Yao Ying, Wang Su-xia, Zhang You-kang
Renal Division, Department of Medicine, Peking University First Hospital; Institute of Nephrology, Peking University; Key Laboratory of Renal Diseases, Ministry of Health of China; Key Laboratory of Chronic Kidney Disease Prevention and Treatment, Ministry of Education of China; Beijing 100034, China.
Beijing Da Xue Xue Bao Yi Xue Ban. 2014 Oct 18;46(5):802-4.
Mutations in the fibrinogen Aα-chain genes are the most common cause of hereditary renal amyloidosis. The renal histologic appearance in the patient is characteristic and shows striking glomerular enlargement with almost complete obliteration of the normal glomerular architecture by extensive amyloid deposition. In contrast, the vessels and renal tubular interstitium of such patient contains almost no amyloid at all. Here, we described a patient with hereditary fibrinogen amyloidosis, who presented with proteinuria, hypertension and renal failure. He was shown to be heterozygous for the relevant mutation encoding the E526V fibrinogen variant.
纤维蛋白原Aα链基因突变是遗传性肾淀粉样变性最常见的病因。该患者的肾脏组织学表现具有特征性,显示肾小球显著增大,正常肾小球结构几乎被广泛的淀粉样蛋白沉积完全破坏。相比之下,这类患者的血管和肾小管间质几乎不含淀粉样蛋白。在此,我们描述了一名患有遗传性纤维蛋白原淀粉样变性的患者,他表现为蛋白尿、高血压和肾衰竭。他被证明是编码E526V纤维蛋白原变体的相关突变的杂合子。