1997
DOI: 10.1136/jcp.50.7.617
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Solitary cystic dilatation of the intrahepatic bile duct.

Abstract: A 31 year old man was hospitalised with general fatigue and epigastric pain. Abdominalultrasonography, computedtomography, and magnetic resonance imaging showed a cystic lesion in the left lobe ofthe liver. Endoscopic retrograde cholangiopancreatography and percutaneous transhepatic cholangiography revealed a localised dilatation of the intrahepatic bile duct without any obstruction. However, a large mass of mucinous material was noted in the saccular intrahepatic duct and the common bile duct. There was no ev… Show more

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Cited by 4 publications
(3 citation statements)
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“…As far as we know, although there have been previous case reports of SIBC (17,18), including cases of SIBC in infants (13,19), our series of SIBC cases reported this time are more comprehensive and representative, including multiple surgeries after initial misdiagnosis, the occurrence and treatment of surgical complications, the first diagnosis combined with carcinogenesis, and surgical approach adjustment after accidental detection of malignant lesions during surgery, which is the first comprehensive series of cases and comprehensive analysis of SIBC reports so far. Accordingly, we suggest that SIBC should be considered in the differential diagnosis of patients with solitary cystic mass at the hilum.…”
Section: P2 Table 1 General Information Of Patientsmentioning
confidence: 97%
“…As far as we know, although there have been previous case reports of SIBC (17,18), including cases of SIBC in infants (13,19), our series of SIBC cases reported this time are more comprehensive and representative, including multiple surgeries after initial misdiagnosis, the occurrence and treatment of surgical complications, the first diagnosis combined with carcinogenesis, and surgical approach adjustment after accidental detection of malignant lesions during surgery, which is the first comprehensive series of cases and comprehensive analysis of SIBC reports so far. Accordingly, we suggest that SIBC should be considered in the differential diagnosis of patients with solitary cystic mass at the hilum.…”
Section: P2 Table 1 General Information Of Patientsmentioning
confidence: 97%
“…Caroli disease is an autosomal recessive inheritance linked to mutation in PKHD1 gene. It is classified as type V choledochal cyst by the Todani classification [10]. The cystic lesions are depicted as irregular in shape, fusiform, or saccular (Figures 4A).…”
Section: Localized Caroli Disease or Solitary Dilatation Of Intrahepamentioning
confidence: 99%
“…Conventionally, Roux-Y cysto-jejunostomy is the operative treatment of choice for both HC and CIHD. However, it is technically difficult, with major biliary tract disruption [1,2,[11][12][13]. The migration of bacteria from the intestine to the intrahepatic ducts increases the risk of cholangitis [14][15][16][17].…”
Section: Introductionmentioning
confidence: 99%