Konoshita T, Okamoto K, Koni I, Mabuchi H
Second Department of Internal Medicine, School of Medicine, Kanazawa University, Japan.
Clin Nephrol. 1998 Aug;50(2):113-7.
Polycystic kidney disease (PKD) is one of important causes of end-stage renal disease (ESRD). However, there have been few detailed reports on PKD patients with ESRD. The present study was designed to clarify the clinical characteristics of PKD patients with ESRD.
We collected data from 22 renal divisions in our region, where 63 of 1246 patients with ESRD (male/female: 31/32) were proven to suffer from PKD (5.06%).
The average age at the induction of renal replacement therapy was 52.4 +/- 10.0 years. Of these patients, 32 (50.8%) had some family members with apparent PKD. Three (4.8%) and 4 (6.3%) had a history of subarachnoidal hemorrhage and intracerebral hemorrhage, respectively. One (1.6%) suffered from tuberous sclerosis. The prevalence of hypertension treated with antihypertensives, anemia treated with rHuEPO, hepatic cyst, pancreatic cyst, intracranial aneurysm and colonic diverticulum were 66.7%, 58.7%, 85.7%, 16.0%, 33.3% and 50.0%, respectively.
There was no marked difference in general characteristics or history between the present subjects and those described in previous reports. However, the prevalence of complications seemed to be higher than previously estimated.
多囊肾病(PKD)是终末期肾病(ESRD)的重要病因之一。然而,关于患有ESRD的PKD患者的详细报道较少。本研究旨在阐明患有ESRD的PKD患者的临床特征。
我们收集了本地区22个肾脏科室的数据,在1246例ESRD患者中,有63例(男/女:31/32)被证实患有PKD(5.06%)。
开始肾脏替代治疗时的平均年龄为52.4±10.0岁。在这些患者中,32例(50.8%)有一些家庭成员患有明显的PKD。分别有3例(4.8%)和4例(6.3%)有蛛网膜下腔出血和脑出血病史。1例(1.6%)患有结节性硬化症。接受抗高血压治疗的高血压、接受重组人促红细胞生成素治疗的贫血、肝囊肿、胰腺囊肿、颅内动脉瘤和结肠憩室的患病率分别为66.7%、58.7%、85.7%、16.0%、33.3%和50.0%。
本研究对象与既往报道的对象在一般特征或病史方面无明显差异。然而,并发症的患病率似乎高于先前的估计。