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作 者:韩畅 戴莉萍 田红军 陈新鹏 肖剑伟 HAN Chang;DAI Liping;TIAN Hongjun;CHEN Xinpeng;XIAO Jianwei(Department of Rheumatology,Shenzhen Futian Hospital for Rheumatic Disease,Shenzhen 518040,China)
机构地区:[1]深圳市福田区风湿病专科医院风湿科,广东深圳518040
出 处:《中国麻风皮肤病杂志》2023年第8期608-610,共3页China Journal of Leprosy and Skin Diseases
基 金:2022年度广东省中医药局中医药科研项目(编号:20221342)。
摘 要:患者,女,44岁。反复全身斑疹10年,加重1个月。既往经糖皮质激素、中药、维生素等治疗未见好转。唇腺组织病理活检见5个淋巴聚集灶,结合抗核抗体等相关检查诊断为干燥综合征、高球蛋白血症性紫癜、肾小管酸中毒I型可能,给予免疫吸附联合糖皮质激素、免疫抑制剂治疗后病情好转。A 44-year-old female presented with repeated systemic macular rash for 10 years,aggravated for 1 month.And no improvement was observed after previous treatment with glucocorticoid,traditional Chinese medicine,and vitamins.According to biopsy of labial gland tissue showed 5 lymphatic aggregation dryness combined with other examination of antinuclear antibodies,the diagnosis of Sjogren's syndrome,hyperglobulinemia purpura,and suspected diagnosis of renal tubular acidosis type I was made.After immunoadsorption combined with glucocorticoid and immunosuppressant treatment,the patient was improved.
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