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Surgical management of cystic dilatation bile ducts in adults

机译:成人囊性扩张胆管的外科治疗

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BACKGROUND: The cystic dilatation of the biliary tract is a rare disease and uncertain origin. It is recognized more frequently in children; however, its incidence comes increasing in adults, representing 20% of the cases. AIM: To evaluate morbimortality rates, evolution and handing of patients with cystic dilatation bile ducts in adults. METHODS: Were evaluated, retrospectively, five adults who had the diagnosis of choledochal cyst and that had been submitted to some surgical procedure. RESULTS: Abdominal pain was the commonest complain to all patients. Jaundice was present in 80%. Ultrasound scanning was done in all the cases as initial examination. CT scan, magnetic resonance imaging and endoscopic retrograde cholangiopancreatography were also done in some patients; however, the diagnosis was established intra-operatively in all cases. The cyst resection with reconstruction of the biliary tract was done in 60%; the cystojejunostomy in 20%; and in 20% biliary tract drainage. CONCLUSIONS: Biliary tract cystic dilatation is a rare disease. However, its incidence is increasing in the adult population, so, it must be thought as differential diagnosis when facing obstructive jaundice.
机译:背景:胆道的囊性扩张是一种罕见的疾病和不确定的来源。它在儿童中更频繁地认识到;然而,其发病率在成年人中越来越多,占该病例的20%。目的:评价成人中囊性扩张胆管患者的病症率,进化和递给患者。方法:评估,回顾性,有五个成年人诊断Choledochal囊肿并提交给一些外科手术。结果:腹痛是所有患者的最常见的抱怨。黄疸有80%。超声扫描在所有情况下都完成了初始检查。 CT扫描,磁共振成像和内窥镜逆行胆管胆痴呆症也在一些患者中进行;然而,在所有情况下,诊断是可操作的。重建胆道的囊肿切除在60%; Cystojejunostomy 20%;在20%的胆道引流中。结论:胆道囊性扩张是一种罕见的疾病。然而,它的发病率在成年人群中越来越多,因此,在面向阻塞性黄疸时,它必须被认为是差异诊断。

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