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机构地区:[1]哈尔滨医科大学附属第一医院肾内科,哈尔滨150001
出 处:《中国中西医结合肾病杂志》2010年第10期903-905,共3页Chinese Journal of Integrated Traditional and Western Nephrology
摘 要:目的:探讨原发性IgA肾病患者临床表现、病理特点及其相关性。方法:回顾性总结分析123例经肾活检病理确诊为原发性IgA肾病的临床和病理资料。结果:123例IgA肾病患者在21岁~40岁年龄段发病率最高(占65.8%);临床表现以发作性肉眼血尿最多见(占36.6%);病理类型分级以Ⅱ级(56.1%),Ⅲ级(20.3%)为主;病理类型与临床表现呈正相关(P<0.01);随着Lee氏病理分级程度的增高,血肌酐、血尿酸、血脂有不同程度的升高(P<0.05)。结论:IgA肾病临床类型多样,其组织形态学改变轻重不一,宜尽早做肾活检以明确诊断,指导治疗。Objective:To study the relationship between clinical manifestation and pathological feature with primary IgA nephropathy.Methods:The clinical and pathological data of 123 patients with primary IgA nephropathy diagnosed by renal biopsy were retrospectively analyzed.Results:The incidence of 123 IgA nephropathy was the highest in patients at the age of 21~40 years (65.8%).Clinically,IgA nephropathy of the paroxysmal gross hematuria type was the most common among the patients(36.6%).The pathological type Ⅱ was the most common (56.1%) followed by type Ⅲ(20.3%).Pathological type was positively correlated with the clinical manifestations(P0.01).Serum creatinine,serum uric acid and blood lipid levels increased with Lee’s pathological grade increasing (P0.05).Conclusion:IgA nephropathy had diverse clinical manifestations.Histomorphology changed with different severity.Early renal biopsy should be performed and appropriate therapy administered.
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