https://scholars.lib.ntu.edu.tw/handle/123456789/538520
標題: | Left common carotid artery arising from the pulmonary artery in a patient with DiGeorge syndrome | 作者: | Huang S.-F. MEI-HWAN WU |
關鍵字: | aortic arch anomaly; congenital vascular anomaly; DiGeorge syndrome; tetralogy of Fallot | 公開日期: | 1996 | 出版社: | BMJ Publishing Group | 卷: | 76 | 期: | 1 | 起(迄)頁: | 82-83 | 來源出版物: | Heart | 摘要: | A female infant, born at 33 weeks' gestation with tetralogy of Fallot, died of severe perinatal asphyxia 6 hours after birth. Necropsy disclosed two associated vascular anomalies: a right aortic arch with a left common carotid artery arising from the pulmonary artery (isolated left common carotid artery) and an aberrant left subclavian artery arising from the descending aorta. Agenesis of the thymus and parathyroid gland was also found, suggesting that the child also had DiGeorge syndrome. Origin of the left common carotid artery from the pulmonary artery is exceedingly rare. When planning surgical treatment it is important to be aware of the possibility of this anomaly occurring in association with congenital heart disease, particularly in the presence of tetralogy of Fallot, right sided aortic arch, or DiGeorge syndrome. |
URI: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-0029837880&doi=10.1136%2fhrt.76.1.82&partnerID=40&md5=05faeaa0d45e193bb411e5f10df133b3 https://scholars.lib.ntu.edu.tw/handle/123456789/538520 |
ISSN: | 1355-6037 | DOI: | 10.1136/hrt.76.1.82 | SDG/關鍵字: | article; carotid artery anomaly; case report; DiGeorge syndrome; disease association; Fallot tetralogy; female; human; infant; left coronary artery; priority journal; pulmonary artery disease |
顯示於: | 醫學系 |
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