首页> 美国卫生研究院文献>The International Journal of Angiology : Official Publication of the International College of Angiology Inc >Renosplenic Shunting in the Nutcracker Phenomenon: A Discussion and Paradigm Shift in Options? A Novel Approach to Treating Nutcracker Syndrome
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Renosplenic Shunting in the Nutcracker Phenomenon: A Discussion and Paradigm Shift in Options? A Novel Approach to Treating Nutcracker Syndrome

机译:胡桃夹子现象中的肾脾分流:选择的讨论和范式转变?一种治疗胡桃夹综合征的新方法

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摘要

The nutcracker syndrome is a rare clinical manifestation of symptoms caused by the compression of the left renal vein by an overriding superior mesenteric artery, an anatomical variant otherwise known as the nutcracker phenomenon. Usually present in women and children, when symptomatic, it commonly presents with hematuria, proteinuria, and chronic pelvic pain. Effective modalities of treatment apart from conservative management, include both invasive surgical procedures such as renal vein transposition and autotransplantation of the kidney and more popular recently, the less invasive endovascular stenting. Both options, however, are not without complications, such as, retroperitoneal hematomas or stent migration, thrombosis and restenosis. We now present a case of spontaneous renosplenic shunting in a 68-year-old lady of Chinese descent with the nutcracker syndrome—the first of such cases to be ever reported in a patient with no preexisting predilection for chronic liver disease and portosystemic shunting. Despite having significant pelvic venous congestion as evident on computed tomography scans, she remained asymptomatic. This may present a novel paradigm shift for the treatment of the nutcracker syndrome —surgical creation of a renosplenic bypass instead of current modalities, an alternative solution which can be performed laparoscopically and is without problems related to stent use. The creation of laparoscopic splenorenal bypass has been reported once thus far in Cleveland Ohio by Chung and Gill with good symptomatic improvement but no further studies since to validate its long-term effectiveness.
机译:胡桃夹子综合症是一种罕见的临床症状,该症状是由高位肠系膜上动脉压迫左肾静脉引起的,这种解剖学变异也称为胡桃夹子现象。通常在妇女和儿童中出现症状时,通常表现为血尿,蛋白尿和慢性盆腔痛。除保守治疗外,有效的治疗方式包括侵入性外科手术,例如肾静脉移位和肾脏自体移植,近来更流行,侵入性较小的血管内支架置入术。然而,这两种选择都并非没有并发症,例如腹膜后血肿或支架迁移,血栓形成和再狭窄。现在,我们介​​绍了一名因胡桃夹子综合征而后裔的68岁中国血统患者的自发性鼻气管分流术,这是有史以来首例针对慢性肝病和门体系统分流不存在偏爱的患者。尽管计算机断层扫描显示骨盆静脉明显充血,但她仍无症状。这可能会提出一种新的方式来治疗胡桃夹子综合征-外科手术创建鼻窦旁路术,而不是目前的方式,这是一种可以腹腔镜进行的替代解决方案,并且没有与支架使用相关的问题。到目前为止,Chung和Gill曾在俄亥俄州的克利夫兰报道过腹腔镜脾肾旁路手术的建立,其症状改善良好,但自从证实其长期有效性以来没有进一步的研究。

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