Cysta choledochu napodobující pseudocystu pankreatu - kazuistika 39 letého muže

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00843989%3A_____%2F07%3A00014595" target="_blank" >RIV/00843989:_____/07:00014595 - isvavai.cz</a>

Výsledek na webu

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DOI - Digital Object Identifier

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Jazyk výsledku

angličtina

Název v původním jazyce

A Case Report of a 39-year-old Male with Choledochal Cyst Mimicking Pancreatic Pseudocyst

Popis výsledku v původním jazyce

In European countries, choledochal cysts are rare anomalies of the bile tract. At the Surgery Department of the University Hospital Ostrava, a case of a patient with cystic lesion of the pancreatic head was solved. According to ultrasonography and computer tomography it was assumed to be a pancreatic pseudocyst. Only after a complete additional examination of the pancreatico-biliary system, was it diagnosed la-type cystic dilatation of the common bile duct, accompanied by stenosis in its terminal part.With regard to the age of the first clinical symptoms, their character and histopathological findings, congenital origin is assumed in both of these anomalies. After provisional percutaneous transhepatic biliary drainage, a duodenohemipancreatectomy wasperformed with complete cyst excision. Until now, nine months later, the patient has shown absolutely no clinical difficulties.

Název v anglickém jazyce

A Case Report of a 39-year-old Male with Choledochal Cyst Mimicking Pancreatic Pseudocyst

Popis výsledku anglicky

In European countries, choledochal cysts are rare anomalies of the bile tract. At the Surgery Department of the University Hospital Ostrava, a case of a patient with cystic lesion of the pancreatic head was solved. According to ultrasonography and computer tomography it was assumed to be a pancreatic pseudocyst. Only after a complete additional examination of the pancreatico-biliary system, was it diagnosed la-type cystic dilatation of the common bile duct, accompanied by stenosis in its terminal part.With regard to the age of the first clinical symptoms, their character and histopathological findings, congenital origin is assumed in both of these anomalies. After provisional percutaneous transhepatic biliary drainage, a duodenohemipancreatectomy wasperformed with complete cyst excision. Until now, nine months later, the patient has shown absolutely no clinical difficulties.

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

FJ - Chirurgie včetně transplantologie

OECD FORD obor

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Projekt

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Návaznosti

V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Rok uplatnění

2007

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Hepato-Gastroenterology

ISSN

0172-6390

e-ISSN

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Svazek periodika

54

Číslo periodika v rámci svazku

74

Stát vydavatele periodika

GR - Řecká republika

Počet stran výsledku

4

Strana od-do

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Kód UT WoS článku

000246271800017

EID výsledku v databázi Scopus

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