摘要
目的:分析IgG4相关性自身免疫性胰腺炎(immunoglobulin-G4 related autoimmune pancreatitis, IgG4-AIP)的临床特征。方法:本文报道1例AIP,就诊时患者伴有眼睑肿胀、糖尿病等症状,结合患者血清学及影像学检查拟诊为IgG4-AIP,予以2周激素治疗,胰腺肿块明显减小,确诊为IgG4-AIP。结果:患者经激素治疗后随访未复发。结论:IgG-AIP具有独特的血清学及影像学特征,激素治疗有效。
Objective: To analyze the clinical characteristics of immunoglobulin-G4 related autoimmune pancreatitis. Methods: A case of AIP was reported in this paper. The patient was suspected as IgG4-AIP by serological and imaging examination. The pancreatic mass decreased significantly after 2 weeks of steroid therapy, and the patient was diagnosed with IgG4-AIP. Results: There was no relapse after hormone therapy. Conclusion: IgG-AIP has unique serological and imaging characteristics, and steroid therapy is effective.
出处
《临床医学进展》
2022年第3期1876-1880,共5页
Advances in Clinical Medicine