Hepatic resection in localized Caroli disease

Ricardo Espinoza G, Sergio San Martin R, Felipe Court A, Emilio Vera P, Rodrigo Ferreira S, Héctor Croxatto A

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Caroli disease is a cystic congenital malformation of the intrahepatic biliary tract, frequently associated with lithiasis. Commonly, cystic dilatations are bilateral and infrequently they affect only one hepatic lobule or segment. We report six patients with localized Caroli disease, three in the right and three in the left hepatic lobule, that were subjected to a hepatic resection. There were no postoperative complications or mortality. After 28 months of follow up, patients are asymptomatic and with normal hepatic function and ultrasonography. The importance of diagnosing localized Caroli disease, in which hepatic resection can be curative, is emphasized.
Original languageAmerican English
Pages (from-to)183-189
Number of pages7
JournalRevista Medica de Chile
Volume131
Issue number2
StatePublished - 1 Feb 2003

Keywords

  • Caroli disease
  • Hepatectomy
  • Lithiasis

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