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A case of tubulointerstitial nephritis in IgG4-related systemic disease with markedly enlarged kidneys

机译:IgG4相关性全身疾病的肾小管间质性肾炎一例,肾脏明显肿大

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IgG4-related systemic disease, including autoimmune pancreatitis, is a multi-organ disorder characterized by elevated serum immunoglobulin G4 (IgG4) concentration and IgG4-positive plasma cell infiltration. We report the case of a 67-year-old man with IgG4-related tubulointerstitial nephritis, presenting with markedly enlarged kidneys and renal dysfunction. The serum IgG4 level was elevated with 4200?mg/dl and pathological examination revealed patchy, clearly fringed areas of IgG4-positive plasma cell infiltration and advanced fibrosis in the renal parenchyma, perirenal tissue and lymph nodes. With oral prednisolone at a dose of 60 mg daily, a contraction of the kidneys and an improvement of renal function were observed. No recurrence of the disease was observed during the reduction of prednisolone to 2 mg daily over 4 years.
机译:IgG4相关的全身性疾病,包括自身免疫性胰腺炎,是一种多器官疾病,其特征在于血清免疫球蛋白G4(IgG4)浓度升高和IgG4阳性浆细胞浸润。我们报道了一个67岁的IgG4相关性肾小管间质性肾炎的病例,其肾脏明显增大,肾功能不全。血清IgG4水平以4200?mg / dl升高,并且病理检查显示,在肾实质,肾周组织和淋巴结中,IgG4阳性浆细胞浸润的斑片,清晰的边缘区域和晚期纤维化。每天口服强的松龙剂量为60 mg,观察到肾脏收缩和肾功能改善。在泼尼松龙减至每天2 mg的4年中,未观察到该病的复发。

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