Asinobi A O, Gbadegesin R A, Adeyemo A A, Akang E E, Arowolo F A, Abiola O A, Osinusi K
Dept of Paediatrics, University College Hospital, Ibadan, Nigeria.
West Afr J Med. 1999 Jul-Sep;18(3):203-6.
The histological findings in renal biopsy specimens obtained from 41 children with the nephrotic syndrome in Ibadan, Nigeria, between July, 1989 and June, 1996 are presented. The patients consisted of 26 male and 15 female children and their ages ranged from 2-13 years. The predominant histological type was membranoproliferative glomerulonephritis (MPGN) which occurred in 21 (51.2%). Membranous nephropathy and minimal change nephropathy (MCN) accounted for 4 (9.8%) patients each. The prevalence of MPGN was 33.3% in children less than 5 years of age compared with 56.2% amongst children who were > or = 5 years. All the three patients with MCN who were treated with a course of prednisolone had complete remission of the disease. It is concluded that MPGN is the predominant histological lesion seen in childhood nephrotic syndrome in Ibadan and that MCN remains an uncommon lesion. Therefore, renal biopsy is recommended as a prelude to a trial of steroid therapy in these patients since MCN (which is generally associated with steroid-responsiveness) is an uncommon finding among them.
本文呈现了1989年7月至1996年6月间在尼日利亚伊巴丹从41例肾病综合征患儿获取的肾活检标本的组织学检查结果。这些患者包括26名男童和15名女童,年龄在2至13岁之间。主要的组织学类型是膜增生性肾小球肾炎(MPGN),共21例(51.2%)。膜性肾病和微小病变肾病(MCN)各占4例(9.8%)。5岁以下儿童中MPGN的患病率为33.3%,而5岁及以上儿童中为56.2%。所有3例接受泼尼松龙疗程治疗的MCN患者疾病均完全缓解。结论是,MPGN是伊巴丹儿童肾病综合征中主要的组织学病变,而MCN仍然是一种罕见病变。因此,鉴于MCN(通常与对类固醇的反应性相关)在这些患者中是罕见发现,可以建议对这些患者进行肾活检,作为类固醇治疗试验的前奏。