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一例对皮质类固醇和免疫抑制治疗反应异常的IgA肾病病例。

A case of IgA nephropathy with an unusual response to corticosteroid and immunosuppressive therapy.

作者信息

Abreo K, Wen S F

出版信息

Am J Kidney Dis. 1983 Jul;3(1):54-7. doi: 10.1016/s0272-6386(83)80010-9.

Abstract

We report a case of IgA nephropathy that presented with nephrotic syndrome without hematuria. Renal biopsy revealed typical features of IgA nephropathy on light microscopy, immunofluorescence microscopy, and electron microscopy. A dramatic response occurred on corticosteroid and immunosuppressive therapy, characterized by clearance of proteinuria and a fall of serum IgA level to normal. The absence of hematuria and a response to therapy are distinctly unusual features of IgA nephropathy. This case represents a variant of IgA nephropathy associated with a nephrotic syndrome that resembles nephrotic syndrome with minimal change lesion in its responsiveness to immunosuppressive therapy.

摘要

我们报告一例表现为无血尿的肾病综合征的IgA肾病病例。肾活检在光镜、免疫荧光显微镜和电子显微镜下显示出IgA肾病的典型特征。皮质类固醇和免疫抑制治疗产生了显著反应,表现为蛋白尿清除以及血清IgA水平降至正常。无血尿以及对治疗有反应是IgA肾病明显不寻常的特征。该病例代表了一种与肾病综合征相关的IgA肾病变体,其在对免疫抑制治疗的反应方面类似于微小病变型肾病综合征。

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