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Double aortic arch anomalies in Children: A Systematic 20-Year Single Center Study.
Kaldararova, M; Simkova, I; Varga, I; Tittel, P; Kardos, M; Ondriska, M; Vrsanska, V; Masura, J.
Afiliación
  • Kaldararova M; National Institute of Cardiovascular Diseases-Children's Cardiac Center, Limbova Street 1, Bratislava, 833 51, Slovakia.
  • Simkova I; Department of Cardiology and Angiology, Slovak Medical University and National Institute of Cardiovascular Diseases, Pod Krasnou horkou Street 1, Bratislava, 833 48, Slovakia.
  • Varga I; Institute of Histology and Embryology, Faculty of Medicine, Comenius University in Bratislava, Sasinkova Street 4, Bratislava, 811 08, Slovakia.
  • Tittel P; National Institute of Cardiovascular Diseases-Children's Cardiac Center, Limbova Street 1, Bratislava, 833 51, Slovakia.
  • Kardos M; National Institute of Cardiovascular Diseases-Children's Cardiac Center, Limbova Street 1, Bratislava, 833 51, Slovakia.
  • Ondriska M; Department of Radiology, Children's University Hospital, Limbova Street 1, Bratislava, 833 40, Slovakia.
  • Vrsanska V; National Institute of Cardiovascular Diseases-Children's Cardiac Center, Limbova Street 1, Bratislava, 833 51, Slovakia.
  • Masura J; National Institute of Cardiovascular Diseases-Children's Cardiac Center, Limbova Street 1, Bratislava, 833 51, Slovakia.
Clin Anat ; 30(7): 929-939, 2017 Oct.
Article en En | MEDLINE | ID: mdl-28726262
Aortic arch anomalies underlie numerous congenital disorders. Effectively diagnosing and treating them requires close understanding of cardiovascular embryology. As our Center serves the entire pediatric population of our country, we performed a comprehensive retrospective analysis of all aortic arch anomalies diagnosed at our Center over the past 20 years. We analyzed 40 children with aortic arch anomalies, distinguishing two defect types: Group 1 displayed ring-forming anomalies, and Group 2 other types of aortic arch anomalies that did not form a vascular ring. We performed detailed morphological analyses using echocardiography, angiography, computed tomography, or magnetic resonance imaging and generated a catalog of all aortic arch anomalies present. Group 1 was represented by 25 patients; 40% with persistent both aortic arches, and 60% with various forms of right aortic arch and an incomplete left aortic arch. Group 2 was represented by 15 patients with complex heart defects. On the basis of our dataset, the incidence of all aortic arch anomalies was 0.033%, and of ring-forming pathologies 0.021%. Although aortic arch anomalies are rare, it is important to diagnose them correctly. It is critical to distinguish ring-forming types. Although in complex defects the aortic arch anomaly represents only an additive diagnosis, its correct definition could be crucial for further management. Cumulatively, this unique, long-term study provides a systematic patient registry and offers critical epidemiological data to aid the study of rare congenital cardiovascular defects. Clin. Anat. 30:929-939, 2017. © 2017 Wiley Periodicals, Inc.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Aorta Torácica / Cardiopatías Congénitas Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Clin Anat Asunto de la revista: ANATOMIA Año: 2017 Tipo del documento: Article País de afiliación: Eslovaquia Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Aorta Torácica / Cardiopatías Congénitas Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Clin Anat Asunto de la revista: ANATOMIA Año: 2017 Tipo del documento: Article País de afiliación: Eslovaquia Pais de publicación: Estados Unidos