Department of Internal Medicine, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan.
Department of Pathology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan.
Clin Exp Nephrol. 2011 Oct;15(5):774-779. doi: 10.1007/s10157-011-0483-4. Epub 2011 Jul 5.
Although the majority of renal amyloidosis is caused by either acquired monoclonal immunoglobulin light-chain amyloidosis or reactive systemic amyloid A, some cases are caused by hereditary amyloidosis. Apolipoprotein A-II (apoAII) amyloidosis is a rare form of hereditary amyloidosis and cannot be diagnosed by a routine examination. Thus, the prevalence and etiology of apoAII amyloidosis are uncertain. In humans, a genetic mutation in the stop codon of apoAII is considered to be a cause of amyloid fibril formation. We report on a 68-year-old man who presented with proteinuria by apoAII amyloidosis without family history. His proteinuria gradually increased to 6 g/day within 1 year. A renal biopsy showed amyloid deposition in the glomeruli, however, acquired monoclonal immunoglobulin light-chain amyloidosis and reactive systemic amyloid A were ruled out. Immunohistochemistry revealed apoAII deposition in the glomeruli, but DNA sequencing did not identify any genetic mutation in the coding sequence of apoAII. Here, we report a case of apoAII amyloidosis without a genetic mutation in the coding sequence and discuss the etiology of apoAII amyloidosis.
虽然大多数肾淀粉样变性是由获得性单克隆免疫球蛋白轻链淀粉样变性或反应性系统性淀粉样 A 引起的,但有些病例是由遗传性淀粉样变性引起的。载脂蛋白 A-II(apoAII)淀粉样变性是一种罕见的遗传性淀粉样变性形式,不能通过常规检查诊断。因此,apoAII 淀粉样变性的患病率和病因尚不确定。在人类中,apoAII 终止密码子的基因突变被认为是淀粉样纤维形成的原因。我们报告了一例 68 岁男性,因 apoAII 淀粉样变性出现蛋白尿,无家族史。他的蛋白尿在 1 年内逐渐增加到 6g/天。肾活检显示肾小球中有淀粉样物质沉积,但排除了获得性单克隆免疫球蛋白轻链淀粉样变性和反应性系统性淀粉样 A。免疫组化显示肾小球中有 apoAII 沉积,但 DNA 测序未发现 apoAII 编码序列中的任何基因突变。在此,我们报告一例无 apoAII 编码序列基因突变的 apoAII 淀粉样变性病例,并讨论 apoAII 淀粉样变性的病因。