Rebollar GRC, García ÁJ, Santamaría AJR, Dávila RD, Hernández CD, Gómez VH

Language: Spanish
References: 0
Page: 103-106
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ABSTRACT

The choledocal chyst are arare entity that present with a clinical manifestation insidious and more frequent in child, instead the diagnosis can be made late in adult 1ife. It is more frequent in women in the relation of 3:1. The origin of these dilatations hasn't been established postulatingthe acquired and the congenital. The typical clinical presentation is with pain, jaundice and palpable mass in the abdomen, but th is triad is uncommon. The treatment of choice in the chyst type I is the chystectomy with hepatoyeyunoanastomosis in Y of Roux.