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- Ultrastructural study on myocardial tissue in a case of congenital biliary atresia 先天性胆道闭锁患儿心肌组织的电镜观察
- Ultrastructure of intrahepatic biliary canaliculi and prognosis of congenital biliary atresia 先天性胆道闭锁肝内毛细胆管超微结构与临床预后关系探讨
- congenital biliary atresia 先天性胆道闭锁
- When I was born, I was diagnosed with a disease called biliary atresia. 我出生时被诊断患有一种叫胆道闭锁的疾病。
- Objective To reduce the complication of congenital biliary diliation(CBD),and improve the cure rate of CBD. 目的探讨先天性胆管扩张症并发症的预防和处理,提高治愈率。
- This 3 month old child died with extrahepatic biliary atresia, a disease in which there is inflammation with stricture of hepatic or common bile ducts. 肝外胆道闭锁为肝脏或胆总管的狭窄与炎症，这是一例死于肝外胆道闭锁的3个月婴儿。
- The pathology of liver was studied in 14 patients with congenial biliary atresia after Kasai's operation. 对14例胆道闭锁患儿进行葛西手术后肝脏病理变化的研究。
- Biliary atresia is a common, cholestatic disease of infancy of unknown cause with a poor prognosis. 胆道闭锁(Biliary atresia,BA)是新生儿胆汁郁积最常见的原因，病因尚不明确，预后差。
- Conclusion Cyst excision with button loop hepaticojejunostomy is recommended as the treatment of choice for patients with congenital biliary duct cyst.This procedure is kindred... 结论本术式的优点是不切断空肠及其系膜,能简化手术操作,缩短手术时间,减少对病人的手术打击,适用于任何年龄组行择期手术的本症病人。
- Methods Among 97 biliary atresia patients undergoing Kasai or Suruga operation from Mar 1989 to Mar 1999, 35 cases have survived over five years. 方法 总结1989年3月至1999年3月行Kasai手术及其改良术式Suruga手术治疗胆道闭锁的疗效。
- Objective: The aim of this study is to establish the diagnosis and evaluate the prognosis of extrahepatic biliary atresia with histopathology. 目的：通过病理学方法，作出肝外胆道闭锁的诊断和预后判定。
- Objective To study the prognostic value of perioperative portal pressure at time of Kasai operation in patients with biliary atresia (BA). 结果术中门脉压力正常患儿带自体肝5年和10年生存率较门静脉压力升高组显著延长。
- Abstract Objective: The aim of this study is to establish the diagnosis and evaluate the prognosis of extrahepatic biliary atresia with histopathology. 摘要目的：通过病理学方法，作出肝外胆道闭锁的诊断和预后判定。
- Biliary atresia is a birth defect in which the bile ducts do not have normal openings, preventing bile from leaving the liver. 胆道闭锁是一种不正常发育，使得胆管不能正常打开，导致胆汁不能离开肝脏产生作用。
- For diagnosing biliary atresia, the specificity and accuracy of scintigraphy were 100% and 89.1%, for diagnosing infantile hepatitis syndrome, the sensitivity was 81.7%. 核素肝胆显像对EHBA诊断特异性 10 0%25( 86/86) ;诊断的正确性为 89.;1%25 ( 189/2 12 );对IHS诊断的敏感性为 81
- Abstract: Objective: The aim of this study is to establish the diagnosis and evaluate the prognosis of extrahepatic biliary atresia with histopathology. 文摘:目的：通过病理学方法，作出肝外胆道闭锁的诊断和预后判定。
- Kotb MA,Sheba M,EL Koofy N.Post-portoenterostomy triangular cord sign prognostic value in biliary atresia:a prospective study.Br J Radiol,2005,78(934):884-887. 李桂生;谢永荣;刘钧澄;等.;B超观察肝门纤维块-早期诊断胆道闭锁
- congenital biliary dilatation(CBD) 先天性胆管扩张症
- Microscopically, extrahepatic biliary atresia leads to this appearance in the liver, with numerous brown-green bile plugs, bile duct proliferation (seen at lower center), and extensive fibrosis. 镜下见，肝外胆道闭锁导致肝脏大量黄绿色胆栓、假胆管增生（见于下面的中央）、广泛纤维化。
- Diagnosis and treatment for biliary atresia 胆道闭锁诊治体会
