A. Gračanin, Tea Mikula, Ivica Horvatić, Luka Torić, M. Golob, J. Dobša, Matea Liskij, Gabrijela Buljan, K. Draženović, Matej Nedić, D. Ljubanović, KRESIMIR Galešić
{"title":"Kidney involvement in adults with IgA vasculitis: experiences from Clinical Hospital Dubrava, Zagreb","authors":"A. Gračanin, Tea Mikula, Ivica Horvatić, Luka Torić, M. Golob, J. Dobša, Matea Liskij, Gabrijela Buljan, K. Draženović, Matej Nedić, D. Ljubanović, KRESIMIR Galešić","doi":"10.33004/reumatizam-67-2-8","DOIUrl":null,"url":null,"abstract":"Introduction: IgA vasculitis, formerly named henoch-schönlein purpura, is a systemic small-vessel vasculitis that occurs commonly in children, while in adults, the disease remains rare. It is characterised by non-thrombocytopenic palpable purpura, arthritis, arthralgia, kidney disease and gastrointestinal pain. This study aimed to determine clinical signs and symptoms, laboratory and pathohistological parameters and therapy of IgA vasculitis in adults with renal involvement, by conducting our research on a sample of patients of a tertiary referral hospital. Research subjects and methods: In this retrospective cohort study, patients treated at clinical hospital dubrava from 2011 to 2019 were included, who were diagnosed with IgA vasculitis, based on clinical, laboratory and pathohistological criteria. clinical and laboratory parameters, were determined through the use of methods commonly used in clinical practice. In patients with symptoms and signs of kidney involvement and after patients’ consent, kidney biopsy was performed, and analysed by light, immunofluorescence and electron microscopy. Results: twenty-two adults (12 m, 10 F), whose median age was 57, were included in our study. Palpable purpura and nephritis were present in all patients. Thirteen (59.1%) patients had arthralgia and five of them (22.5%) experienced abdominal pain. respiratory infection preceded vasculitis in six (27.3%) patients, six patients ((27.3%) were taking medications and got vaccinated prior to the occurrence of vasculitis, and in ten (45.4%) patients the predisposing factor was unknown. Asymptomatic hematuria was present in ten (47.6%), subnephrotic proteinuria in three (14.3%), nephrotic syndrome in nine (42.9%) and nephritic syndrome in three (14.3%) patients. According to the findings of kidney biopsy, which was performed on 18 patients, eleven (61.6%) had mesangial proliferation, fourteen Reumatizam 2020;67(2):83–92 https://doi.org/10.33004/reumatizam-67-2-8 professional paper struČni rad","PeriodicalId":76426,"journal":{"name":"Reumatizam","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reumatizam","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.33004/reumatizam-67-2-8","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: IgA vasculitis, formerly named henoch-schönlein purpura, is a systemic small-vessel vasculitis that occurs commonly in children, while in adults, the disease remains rare. It is characterised by non-thrombocytopenic palpable purpura, arthritis, arthralgia, kidney disease and gastrointestinal pain. This study aimed to determine clinical signs and symptoms, laboratory and pathohistological parameters and therapy of IgA vasculitis in adults with renal involvement, by conducting our research on a sample of patients of a tertiary referral hospital. Research subjects and methods: In this retrospective cohort study, patients treated at clinical hospital dubrava from 2011 to 2019 were included, who were diagnosed with IgA vasculitis, based on clinical, laboratory and pathohistological criteria. clinical and laboratory parameters, were determined through the use of methods commonly used in clinical practice. In patients with symptoms and signs of kidney involvement and after patients’ consent, kidney biopsy was performed, and analysed by light, immunofluorescence and electron microscopy. Results: twenty-two adults (12 m, 10 F), whose median age was 57, were included in our study. Palpable purpura and nephritis were present in all patients. Thirteen (59.1%) patients had arthralgia and five of them (22.5%) experienced abdominal pain. respiratory infection preceded vasculitis in six (27.3%) patients, six patients ((27.3%) were taking medications and got vaccinated prior to the occurrence of vasculitis, and in ten (45.4%) patients the predisposing factor was unknown. Asymptomatic hematuria was present in ten (47.6%), subnephrotic proteinuria in three (14.3%), nephrotic syndrome in nine (42.9%) and nephritic syndrome in three (14.3%) patients. According to the findings of kidney biopsy, which was performed on 18 patients, eleven (61.6%) had mesangial proliferation, fourteen Reumatizam 2020;67(2):83–92 https://doi.org/10.33004/reumatizam-67-2-8 professional paper struČni rad
简介:IgA血管炎,原名过敏性紫癜,是一种全身性小血管血管炎,常见于儿童,而在成人中,这种疾病仍然很罕见。其特征是非血小板减少性可触及紫癜、关节炎、关节痛、肾病和胃肠道疼痛。本研究旨在通过对三级转诊医院的患者样本进行研究,确定成人肾脏受累IgA血管炎的临床体征和症状、实验室和病理学参数以及治疗方法。研究对象和方法:在这项回顾性队列研究中,纳入了2011年至2019年在杜拉瓦临床医院接受治疗的患者,他们根据临床、实验室和病理学标准被诊断为IgA血管炎。临床和实验室参数是通过使用临床实践中常用的方法来确定的。在有肾脏受累症状和体征的患者中,在患者同意后,进行肾脏活检,并通过光、免疫荧光和电子显微镜进行分析。结果:22名成年人(12米,10英尺),中位年龄57岁,被纳入我们的研究。所有患者均出现可触摸性紫癜和肾炎。13名(59.1%)患者出现关节痛,其中5名(22.5%)患者出现腹痛。在6名(27.3%)患者中,呼吸道感染发生在血管炎之前,6名患者(27.4%)在血管炎发生之前正在服药并接种了疫苗,10名(45.4%)患者的易感因素未知。无症状血尿10例(47.6%),肾下蛋白尿3例(14.3%),肾病综合征9例(42.9%),肾病综合症3例(14.3%)。根据对18名患者进行的肾活检结果,11名(61.6%)患有系膜增生,14名Reumatizam 2020;67(2):83–92https://doi.org/10.33004/reumatizam-67-2-8专业论文结构Čni rad