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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Fuanglada Tongprasert | en_US |
dc.contributor.author | Kuntharee Traisrisilp | en_US |
dc.contributor.author | Theera Tongsong | en_US |
dc.date.accessioned | 2018-09-04T06:12:22Z | - |
dc.date.available | 2018-09-04T06:12:22Z | - |
dc.date.issued | 2012-01-01 | en_US |
dc.identifier.issn | 10970096 | en_US |
dc.identifier.issn | 00912751 | en_US |
dc.identifier.other | 2-s2.0-83255187366 | en_US |
dc.identifier.other | 10.1002/jcu.20856 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=83255187366&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/51959 | - |
dc.description.abstract | Choledochal cyst is one of the intra-abdominal abnormalities of the biliary ducts that present as a cystic mass in the right upper quadrant abdomen. Prenatal diagnosis has been achieved by the demonstration of a connection between a dilated common bile duct and a cystic lesion. In this report, we describe a pregnant woman in whom routine fetal anomaly scan strongly suggested a choledochal cyst at 29 weeks of gestation by demonstrating a round cystic mass in the right upper quadrant of the abdomen, completely separated from the stomach, bowel loops, and gall bladder, and which showed a connection with the dilated common bile duct. © 2011 Wiley Periodicals, Inc. | en_US |
dc.subject | Medicine | en_US |
dc.title | Prenatal diagnosis of choledochal cyst: A case report | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Journal of Clinical Ultrasound | en_US |
article.volume | 40 | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
Appears in Collections: | CMUL: Journal Articles |
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