Schistosomiasis Associated Glomerulopathy (Glomerulonephristis / Nephrotic Syndrome): A review and Update of the Literature

A. Venyo
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Nevertheless, there are a number of patterns of renal involvement in Schistosomiasis which include (a) upper urinary tract sequelae of lower urinary tract Schistosomiasis pathology, (b) immune-related glomerulonephritis, (c) as well as oxidant-stress-mediated renal tubular glomerulonephritis. The renal involvement by Schistosomiasis does tend to be ensued by the development of Schistosomiasis-associated Glomerulopathy (Glomerulonephritis / Nephrotic Syndrome) of varying severity. Individuals affected by Schistosomiasis-associated kidney disease may develop (a) asymptomatic disease which tends to related to self-limited and asymptomatic glomerular disease (b) symptomatic disease which most commonly would tend to present with nephrotic syndrome most often in patients who develop hepato-splenic schistosomiasis with liver fibrosis associated with Schistosoma mansoni infection. Symptomatic patients tend to develop severe hypo-proteinemia, half of the patients tend to have elevated blood pressure. In the absence of nephrotic syndrome, patients who have Schistosomiasis-associated glomerulopathy may manifest with: (a) isolated non-nephrotic syndrome proteinuria (b) acute glomerulonephritis associated with haematuria and heavy proteinuria, (c) Nephrotic syndrome together with systemic manifestations of co-infection with salmonella (class II) or hepatitis C virus (Class I), (d) End stage renal disease (ESRD). Some of the patients who have Schistosomiasis of the kidney may present with Haematuria, Hypertension, Hepato-splenic Schistosomiasis. The diagnosis should be suspected with regard to the following scenarios: (a) clinical suspicion in a patient with kidney disease who is known or has been known to have Schistosoma mansoni; (b) exposure to an endemic area, (c) clinical evidence / demonstration of chronic hepatosplenic schistosomiasis, (d) if the patient has not been diagnosed as having been afflicted with schistosomiasis, then schistosomal infection should be documented, (e) majority of patients with schistosomiasis and kidney disease should have kidney biopsy. (f) The patients should be evaluated for co-infection with salmonella, hepatitis C virus, and hepatitis B virus in order to ensure adequate treatment of the disease. Schistosomiasis is the second most devastating tropical parasitic disease globally which tends to be responsible for many urological complications. Nevertheless, glomerular injury is an uncommon complication which has mainly or most often described with Schistosoma Mansoni. When patients who have Schistosomiasis-associated Kidney disease are managed and followed-up on long-term basis with renal end points, one third of the patients independent of the histopathology examination features of the kidney biopsies would tend to progress dialysis. Membranoproliferative glomerulonephritis (MPGN) is an uncommon complication associated with Schistosoma Haematobium infection which tends to be associated with potentially poor prognosis. MPGN could lead quickly to End Stage Renal Disease (ESRD). Anti-helminthic and immunosuppressive medicaments tend not to be effective at advanced stages of the disease and hence efforts need to be focused upon the prevention, early detection, as well as treatment of Schistosoma infections among at-risk groups of individuals. In order to reduce morbidity related to Schistosoma-associated nephropathy, public health policy, should be concentrated upon the prevention of the disease by the control of snail, improved sanitation, and health education, as well as by the implementation, and sustenance of chemotherapy-based control strategies. Considering that many individuals are found yearly to be inflicted by Schistosomiasis who tend to dwell in more rural parts of their countries where facilities for the undertaking of renal function tests and biopsies of the kidney tend not to be readily available, there is the likelihood that Schistosomiasis-associated nephropathies may be highly underdiagnosed globally.","PeriodicalId":93288,"journal":{"name":"General medicine and clinical practice","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"General medicine and clinical practice","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31579/2639-4162/037","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

