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胆道闭锁与非心脏性多脾综合征:超声检查及手术考量

Biliary atresia and noncardiac polysplenic syndrome: US and surgical considerations.

作者信息

Abramson S J, Berdon W E, Altman R P, Amodio J B, Levy J

出版信息

Radiology. 1987 May;163(2):377-9. doi: 10.1148/radiology.163.2.3550880.

Abstract

Ten percent of children with biliary atresia have an associated complex of anomalies, including polysplenia, azygous continuation of the inferior vena cava, preduodenal portal vein, hepatic arterial anomalies, and bilaterally bilobed lungs. These abnormalities will not be detected if the preoperative workup is limited to hepatobiliary nuclear scanning. Ultrasonography is important in the preoperative evaluation of patients suspected of having biliary atresia. It is important to identify the associated abnormalities preoperatively because they have an impact on the initial portoenterostomy and may preclude subsequent orthotopic liver transplantation.

摘要

10%的胆道闭锁患儿伴有一系列复杂的异常情况,包括多脾、下腔静脉奇静脉延续、十二指肠前门静脉、肝动脉异常以及双侧肺叶异常。如果术前检查仅限于肝胆核素扫描,这些异常情况将无法被检测到。超声检查在疑似胆道闭锁患者的术前评估中很重要。术前识别相关异常很重要,因为它们会影响初次肝门空肠吻合术,并且可能排除后续的原位肝移植。

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