Fetal aortopulmonary window: case series and review of the literature
ABSTRACT Aortopulmonary window is a rare congenital cardiac anomaly characterized by communication between the aorta and the pulmonary artery above the semilunar valves. Prenatal diagnosis is rare. We report four fetuses with aortopulmonary window and review the relevant literature. Approximately ha...
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| Veröffentlicht in: | Ultrasound in obstetrics & gynecology 2017-04, Vol.49 (4), p.533-539 |
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| container_title | Ultrasound in obstetrics & gynecology |
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| creator | Fotaki, A. Novaes, J. Jicinska, H. Carvalho, J. S. |
| description | ABSTRACT
Aortopulmonary window is a rare congenital cardiac anomaly characterized by communication between the aorta and the pulmonary artery above the semilunar valves. Prenatal diagnosis is rare. We report four fetuses with aortopulmonary window and review the relevant literature. Approximately half of the reported cases had additional cardiac defects. None had chromosomal abnormalities. In cases with normal cardiac connections, the diagnosis can be made prenatally on the standard three‐vessel view, as seen in two of our cases. In one fetus with complete transposition of the great arteries, the diagnosis was made retrospectively on sagittal views. In the remaining case, the window was seen postnatally but could not be identified retrospectively due to the abnormal superoinferior relationship of the ventricles and vessels. Copyright © 2016 ISUOG. Published by John Wiley & Sons Ltd. |
| doi_str_mv | 10.1002/uog.15936 |
| format | Article |
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Aortopulmonary window is a rare congenital cardiac anomaly characterized by communication between the aorta and the pulmonary artery above the semilunar valves. Prenatal diagnosis is rare. We report four fetuses with aortopulmonary window and review the relevant literature. Approximately half of the reported cases had additional cardiac defects. None had chromosomal abnormalities. In cases with normal cardiac connections, the diagnosis can be made prenatally on the standard three‐vessel view, as seen in two of our cases. In one fetus with complete transposition of the great arteries, the diagnosis was made retrospectively on sagittal views. In the remaining case, the window was seen postnatally but could not be identified retrospectively due to the abnormal superoinferior relationship of the ventricles and vessels. Copyright © 2016 ISUOG. Published by John Wiley & Sons Ltd.</description><identifier>ISSN: 0960-7692</identifier><identifier>EISSN: 1469-0705</identifier><identifier>DOI: 10.1002/uog.15936</identifier><identifier>PMID: 27063344</identifier><identifier>CODEN: UOGYFJ</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Abnormalities ; Adult ; Aorta ; Aorta, Thoracic - abnormalities ; Aorta, Thoracic - diagnostic imaging ; Aorta, Thoracic - embryology ; aortopulmonary window ; Chromosome aberrations ; congenital heart defects ; Diagnosis ; Early Diagnosis ; echocardiography ; Echocardiography - methods ; Female ; fetus ; Fetuses ; Heart ; Heart Defects, Congenital - diagnostic imaging ; Humans ; Literature reviews ; Medical diagnosis ; Prenatal diagnosis ; Prenatal Diagnosis - methods ; Prospective Studies ; Pulmonary artery ; Pulmonary Artery - abnormalities ; Pulmonary Artery - diagnostic imaging ; Pulmonary Artery - embryology ; Sensitivity and Specificity ; Transposition ; Ultrasonic imaging</subject><ispartof>Ultrasound in obstetrics & gynecology, 2017-04, Vol.49 (4), p.533-539</ispartof><rights>Copyright © 2016 ISUOG. Published by John Wiley & Sons Ltd.</rights><rights>Copyright © 2017 ISUOG. Published by John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4156-badc7624220de312c4060502bf27fb525cb08699fecaf0d967b5558ca56617cc3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fuog.15936$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fuog.15936$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,1434,27926,27927,45576,45577,46411,46835</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27063344$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fotaki, A.</creatorcontrib><creatorcontrib>Novaes, J.</creatorcontrib><creatorcontrib>Jicinska, H.</creatorcontrib><creatorcontrib>Carvalho, J. S.</creatorcontrib><title>Fetal aortopulmonary window: case series and review of the literature</title><title>Ultrasound in obstetrics & gynecology</title><addtitle>Ultrasound Obstet Gynecol</addtitle><description>ABSTRACT
