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与青紫型先天性心脏病相关的肝外胆道闭锁。三例病例报告及文献综述。

Extrahepatic biliary atresia associated with cyanotic congenital heart disease. Three case reports and a review.

作者信息

Zukin D D, Liberthson R R, Lake A M

出版信息

Clin Pediatr (Phila). 1981 Jan;20(1):64-6. doi: 10.1177/000992288102000110.

Abstract

Three patients with extrahepatic biliary atresia associated with cyanotic congenital heart disease are presented and their clinical courses reviewed. In these patients, the coincidence of cyanosis and jaundice caused an atypical green-appearing cutaneous discoloration which masked the early clinical detection of biliary atresia in one infant and cyanotic heart disease in the other two. In all infants, either partial or complete correction of the congenital cardiac lesion was possible. Two infants died from hepatic disease despite attempted surgical revision and one has satisfactory bile drainage one month following portoenterostomy. Awareness of the rare concurrence of cyanotic congenital heart disease and extrahepatic biliary atresia is helpful to the clinician when evaluating infants with atypical cutaneous discoloration. Early oversight of either underlying disease process can be avoided, and early evaluation and management of both entities can be possible.

摘要

本文报告了3例合并紫绀型先天性心脏病的肝外胆道闭锁患者,并回顾了他们的临床病程。在这些患者中,紫绀和黄疸同时出现导致皮肤出现非典型的绿色变色,这掩盖了1例婴儿早期临床诊断的胆道闭锁以及另外2例婴儿的紫绀型心脏病。在所有婴儿中,先天性心脏病变均有可能进行部分或完全矫正。尽管尝试了手术矫正,但仍有2例婴儿死于肝脏疾病,1例在门肠吻合术后1个月胆汁引流情况良好。当评估有非典型皮肤变色的婴儿时,认识到紫绀型先天性心脏病和肝外胆道闭锁的罕见并发情况对临床医生很有帮助。可以避免对任何一种潜在疾病过程的早期忽视,并且可以对这两种疾病进行早期评估和管理。

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