Choledochal cyst

Česká verze

Authors: J. Zeithaml ¹; V. Třeška ¹; J. Moláček ¹; F. Heidenreich ²
Authors place of work: Chirurgická klinika FN a LF UK v Plzni přednosta: prof. MUDr. V. Třeška, DrSc. ¹; Klinika zobrazovacích metod FN a LF UK v Plzni přednosta: prof. MUDr. B. Kreuzberg, CSc. ²
Published in the journal: Rozhl. Chir., 2015, roč. 94, č. 9, s. 379-382.
Category: Kazuistiky

Summary

Choledochal cyst is a rare disease with a considerably higher incidence found in the Asian population. Although its etiology is not completely known, the disease is believed to be associated with anomalies in the anatomy of the biliary tract. While being a benign unit, it is considered as a precancerosis with the risk of conversion to the biliary tract carcinoma. Radical surgical removal with biliary tract reconstruction is the only curative solution. The authors present the case report of a patient with choledochal cyst type I according to Todani

Key words:
choledochal cyst − classification – diagnosis − treatment

Zdroje

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