Aortopulmonary window is a rare congenital cardiac anomaly characterized by communication between the aorta and the pulmonary artery above the semilunar valves. Prenatal diagnosis is rare. We report four fetuses with aortopulmonary window and review the relevant literature. Approximately half of the reported cases had additional cardiac defects. None had chromosomal abnormalities. In cases with normal cardiac connections, the diagnosis can be made prenatally on the standard three‐vessel view, as seen in two of our cases. In one fetus with complete transposition of the great arteries, the diagnosis was made retrospectively on sagittal views. In the remaining case, the window was seen postnatally but could not be identified retrospectively due to the abnormal superoinferior relationship of the ventricles and vessels. Copyright © 2016 ISUOG. Published by John Wiley & Sons Ltd.</description><subject>Abnormalities</subject><subject>Adult</subject><subject>Aorta</subject><subject>Aorta, Thoracic - abnormalities</subject><subject>Aorta, Thoracic - diagnostic imaging</subject><subject>Aorta, Thoracic - embryology</subject><subject>aortopulmonary window</subject><subject>Chromosome aberrations</subject><subject>congenital heart defects</subject><subject>Diagnosis</subject><subject>Early Diagnosis</subject><subject>echocardiography</subject><subject>Echocardiography - methods</subject><subject>Female</subject><subject>fetus</subject><subject>Fetuses</subject><subject>Heart</subject><subject>Heart Defects, Congenital - diagnostic imaging</subject><subject>Humans</subject><subject>Literature reviews</subject><subject>Medical diagnosis</subject><subject>Prenatal diagnosis</subject><subject>Prenatal Diagnosis - methods</subject><subject>Prospective Studies</subject><subject>Pulmonary artery</subject><subject>Pulmonary Artery - abnormalities</subject><subject>Pulmonary Artery - diagnostic imaging</subject><subject>Pulmonary Artery - embryology</subject><subject>Sensitivity and Specificity</subject><subject>Transposition</subject><subject>Ultrasonic imaging</subject><issn>0960-7692</issn><issn>1469-0705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqN0U1r3DAQBmARWrqbtIf-gSLoJRcnI8kaWb2FJV8QyKU5C1kep1681lays-y_j7NJe-gh9KQBPQwz8zL2VcCZAJDnU3w8E9oqPGJLUaItwID-wJZgEQqDVi7Ycc5rAMBS4Se2kAZQqbJcsssrGn3PfUxj3E79Jg4-7fmuG5q4-8GDz8QzpY4y90PDEz11tOOx5eMv4n03UvLjlOgz-9j6PtOXt_eEPVxd_lzdFHf317eri7silEJjUfsmGJSllNCQEjKUgKBB1q00ba2lDjVUaG1LwbfQWDS11roKXiMKE4I6Yaevfbcp_p4oj27T5UB97weKU3aisqIyRlb6P6hERFWhmen3f-g6TmmYF3EKECVIFPY9JapKKZzHlbP69qamekON26ZuM1_U_bn4DM5fwa7raf_3X4B7idLNUbpDlO7h_vpQqGdMA425</recordid><startdate>201704</startdate><enddate>201704</enddate><creator>Fotaki, A.</creator><creator>Novaes, J.</creator><creator>Jicinska, H.</creator><creator>Carvalho, J. 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Aortopulmonary window is a rare congenital cardiac anomaly characterized by communication between the aorta and the pulmonary artery above the semilunar valves. Prenatal diagnosis is rare. We report four fetuses with aortopulmonary window and review the relevant literature. Approximately half of the reported cases had additional cardiac defects. None had chromosomal abnormalities. In cases with normal cardiac connections, the diagnosis can be made prenatally on the standard three‐vessel view, as seen in two of our cases. In one fetus with complete transposition of the great arteries, the diagnosis was made retrospectively on sagittal views. In the remaining case, the window was seen postnatally but could not be identified retrospectively due to the abnormal superoinferior relationship of the ventricles and vessels. Copyright © 2016 ISUOG. Published by John Wiley & Sons Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>27063344</pmid><doi>10.1002/uog.15936</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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| subjects | Abnormalities Adult Aorta Aorta, Thoracic - abnormalities Aorta, Thoracic - diagnostic imaging Aorta, Thoracic - embryology aortopulmonary window Chromosome aberrations congenital heart defects Diagnosis Early Diagnosis echocardiography Echocardiography - methods Female fetus Fetuses Heart Heart Defects, Congenital - diagnostic imaging Humans Literature reviews Medical diagnosis Prenatal diagnosis Prenatal Diagnosis - methods Prospective Studies Pulmonary artery Pulmonary Artery - abnormalities Pulmonary Artery - diagnostic imaging Pulmonary Artery - embryology Sensitivity and Specificity Transposition Ultrasonic imaging |
| title | Fetal aortopulmonary window: case series and review of the literature |
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