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一名患有糖尿病肾病的患者出现过敏性紫癜。

Henoch-Schönlein purpura in a patient with diabetic nephropathy.

作者信息

Orfila C, Lepert J C, Modesto A, Pipy B, Suc J M

机构信息

INSERM CJF 91-07, CHU, Toulouse-Rangueil, France.

出版信息

Am J Kidney Dis. 1994 Sep;24(3):509-14. doi: 10.1016/s0272-6386(12)80910-3.

Abstract

A 46-year-old man presented with Henoch-Schönlein purpura and diabetic nephropathy. At 30 years of age, the patient had presented with an acute and severe nephritic syndrome with severe renal impairment. The renal function returned to normal 6 months after this first attack. At the age of 38 years, the patient was diagnosed as having type II diabetes and was treated with diet alone. At 44 years of age, a renal biopsy was performed because of proteinuria and hematuria. In this renal biopsy, mesangial expansion, medial arterial hyperplasia, and focal interstitial fibrosis were found to be present. Mesangial and subendothelial deposits of immunoglobulin A (IgA) were demonstrated by immunofluorescence. At 45 years of age, cutaneous vasculitis appeared, and at 47 years of age, the patient presented with necrotic purpura, non-insulin-dependent diabetes, renal impairment, proteinuria, and hematuria. A skin biopsy demonstrated leukocytoclastic skin vasculitis with IgA deposits in the arterial walls. A second renal biopsy was performed that showed diabetic glomerulosclerosis associated with a marked vascular and interstitial fibrosis. Mesangial and subendothelial deposits of IgA and C3 and linear IgG deposits along the glomerular basement membranes were demonstrated by immunofluorescence. Electron microscopy showed that the glomerular basement membranes were thickened; a fusion of foot processes was observed and electron-dense deposits were present in the widened mesangium. In summary, we describe a patient with a history of ancient glomerulonephritis who presented with an IgA mesangial nephropathy consistent with Henoch-Schönlein purpura associated with diabetic glomerulosclerosis.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

一名46岁男性患有过敏性紫癜和糖尿病肾病。该患者30岁时曾出现急性重症肾炎综合征并伴有严重肾功能损害,首次发作6个月后肾功能恢复正常。38岁时,患者被诊断为2型糖尿病,仅接受饮食治疗。44岁时,因蛋白尿和血尿进行了肾活检,在此次肾活检中发现存在系膜扩张、动脉中层增生和局灶性间质纤维化,免疫荧光显示系膜和内皮下有免疫球蛋白A(IgA)沉积。45岁时出现皮肤血管炎,47岁时患者出现坏死性紫癜、非胰岛素依赖型糖尿病、肾功能损害、蛋白尿和血尿。皮肤活检显示白细胞破碎性皮肤血管炎,动脉壁有IgA沉积。进行了第二次肾活检,显示糖尿病性肾小球硬化伴有明显的血管和间质纤维化,免疫荧光显示系膜和内皮下有IgA和C3沉积,沿肾小球基底膜有线性IgG沉积。电子显微镜显示肾小球基底膜增厚,观察到足突融合,增宽的系膜中有电子致密沉积物。总之,我们描述了一名有陈旧性肾小球肾炎病史的患者,其表现为与糖尿病性肾小球硬化相关的、符合过敏性紫癜的IgA系膜肾病。(摘要截短于250字)

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