Altman R P, Abramson S
J Pediatr Surg. 1985 Oct;20(5):529-34. doi: 10.1016/s0022-3468(85)80481-4.
Despite advances and refinements in diagnostic techniques, distinguishing between cholestatic syndromes and extrahepatic biliary atresia is not always possible. Because there are inherent errors in all diagnostic studies including nuclear scanning, ultrasonography, and liver biopsy some infants presumed to have biliary atresia will come to surgery when, in fact, the bile ducts are partially or completely patent. The decision to proceed with a portoenterostomy or to terminate the procedure depends upon the appearance of the liver and histology of the biopsy.
尽管诊断技术有了进步和改进,但区分胆汁淤积综合征和肝外胆道闭锁并不总是可行的。因为包括核扫描、超声检查和肝活检在内的所有诊断研究都存在固有误差,一些被推测患有胆道闭锁的婴儿实际上胆管部分或完全通畅时却接受了手术。决定进行门肠吻合术或终止该手术取决于肝脏的外观和活检的组织学结果。