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[肝外胆管孤立性先天性狭窄]

[Isolated congenital stenoses of the extrahepatic bile ducts].

作者信息

Vázquez Rueda F, Paredes Esteban R M, Escassi Gil A, Olias Gutierrez-Barea J J, Ocaña Losa J M

机构信息

Servicio de Cirugía Pediátrica, Hospital Universitario Reina Sofía, Córdoba.

出版信息

Cir Pediatr. 1993 Jan;6(1):40-3.

PMID:8499237
Abstract

Congenital isolated strictures of the extrahepatic bile ducts are very rare, with only eleven cases reported until 1990. We report two infants (3 and 2 months old, respectively) one of them with a choledocal stenosis and the other with a congenital stricture of the common hepatic duct and spontaneous perforation of the biliary tract. Dilatation of the distal stricture with insertion of T-tube was performed during surgical act. We get success with this technique in both cases.

摘要

先天性肝外胆管孤立性狭窄非常罕见,截至1990年仅有11例报道。我们报告了两名婴儿(分别为3个月和2个月大),其中一名患有胆总管狭窄,另一名患有肝总管先天性狭窄并伴有胆道自发性穿孔。手术过程中对远端狭窄进行了扩张并置入T管。我们在这两例中均成功应用了该技术。

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