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首页> 外文期刊>American Journal of Case Reports >Anti-Glomerular Basement Membrane Disease Combined with IgA Nephropathy Complicated with Reversible Posterior Leukoencephalopathy Syndrome: An Unusual Case
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Anti-Glomerular Basement Membrane Disease Combined with IgA Nephropathy Complicated with Reversible Posterior Leukoencephalopathy Syndrome: An Unusual Case

机译:抗肾小球基底膜病合并IgA肾病并发可逆性后脑白质脑病综合征:不寻常的情况

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Patient: Male, 24 Final Diagnosis: Crescentic glomerulonephritis (type I) with IgA nephropathy Symptoms: Headache ? gross hematuria ? nocturia ? seizures Medication: Cyclophosphamide Clinical Procedure: Dignosis to treatment Specialty: Nephrology Objective: Rare co-existance of disease or pathology Background: Anti-glomerular basement membrane disease (anti-GBM disease) is an autoimmune glomerulonephritis disease that is characterized by IgG linear deposition along the non-collagen domain of α3 chains of type IV collagen on the GBM. Although anti-GBM disease accompanied with IgA linear deposition along GBMs was discussed previously in some papers, anti-GBM disease combined with IgA granular deposition in the mesangial area, especially complicated with reversible posterior leukoencephalopathy syndrome (RPLS), was rarely reported. RPLS is usually caused by hypertensive encephalopathy, renal decompensation, fluid retention, and adverse effects of immunosuppressive drugs. Case Report: A male patient with the chief complaints of headache, gross hematuria, and nocturia was referred to our hospital. Based on renal biopsy, the diagnosis was finally confirmed as anti-GBM disease combined with IgA nephropathy and, the patient received comprehensive treatment, including cyclophosphamide (CTX), which led to symptom improvement. Two days after the third impulse CTX was given, he suddenly experienced headache and dizziness, which eventually developed into a tonic-clonic seizure. RPLS was identified by cranial magnetic resonance imaging (MRI) with reversible neuroimaging. After diazepam and antihypertension management, seizures were controlled. RPLS, a neurological complication, was found in anti-GBM disease with IgA nephropathy during our immunosuppressants therapy for the first time. Conclusions: It is worth paying more attention to patients with rapidly progressive glomerulonephritis (RPGN), as they might be complicated with RPLS during intravenous administration of CTX and methylprednisolone. We suggest the neuroimaging be examined as soon as the seizure happens.
机译:患者:男性,24岁最终诊断:患有IgA肾病的新月型肾小球肾炎(I型)症状:头痛?肉眼血尿?夜尿症?癫痫发作药物:环磷酰胺临床程序:木乃伊病治疗专长:肾脏病目的:罕见疾病或病理共存背景:抗肾小球基底膜疾病(抗GBM疾病)是一种自身免疫性肾小球肾炎,其特征是沿IgG线性沉积GBM上IV型胶原的α3链的非胶原结构域。尽管先前在一些论文中讨论了抗GBM疾病伴随IgA沿GBMs线性沉积的现象,但很少报道抗GBM疾病结合IgA颗粒沉积在系膜区,尤其是并发可逆性后脑白质脑病综合征(RPLS)。 RPLS通常是由高血压性脑病,肾脏代偿失调,体液retention留和免疫抑制药物的不良反应引起的。病例报告:男性患者主诉头痛,严重血尿和夜尿症,已转诊至我院。根据肾脏活检,诊断最终被确认为抗GBM疾病合并IgA肾病,患者接受了包括环磷酰胺(CTX)在内的综合治疗,从而改善了症状。在给予第三次脉冲CTX的两天后,他突然感到头痛和头晕,最终发展为强直性阵挛性癫痫发作。 RPLS通过颅骨磁共振成像(MRI)和可逆神经影像识别。经过地西epa和抗高血压治疗,癫痫发作得到控制。 RPLS是一种神经系统并发症,在我们的免疫抑制剂治疗期间首次在具有IgA肾病的抗GBM疾病中发现。结论:值得迅速关注快速进展性肾小球肾炎(RPGN)的患者,因为在静脉内给予CTX和甲基强的松龙的过程中可能会合并RPLS。我们建议在癫痫发作后立即检查神经影像。

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