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风湿性多肌痛患者的继发性(AA型)淀粉样变性

Secondary (AA-type) amyloidosis in patients with polymyalgia rheumatica.

作者信息

Escribá A, Morales E, Albizúa E, Herrero J C, Ortuño T, Carreño A, Dominguez-Gil B, Praga M

机构信息

Nephrology Department, Hospital Universitario 12 de Octubre, Madrid, Spain.

出版信息

Am J Kidney Dis. 2000 Jan;35(1):137-40. doi: 10.1016/S0272-6386(00)70312-X.

Abstract

Several cases of systemic amyloidosis associated with polymyalgia rheumatica (PMR) or giant-cell arteritis (GCA) have been described. Nevertheless, the type of amyloid deposit has not been characterized in most of them. Here we report on two patients with PMR (one with associated GCA) who developed nephrotic syndrome and end-stage renal failure caused by massive amyloid deposition. Immunohistochemical analysis showed that the amyloid deposits were of AA type (secondary amyloidosis) in both cases.

摘要

已有多例系统性淀粉样变性与风湿性多肌痛(PMR)或巨细胞动脉炎(GCA)相关的病例报道。然而,其中大多数病例的淀粉样沉积物类型尚未明确。在此,我们报告两例PMR患者(其中一例合并GCA),他们因大量淀粉样沉积而发展为肾病综合征和终末期肾衰竭。免疫组织化学分析显示,两例患者的淀粉样沉积物均为AA型(继发性淀粉样变性)。

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