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dc.contributor.authorKasemsri Srisupunditen_US
dc.contributor.authorPhitsanu Mahawongen_US
dc.contributor.authorCholaros Charoenratanaen_US
dc.contributor.authorTheera Tongsongen_US
dc.date.accessioned2018-09-05T04:34:26Z-
dc.date.available2018-09-05T04:34:26Z-
dc.date.issued2018-07-01en_US
dc.identifier.issn16132254en_US
dc.identifier.issn13464523en_US
dc.identifier.other2-s2.0-85040224908en_US
dc.identifier.other10.1007/s10396-017-0856-8en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85040224908&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/58876-
dc.description.abstract© 2018, The Japan Society of Ultrasonics in Medicine. A 26-year-old pregnant woman was diagnosed with fetal bladder prolapse following rupture of a patent urachus/urachal cyst, based on the finding of cyst disappearance with replacement with an infra-umbilical, extra-abdominal solid soft-tissue mass, mimicking bladder exstrophy. The neonatal findings confirmed the prenatal diagnosis. The baby was healthy and had a successful surgical correction. This report provides clues to differentiating ruptured bladder prolapse from bladder exstrophy as follows: (1) well-documented urachal cyst with urine-filled mass in the early gestation, (2) development of solid soft-tissue mass shortly after disappearance of the urachal cyst, and (3) no other structural abnormalities (bladder exstrophy is usually associated with abnormal genitalia, epispadias, or pubic diastasis). This study underlines the differentiation between the two entities because of the vast difference in prognosis, management, and proper counseling.en_US
dc.subjectMedicineen_US
dc.titleProlapsed bladder following rupture of patent urachal cyst, mimicking bladder exstrophy: a case report and literature reviewen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Medical Ultrasonicsen_US
article.volume45en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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