C. Riera-Kinkel, Sesbania Bocanegra-Flores, M. Rosas-Peralta, Gabriela B Sanchez, David Roldan-Morales, Jaime Salgado-Vázquez, A. Ramirez-Castañeda, Sebastián Izunza-Saldaña, D. López-Gallegos, H. Márquez-González, Moisés Jiménez-Santos, Lucelli Yañez-Gutierrez
{"title":"Scimitar Syndrome: Infra-Diaphragmatic Form a Novel Surgical Approach","authors":"C. Riera-Kinkel, Sesbania Bocanegra-Flores, M. Rosas-Peralta, Gabriela B Sanchez, David Roldan-Morales, Jaime Salgado-Vázquez, A. Ramirez-Castañeda, Sebastián Izunza-Saldaña, D. López-Gallegos, H. Márquez-González, Moisés Jiménez-Santos, Lucelli Yañez-Gutierrez","doi":"10.15226/2573-864x/4/2/00160","DOIUrl":null,"url":null,"abstract":"Scimitar syndrome is a complex malformation in which the main feature is a partial anomalous venous drainage of the right side toward the inferior vena cava or the portal system. There are anomalies associated in bronchopulmonary segmentation and vascular lung connections [1]. In 1836 in specimens of autopsy Cooper in London published the first description and later Chassinat in París [2, 3]. In 1949 Dotter et, al through angiocardiography shown the first clinical diagnosis where noted the particular appearance of the anomalous vein on x-ray of thorax [4]. Later Neill et, al in 1960 called the scimitar sign for describing this anomaly [5]. Drake and Lynch in 1950 performed the first surgical management of this disease [6]. Later the first physiological correction of anomalous venous drainage was published in 1956 by Kirklin et, al [7]. Finally Neill CA, et al. published the familial occurrence of Scimitar syndrome.","PeriodicalId":362247,"journal":{"name":"American Journal of Cardiovascular and Thoracic Surgery","volume":"19 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Cardiovascular and Thoracic Surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15226/2573-864x/4/2/00160","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Scimitar syndrome is a complex malformation in which the main feature is a partial anomalous venous drainage of the right side toward the inferior vena cava or the portal system. There are anomalies associated in bronchopulmonary segmentation and vascular lung connections [1]. In 1836 in specimens of autopsy Cooper in London published the first description and later Chassinat in París [2, 3]. In 1949 Dotter et, al through angiocardiography shown the first clinical diagnosis where noted the particular appearance of the anomalous vein on x-ray of thorax [4]. Later Neill et, al in 1960 called the scimitar sign for describing this anomaly [5]. Drake and Lynch in 1950 performed the first surgical management of this disease [6]. Later the first physiological correction of anomalous venous drainage was published in 1956 by Kirklin et, al [7]. Finally Neill CA, et al. published the familial occurrence of Scimitar syndrome.