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首页> 外文期刊>Medicine. >Asymptomatic sinusitis as an origin of infection-related glomerulonephritis manifesting steroid-resistant nephrotic syndrome: A case report
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Asymptomatic sinusitis as an origin of infection-related glomerulonephritis manifesting steroid-resistant nephrotic syndrome: A case report

机译:无症状鼻窦炎作为感染相关的肾小球肾炎的起源,表现出类固醇抗性肾病综合征:案例报告

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Rationale: Infection is a major trigger or pathogenic origin in a substantial proportion of glomerulonephritis (GN) patients, typically manifesting infection-related GN (IRGN). Various microorganisms, infection sites, and clinical and histopathological features are involved in IRGN. Once an infectious origin is identified and successfully eradicated, nephrotic syndrome or kidney dysfunction is spontaneously resolved. However, if patients are asymptomatic and the origin is undetermined, the diagnosis and treatment of GN is challenging. This case presentation reported on an IRGN case manifesting steroid-resistant nephrotic syndrome associated with asymptomatic sinusitis as a pathogenic origin. Patient concerns: A 68-year-old male presented with severe kidney dysfunction and edema in both extremities. Diagnosis: The patient was clinically diagnosed with hypocomplementemic nephrotic syndrome and kidney dysfunction and histopathologically with diffuse proliferative GN and a focal pattern of membranoproliferative GN. The findings suggested that idiopathic membranoproliferative glomerulonephritis type I was more likely than IRGN, given a critical lack of apparent infection. Interventions: Combined intravenous methylprednisolone, oral prednisolone, and cyclosporin did not improve the patient's condition. Thus, IRGN associated with inapparent infectious origin was suspected. Repeated thorough and careful examinations including CT scan showed sinusitis in his left maxillary sinus. Moreover, reanalysis of kidney specimen revealed positive nephritis-associated plasmin receptor in glomeruli, a typical finding for IRGN, supporting a pathogenic significance of his sinusitis . Medical treatment was initiated with 200 mg oral clarithromycin daily. Outcomes: Oral clarithromycin gradually improved proteinuria and hypocomplementemia and resulted in nephrotic syndrome remission in parallel with opacification resolution of sinuses shown on CT. Lessons: This case presentation showed that asymptomatic sinusitis is potentially a pathogenic IRGN origin. A gold standard therapy for idiopathic GN, corticosteroid could be damaging in uncontrolled or underdiagnosed infection. In asymptomatic patients, a thorough screening of infectious diseases, including sinusitis , together with a renal histological evaluation of glomerular nephritis-associated plasmin receptor deposition is also essential in treating a wide spectrum of GN.
机译:理由:感染是主要触发或致病原因,其肾小球肾炎(GN)患者通常表现出感染相关的GN(IRGN)。各种微生物,感染部位和临床和组织病理学特征参与IRGN。一旦鉴定出现传染性且成功消除,肾病综合征或肾功能障碍被自发地解决。但是,如果患者无症状,原产地未确定,GN的诊断和治疗是具有挑战性的。本病例介绍报告了在IRGN案例中表现出与无症状鼻窦炎相关的类固醇抗性肾病,作为病原起源。患者担忧:68岁男性在两端患有严重的肾功能障碍和水肿。诊断:患者在临床上被诊断诊断患有低微血症肾病综合征和肾功能紊乱,并且具有弥漫性增殖性GN的组织病理学和膜升压性GN的焦点图。结果表明,鉴于显体感染缺乏危急缺乏表现致力致力膜,肾小球肾炎型I比IRGN更可能。干预:结合静脉内甲基丙酮,口服泼尼松和环孢菌素没有改善患者的病症。因此,怀疑与缺磷感染源相关的IRGN。重复彻底和仔细的检查,包括CT扫描在他左上颌窦中显示出鼻窦炎。此外,肾标本的重新分析显示了肾小球中阳性肾炎相关纤溶酶受体,典型的IRGN发现,支持他鼻窦炎的致病意义。用200毫克口服克拉霉素每天发起医疗。结果:口服克拉霉素逐渐改善蛋白尿和低综合症,导致与CT上显示的鼻窦的透明分辨率平行进行肾病综合征缓解。课程:这种情况表明,无症状鼻窦炎是可能是致病IRGN起源。对特性GN的黄金标准疗法,皮质类固醇可能因不受控制或未诊断的感染而损害。在无症状患者中,彻底筛查包括鼻窦炎,包括肾小球肾炎相关纤溶酶受体沉积的肾组织学评估,对治疗广谱的GN也必不可少。

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