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dc.contributor.authorKasemsri Srisupunditen_US
dc.contributor.authorKornkanok Sukpanen_US
dc.contributor.authorTheera Tongsongen_US
dc.contributor.authorKuntharee Traisrisilpen_US
dc.date.accessioned2020-10-14T08:41:04Z-
dc.date.available2020-10-14T08:41:04Z-
dc.date.issued2020-09-01en_US
dc.identifier.issn10970096en_US
dc.identifier.issn00912751en_US
dc.identifier.other2-s2.0-85085966159en_US
dc.identifier.other10.1002/jcu.22876en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85085966159&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/70772-
dc.description.abstract© 2020 Wiley Periodicals, Inc. Mediastinal teratoma can cause severe hydrops fetalis, which worsens the effects of the mass compression on the vital mediastinal organs. A careful sonographic examination is mandatory to demonstrate the characteristic features suggestive of this congenital tumor. We describe these features at 20 weeks gestation. The most prominent finding was the heterogeneous echogenicity of a large cystic-solid mass with hyperechoic dots, seen as a part of the anterior mediastinum immediately posterior to the sternum. Additional diagnostic features included posterior displacement of the heart, low cardiac output, and hypoplasia of the normally structured heart and lungs due to the direct mass compression. These sonographic findings were confirmed at autopsy which confirmed a nonmetastatic immature teratoma. Sonography may enable accurate diagnosis of mediastinal teratoma considering the anterior location and heterogeneous appearance of the mass, posterior displacement of the heart, normal lung morphology, and compression effects on these organs.en_US
dc.subjectMedicineen_US
dc.titlePrenatal sonographic features of fetal mediastinal teratomaen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Clinical Ultrasounden_US
article.volume48en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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