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首页> 外文期刊>Scandinavian journal of gastroenterology. >Membranous Budd-Chiari syndrome in Caucasians.
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Membranous Budd-Chiari syndrome in Caucasians.

机译:白人的膜性Budd-Chiari综合征。

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摘要

OBJECTIVE: Budd-Chiari syndrome (BCS) is characterized by an obstruction of hepatic venous outflow. Membranous obstruction of the inferior vena cava (IVC) is a curable cause of primary BCS but is very rare in Western Europe. To date, there is only very limited information on membranous BCS in the Western world. We here report the diagnosis and management of five Caucasian patients with membranous BCS. MATERIAL AND METHODS: Out of 23 patients with BCS diagnosed between 2004 and 2007 we identified five with a membranous web of the IVC. Diagnostic evaluation of BCS included laboratory tests, ultrasound Doppler imaging, CT and MRI. RESULTS: The clinical presentation of membranous BCS was heterogeneous. The time frame from first clinical symptoms to diagnosis ranged from 3 weeks to 60 years. Liver cirrhosis was misdiagnosed in 4/5 patients. CT did not establish the correct diagnosis of membranous BCS in any of our patients. In contrast, abdominal Doppler ultrasonography showed collaterals and a web in the IVC which was confirmed by Doppler-MRI and hepatovenography. Four patients underwent interventional treatment with balloon dilatation of short-segment venous stenoses or complete occlusions. Therapy was successful: in all cases it resulted in a normalized extrahepatic blood flow and reduction of spleen size. CONCLUSIONS: Membranous BCS may be underdiagnosed in Caucasians. Doppler ultrasound should be used as the initial diagnostic procedure for membranous BCS. Although CT is considered the "gold standard" in addition to angiography, it could not detect membranous obliteration in our cases. Patients can be effectively treated by interventional endovascular therapy.
机译:目的:Budd-Chiari综合征(BCS)的特征是阻塞肝静脉流出。下腔静脉膜性阻塞是可治愈的原发性BCS的病因,但在西欧很少见。迄今为止,在西方世界关于膜状BCS的信息非常有限。我们在这里报告了5例白种人的膜性BCS患者的诊断和治疗。材料与方法:在2004年至2007年之间诊断出的23例BCS患者中,我们确定了5例具有IVC膜状网。 BCS的诊断评估包括实验室检查,超声多普勒成像,CT和MRI。结果:膜状BCS的临床表现是异质的。从最初的临床症状到诊断的时间范围为3周到60年。肝硬化在4/5患者中被误诊。在我们的任何患者中,CT均不能正确诊断膜性BCS。相反,腹部多普勒超声检查显示在IVC中有侧支和腹板,这通过多普勒MRI和肝静脉造影证实。四名患者接受了短段静脉狭窄或完全闭塞的球囊扩张介入治疗。治疗是成功的:在所有情况下,它均使肝外血流正常化并减少了脾脏的大小。结论:高加索人膜状BCS可能被误诊。多普勒超声应作为膜性BCS的初始诊断程序。尽管CT被认为是血管造影之外的“黄金标准”,但在我们的病例中它无法检测到膜性闭塞。介入性血管内治疗可以有效地治疗患者。

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