1996
DOI: 10.1002/(sici)1097-0223(199610)16:10<934::aid-pd961>3.0.co;2-4
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Early Prenatal Diagnosis of Choledochal Cyst

Abstract: Unrecognized biliary tract obstruction due to choledochal cysts or biliary atresia can result in significant morbidity and mortality. Diagnosis in utero of choledochal cyst allows prompt postnatal diagnostic evaluation and appropriate surgical therapy to be instituted early in life. This may minimize the potential complications of cholangitis, cirrhosis, and liver failure in infants with choledochal cysts.

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Cited by 14 publications
(5 citation statements)
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“…The occurrence of choledochal cysts in twins [41], in siblings, and their detection in utero [42,43] supports that, at least in some children, a genetic abnormality [44][45][46] leads to a developmental abnormality including biliary papillomatosis [47,48], leading to cyst formation in the developing fetus. The occurrence of choledochal cysts in twins [41], in siblings, and their detection in utero [42,43] supports that, at least in some children, a genetic abnormality [44][45][46] leads to a developmental abnormality including biliary papillomatosis [47,48], leading to cyst formation in the developing fetus.…”
Section: Pathophysiologymentioning
confidence: 99%
“…The occurrence of choledochal cysts in twins [41], in siblings, and their detection in utero [42,43] supports that, at least in some children, a genetic abnormality [44][45][46] leads to a developmental abnormality including biliary papillomatosis [47,48], leading to cyst formation in the developing fetus. The occurrence of choledochal cysts in twins [41], in siblings, and their detection in utero [42,43] supports that, at least in some children, a genetic abnormality [44][45][46] leads to a developmental abnormality including biliary papillomatosis [47,48], leading to cyst formation in the developing fetus.…”
Section: Pathophysiologymentioning
confidence: 99%
“…Choledochal cysts are rarely encountered, occurring more frequently in Asian populations 2,24 . Sonographically, they usually present as a cyst in the right upper quadrant in the region of the porta hepatis, separate from the gallbladder and duodenum 2,24 . The diagnosis can be definitively made when bile ducts are seen in continuity with the cyst 1,24 .…”
Section: Rare Causes Of Foetal Abdominal Cystic Massesmentioning
confidence: 99%
“…(Fig. 14) A choledochal cyst might be identified in the early second ­trimester 24 . The differential diagnosis of an upper abdominal cyst includes duplication cyst, congenital hepatic cyst, gallbladder duplication, the distended duodenum of duodenal atresia and situs inversus, in which case the ‘cyst’ represents the abnormally sited stomach 2,3…”
Section: Rare Causes Of Foetal Abdominal Cystic Massesmentioning
confidence: 99%
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“…In the prenatal US, fetal CDCs have been described as follows: anechoic cysts located in the right upper quadrant of the abdomen, the subhepatic, or the region of the porta hepatis, with no septum, and these are connected to the gallbladder or hepatic ducts [ 7 ]. The latter two have always been considered as decisive signs in the prenatal diagnosis [ 8 ], but these could not be observed in all prenatal CDC cases [ 9 ], and the accuracy for the prenatal diagnosis of CDCs is only 7.7% [ 10 ]. Fetal CDCs may be misdiagnosed as origin-uncertain abdominal cysts, duodenal atresia, hepatic cysts, ovarian cysts, mesenteric cysts, renal abnormalities, normal gallbladder, or situs inversus [ 11 ].…”
Section: Introductionmentioning
confidence: 99%