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婴儿外科性黄疸:除胆道闭锁外

Surgical jaundice in infants: other than biliary atresia.

作者信息

Holland R M, Lilly J R

机构信息

Department of Surgery, Children's Hospital, Denver, CO.

出版信息

Semin Pediatr Surg. 1992 May;1(2):125-9.

PMID:1345478
Abstract

After biliary atresia, the lesions responsible for surgical jaundice in the infant are perforation of the common bile duct, choledochal cyst, bile plug syndrome, and miscellaneous congenital lesions in descending order of frequency. Perforation of the common bile duct commonly presents with an insidious onset of bilious ascites and is best treated by simple peritoneal drainage. Choledochal cyst usually presents later in childhood but presents in infancy if obstruction of the biliary tree is complete or near complete. Excision is the treatment of choice. Any condition leading to alteration in bile composition may cause bile plug syndrome. Spontaneous resolution is the rule: occasionally, intraoperative irrigation is necessary. Most miscellaneous lesions lend themselves to operative correction.

摘要

胆道闭锁后,导致婴儿外科性黄疸的病变依次为胆总管穿孔、胆总管囊肿、胆栓综合征和其他先天性病变,其发生率呈递减顺序。胆总管穿孔通常表现为隐匿性胆汁性腹水,最佳治疗方法是单纯腹腔引流。胆总管囊肿通常在儿童期较晚出现,但如果胆道树完全或近乎完全梗阻,则在婴儿期出现。手术切除是首选治疗方法。任何导致胆汁成分改变的情况都可能引起胆栓综合征。通常可自行缓解:偶尔需要术中冲洗。大多数其他病变适合手术矫正。

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