Schistosomiasis may affect a number of organs within the human body. Schistosomiasis may also be associated with glomerular disease of the kidney in the form of glomerulonephritis and nephrotic syndrome. The association between Schistosomiasis and glomerulopathy may not be well known by a number of practitioners and its pathophysiology may not be very well understood and this could be due to the underdiagnosis of the disease due to the possibility of lack of facilities within the Schistosomiasis endemic areas of the world especially within tropical Africa. Nevertheless, there are a number of patterns of renal involvement in Schistosomiasis which include (a) upper urinary tract sequelae of lower urinary tract Schistosomiasis pathology, (b) immune-related glomerulonephritis, (c) as well as oxidant-stress-mediated renal tubular glomerulonephritis. The renal involvement by Schistosomiasis does tend to be ensued by the development of Schistosomiasis-associated Glomerulopathy (Glomerulonephritis / Nephrotic Syndrome) of varying severity. Individuals affected by Schistosomiasis-associated kidney disease may develop (a) asymptomatic disease which tends to related to self-limited and asymptomatic glomerular disease (b) symptomatic disease which most commonly would tend to present with nephrotic syndrome most often in patients who develop hepato-splenic schistosomiasis with liver fibrosis associated with Schistosoma mansoni infection. Symptomatic patients tend to develop severe hypo-proteinemia, half of the patients tend to have elevated blood pressure. In the absence of nephrotic syndrome, patients who have Schistosomiasis-associated glomerulopathy may manifest with: (a) isolated non-nephrotic syndrome proteinuria (b) acute glomerulonephritis associated with haematuria and heavy proteinuria, (c) Nephrotic syndrome together with systemic manifestations of co-infection with salmonella (class II) or hepatitis C virus (Class I), (d) End stage renal disease (ESRD). Some of the patients who have Schistosomiasis of the kidney may present with Haematuria, Hypertension, Hepato-splenic Schistosomiasis. The diagnosis should be suspected with regard to the following scenarios: (a) clinical suspicion in a patient with kidney disease who is known or has been known to have Schistosoma mansoni; (b) exposure to an endemic area, (c) clinical evidence / demonstration of chronic hepatosplenic schistosomiasis, (d) if the patient has not been diagnosed as having been afflicted with schistosomiasis, then schistosomal infection should be documented, (e) majority of patients with schistosomiasis and kidney disease should have kidney biopsy. (f) The patients should be evaluated for co-infection with salmonella, hepatitis C virus, and hepatitis B virus in order to ensure adequate treatment of the disease. Schistosomiasis is the second most devastating tropical parasitic disease globally which tends to be responsible for many urological complications. Nevertheless, glomerular injury is an uncommon complication which has mainly or most often described with Schistosoma Mansoni. When patients who have Schistosomiasis-associated Kidney disease are managed and followed-up on long-term basis with renal end points, one third of the patients independent of the histopathology examination features of the kidney biopsies would tend to progress dialysis. Membranoproliferative glomerulonephritis (MPGN) is an uncommon complication associated with Schistosoma Haematobium infection which tends to be associated with potentially poor prognosis. MPGN could lead quickly to End Stage Renal Disease (ESRD). Anti-helminthic and immunosuppressive medicaments tend not to be effective at advanced stages of the disease and hence efforts need to be focused upon the prevention, early detection, as well as treatment of Schistosoma infections among at-risk groups of individuals. In order to reduce morbidity related to Schistosoma-associated nephropathy, public health policy, should be concentrated upon the prevention of the disease by the control of snail, improved sanitation, and health education, as well as by the implementation, and sustenance of chemotherapy-based control strategies. Considering that many individuals are found yearly to be inflicted by Schistosomiasis who tend to dwell in more rural parts of their countries where facilities for the undertaking of renal function tests and biopsies of the kidney tend not to be readily available, there is the likelihood that Schistosomiasis-associated nephropathies may be highly underdiagnosed globally.
血吸虫病相关肾小球疾病(肾小球肾炎/肾病综合征):文献综述和更新
血吸虫病可能影响人体内的许多器官。血吸虫病也可能与肾小球疾病有关,表现为肾小球肾炎和肾病综合征。血吸虫病和肾小球病之间的联系可能不为许多从业者所熟知,其病理生理学也可能不被很好地理解,这可能是由于在世界血吸虫病流行地区,特别是在热带非洲,可能缺乏设施而导致对该病的诊断不足。然而,血吸虫病的肾脏受累有多种模式,包括(a)下尿路血吸虫病病理的上尿路后遗症,(b)免疫相关的肾小球肾炎,(c)以及氧化应激介导的肾小管肾小球肾炎。血吸虫病对肾脏的损害往往伴随着不同程度的血吸虫病相关肾小球病(肾小球肾炎/肾病综合征)的发展。受血吸虫病相关肾脏疾病影响的个体可能会出现(a)无症状疾病,这往往与自限性和无症状肾小球疾病有关;(b)有症状疾病,最常见的是肾病综合征,最常见于肝脾血吸虫病患者,并伴有与曼氏血吸虫感染相关的肝纤维化。有症状的患者往往发展为严重的低蛋白血症,一半的患者往往血压升高。在没有肾病综合征的情况下,血吸虫病相关肾小球病变患者可能表现为:(a)孤立性非肾病综合征蛋白尿(b)伴有血尿和重度蛋白尿的急性肾小球肾炎,(c)肾病综合征并伴有沙门氏菌(II类)或丙型肝炎病毒(I类)感染的全身性表现,(d)终末期肾病(ESRD)。有些肾脏血吸虫病患者可能会出现血尿、高血压、肝脾血吸虫病。应根据以下情况怀疑诊断:(a)临床怀疑患有肾脏疾病的患者,已知或已知患有曼氏血吸虫;(b)暴露于流行地区,(c)慢性肝脾血吸虫病的临床证据/证明,(d)如果患者未被诊断为患有血吸虫病,则应记录血吸虫感染,(e)大多数血吸虫病和肾脏疾病患者应进行肾脏活检。(f)应评估患者是否同时感染沙门氏菌、丙型肝炎病毒和乙型肝炎病毒,以确保对该疾病进行适当治疗。血吸虫病是全球第二大破坏性热带寄生虫病,往往会导致许多泌尿系统并发症。然而,肾小球损伤是一种罕见的并发症,主要或最常被描述为曼森血吸虫。当对血吸虫病相关肾病患者进行管理和长期肾终点随访时,三分之一独立于肾活检组织病理学检查特征的患者倾向于进行透析。膜增生性肾小球肾炎(MPGN)是一种罕见的与血血吸虫感染相关的并发症,往往与潜在的不良预后有关。MPGN可迅速导致终末期肾病(ESRD)。抗蠕虫和免疫抑制药物在疾病晚期往往无效,因此需要将工作重点放在高危人群中血吸虫感染的预防、早期发现和治疗上。为了降低血吸虫相关肾病的发病率,公共卫生政策应侧重于通过控制蜗牛、改善卫生条件和健康教育以及实施和维持以化疗为基础的控制策略来预防该病。考虑到每年都有许多人被发现患有血吸虫病,这些人往往居住在其国家的农村地区,在那里进行肾功能检查和肾脏活检的设施往往不容易获得,因此,在全球范围内,与血吸虫病相关的肾病可能高度未得到诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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