 10.1186/s12887-022-03703-6.
Kikuchi-Fujimoto disease (KFD) is a self-limiting and benign disease characterized by cervical lymphadenopathy and fever. Although KFD should be made differentially diagnosed from infectious, autoimmune, and malignant diseases, it sometimes occurs in patients with systemic lupus erythematosus (SLE) and can be complicated with macrophage activation syndrome (MAS). However, it is rare that KFD is the initial manifestation of SLE and to be complicated with MAS.
A 9.6-year-old girl presented with high-grade fever, double-side cervical lymphadenopathy with mild pain of one week, leukopenia, alopecia, and rash on the cheek. During hospitalization, laboratory investigations showed positive antinuclear antibody (ANA), low complement 3 (C3), and low complement 4 (C4). Imaging investigations showed pleural and pericardial effusion. A 10.3-year-old girl presented with intermittent high-grade fever, double-sided cervical lymphadenopathy with obvious pain of 1-month duration, and discoid lesion on the cheek. During hospitalization, laboratory investigations showed positive ANA, leukopenia, thrombocytopenia, anemia with positive Coombs' test, low C3, and positive Smith antibodies. Both cases were diagnosed with KFD using lymph node biopsy, simultaneously fulfilling the diagnostic criteria of SLE. Subsequently, the two girls became complicated with MAS, followed by interstitial lung disease and neuropsychiatric lupus, respectively. Both patients benefited from high-dose methylprednisolone pulse therapy combined with intravenous cyclophosphamide.
More attention should be paid to differential diagnosis, especially SLE, in children diagnosed with KFD. In addition, children with SLE who presented with KFD as the initial manifestation seem to have a higher risk of developing MAS and experiencing organ involvement.
Kikuchi-Fujimoto 病(KFD)是一种自限性良性疾病,以颈部淋巴结病和发热为特征。尽管 KFD 应与感染性、自身免疫性和恶性疾病进行鉴别诊断,但它有时也会发生在系统性红斑狼疮(SLE)患者中,并可能并发巨噬细胞活化综合征(MAS)。然而,KFD 是 SLE 的初始表现并并发 MAS 则较为罕见。
一名 9.6 岁女孩因高热、双侧颈淋巴结痛伴轻度疼痛 1 周、白细胞减少、脱发和面颊皮疹就诊。住院期间,实验室检查显示抗核抗体(ANA)阳性、补体 3(C3)水平低和补体 4(C4)水平低。影像学检查显示胸腔和心包积液。另一名 10.3 岁女孩因间歇性高热、双侧颈淋巴结痛伴明显疼痛 1 个月和面颊盘状皮损就诊。住院期间,实验室检查显示 ANA 阳性、白细胞减少、血小板减少、贫血伴 Coombs 试验阳性、C3 水平低和 Smith 抗体阳性。两例均通过淋巴结活检诊断为 KFD,同时符合 SLE 的诊断标准。随后,两名女孩均并发 MAS,随后分别出现间质性肺病和神经精神性狼疮。两名患者均受益于大剂量甲基强的松龙脉冲治疗联合静脉注射环磷酰胺。
对于诊断为 KFD 的儿童,应更加注意鉴别诊断,尤其是 SLE。此外,以 KFD 为初始表现的 SLE 患儿似乎发生 MAS 和发生器官受累的风险更高。