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[菊池综合征、桥本甲状腺炎与狼疮血清学。附病例报告]

[Kikuchi syndrome, Hashimoto thyroiditis and lupus serology. Apropos of a case].

作者信息

Bousquet E, Tubéry M, Brousset P, Anzieu B, Dubarry B, Massip P, Duffaut M

机构信息

Service de médecine interne, CHU de Rangueil, Toulouse, France.

出版信息

Rev Med Interne. 1996;17(10):836-8. doi: 10.1016/0248-8663(96)82687-7.

Abstract

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.

摘要

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。

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