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Childhood Nephrotic Syndrome Complicated by Catastrophic Multiple Arterial Thrombosis Requiring Bilateral Above-Knee Amputation

机译:儿童肾病综合征复杂的灾难性多动脉血栓形成,需要双边膝关节截肢

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摘要

Background: Thromboembolic events are rare but critical complications in childhood nephrotic syndrome. The veins are more commonly affected, while arterial thrombosis is extremely rare but often life-threatening. Herein, we describe the clinical course of a 10-years-old girl with catastrophic multiple arterial thrombosis at the primary onset of nephrotic syndrome who underwent bilateral above-knee amputation.Case diagnosis/treatment: A previous healthy 10-years-old girl contracted the influenza B virus. Five days later, she suddenly developed severe ischemia in both legs. Physical examination showed eyelid and leg edema, and laboratory tests revealed hypoalbuminemia and acute kidney injury. After undergoing contrast-enhanced computed tomography, the patient was diagnosed with multiple arterial thrombosis (including the bilateral iliac arteries) due to nephrotic syndrome. Despite the performance of surgical thrombectomies, fasciotomy, and systematic heparinization, she required bilateral above-knee amputation. The patient achieved spontaneous remission of nephrotic syndrome, and her renal function fully recovered. There were no findings suggestive of secondary nephrotic syndrome and antiphospholipid syndrome. Her protein C and protein S concentrations were slightly decreased at admission. However, whole-exome sequencing revealed a thrombotic risk variant (T630I) in the PROS1 gene encoding protein S. This missense variant is often reported in patients with thrombosis or protein S deficiency, and may result in a thrombotic predisposition in some situations, such as nephrotic syndrome.Conclusions: Arterial thrombosis is a rare complication; however, it must be considered, especially in patients with new-onset nephrotic syndrome. Early recognition is important for early intervention and prevention of serious sequelae.
机译:背景:血栓栓塞事件是儿童肾病综合征的罕见但关键并发症。静脉更常见,而动脉血栓形成极少,但往往危及生命。在此,我们描述了一个10岁女孩的临床过程,在膝关节综合征的肾病综合征的主要发病中遭受灾难性的多动脉血栓形成。诊断/治疗,诊断/治疗:一个以前的健康10岁的女孩收缩流感B病毒。五天后,她突然在两条腿上发育严重的缺血。体检显示眼睑和腿部水肿,实验室测试显示出低钠血症和急性肾损伤。经过对比增强的计算断层扫描后,由于肾病综合征,患者被诊断出患有多个动脉血栓形成(包括双侧髂动脉)。尽管表现了外科血液切除术,诱饵和系统的肝素,但她需要双侧膝关节截肢。患者达到了肾病综合征的自发缓解,她的肾功能完全恢复。没有发现次肾综合征和抗磷脂综合征的发现。在入院时,她的蛋白C和蛋白质浓度略微降低。然而,全外序列揭示了PROF1基因编码蛋白S中的血栓性风险变体(T630I)。血栓形成或蛋白质缺乏的患者通常报道该畸形变体,并且可能导致某些情况下的血栓形成易感性,例如肾病综合征。结论:动脉血栓形成是一种罕见的并发症;然而,必须考虑,特别是在患有新发病肾病综合征的患者中。早期识别对于早期干预和预防严重后遗症是重要的。

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