与特发性嗜酸性粒细胞增多综合征相关的膜性肾小球病。
Membranous glomerulopathy associated with idiopathic hypereosinophilic syndrome.
作者信息
Frigui Makram, Hmida Mohamed Ben, Jallouli Moez, Kechaou Manel, Frikha Faten, Bahloul Zouhir
机构信息
Department of Internal Medicine, Hedi Chaker Hospital, Sfax, Tunisia.
出版信息
Saudi J Kidney Dis Transpl. 2010 Mar;21(2):320-2.
Renal involvement is rarely reported and little is known about the renal morphologic changes in the idiopathic hypereosinophilic syndromes. We reported a case of a 52-year-old man with idiopathic hypereosinophilic syndrome associated with membranous glomerulopathy. The eosinophilia and the proteinuria greatly improved with corticosteroid treatment. We review the literature regarding the nephropathy of this hematologic disorder.
肾受累情况鲜有报道，对于特发性嗜酸性粒细胞增多综合征的肾脏形态学改变知之甚少。我们报告了一例52岁男性特发性嗜酸性粒细胞增多综合征合并膜性肾小球病的病例。经皮质类固醇治疗后，嗜酸性粒细胞增多和蛋白尿情况大为改善。我们回顾了关于这种血液系统疾病所致肾病的文献。
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