Ogg C S, Cameron J S, Williams D G, Turner D R
Clin Nephrol. 1981 Jan;15(1):9-13.
The case histories of nineteen patients who were seen in one renal unit between 1966 and 1978 and who were found to have primary amyloidosis are reviewed. Most were aged more than fifty and presented with the nephrotic syndrome without particular diagnostic features although electrophoresis of plasma and urine revealed abnormal immunoglobulins in a minority. Treatment was generally only symptomatic and most patients died within six months of diagnosis usually from renal failure. At the time of writing only the two patients treated by maintenance haemodialysis are still alive.
回顾了1966年至1978年间在一个肾脏科室就诊的19例原发性淀粉样变性患者的病历。大多数患者年龄超过50岁,表现为肾病综合征,无特殊诊断特征,尽管少数患者血浆和尿液电泳显示免疫球蛋白异常。治疗通常仅为对症治疗,大多数患者在诊断后六个月内死亡,通常死于肾衰竭。在撰写本文时,只有两名接受维持性血液透析治疗的患者仍然存活。