Bousquet E, Tubéry M, Brousset P, Anzieu B, Dubarry B, Massip P, Duffaut M
Service de médecine interne, CHU de Rangueil, Toulouse, France.
Rev Med Interne. 1996;17(10):836-8. doi: 10.1016/0248-8663(96)82687-7.
Histiocytic necrotizing lymphadenitis (Kikuchi's disease) is an uncommon disease of the cervical lymph nodes occurring in young women, commonly associated with various auto-immune or infectious diseases. We describe the case of a 17 year-old girl who presented a Kikuchi's lymphadenitis occurring concomitantly with Hashimoto's thyroiditis and lupus serology as anti-nuclear, anti-DNA, anticardiolipid antibodies and hypocomplementemia. The patient was treated with prednisone and hydroxychloroquine. Thirty months after, she is doing well and hydroxychloroquine is continued.
组织细胞坏死性淋巴结炎（菊池病）是一种发生于年轻女性的颈部淋巴结罕见疾病，通常与各种自身免疫性或感染性疾病相关。我们描述了一名17岁女孩的病例，她同时患有菊池淋巴结炎、桥本甲状腺炎，狼疮血清学检查显示存在抗核抗体、抗双链DNA抗体、抗心磷脂抗体及低补体血症。该患者接受了泼尼松和羟氯喹治疗。30个月后，她病情好转，继续服用羟氯喹。
