›› 2017, Vol. 37 ›› Issue (8): 733-735.

• 病案分析 • 上一篇    下一篇

口腔黏膜线状IgA大疱性皮病1例

尹艳娇1,郭明2,王茜3,丁欣欣1,葛翘诚1,吴佩玲1   

  1. 1. 新疆医科大学第二附属医院
    2. 新疆维吾尔治自区人民医院
    3. 中国医科大学附属口腔医院
  • 收稿日期:2017-01-11 修回日期:2017-03-11 出版日期:2017-08-28 发布日期:2017-08-28
  • 通讯作者: 吴佩玲 E-mail:wplkq@sina.com

One case report of oral linear IgA Bullous Dermatosis

  • Received:2017-01-11 Revised:2017-03-11 Online:2017-08-28 Published:2017-08-28

摘要: [摘要] 患者男,51岁。双侧上前牙唇侧牙龈破溃2个月,加重1周。病理诊断为类天疱疮。直接免疫荧光显示真表皮交界处IgA带状沉积,IgG、C3、IgM阴性。确诊为线状IgA大疱性皮病,给予糖皮质激素及沙利度胺联合治疗,取得良好效果。

关键词: 关键词:口腔黏膜, 线状lgA大疱性皮病, 免疫荧光

Abstract: Male patient, 51 years old. Double side to tooth lip side gum has burst 2 months, add 1 week. The pathological diagnosis of pemphigoid. DIF showed true epidermal junction the IgA banded deposition, IgG, C3, IgM negative. Diagnosed as linear IgA bullous skin disease, given glucocorticoid and thalidomide combination therapy, and achieved good results.

Key words: Key words: oral mucosa, Linear the lgA bullous skin disease, immunofluorescence

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