A. Shamsuddin, P. Biswas, Muhammad Ishtiaque Sayeed Al Manzoo, M. Azad, Md Nurul Akhtar Hasan, Jasmin Hosain, Mohammad Sharifuzzaman Shamsuddin
{"title":"法洛四联症合并肺动脉瓣缺失综合征并左肺动脉缺失-一种罕见的表现","authors":"A. Shamsuddin, P. Biswas, Muhammad Ishtiaque Sayeed Al Manzoo, M. Azad, Md Nurul Akhtar Hasan, Jasmin Hosain, Mohammad Sharifuzzaman Shamsuddin","doi":"10.3329/bhj.v35i1.49148","DOIUrl":null,"url":null,"abstract":"Absent left pulmonary artery with Tetralogy of Fallot (TOF) with absent pulmonary valve syndrome (APVS), is a rare congenital cardiac anomaly. Here we present such a case of A 2 year 11 month old girl with cyanosis, exertional dyspnoea. Her diagnosis is confirmed by echocardiography and CT angiogram. There are very few cases have been reported till date with high postoperative mortality. Although per operative decision making was challenging regarding pulmonary valve and size of the RPA, we performed ICR with RPA reductionplasty and creation of monocuspid pulmonary valve with success. As it is a rare association and we have overcome the hindrance we came across per operatively, we are reporting this case. \nBangladesh Heart Journal 2020; 35(1) : 74-77","PeriodicalId":247590,"journal":{"name":"Bangladesh Heart Journal","volume":"8 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Tetralogy of Fallot with Absent Pulmonary Valve Syndrome with Absent Left Pulmonary Artery - A Rare Presentation\",\"authors\":\"A. Shamsuddin, P. Biswas, Muhammad Ishtiaque Sayeed Al Manzoo, M. Azad, Md Nurul Akhtar Hasan, Jasmin Hosain, Mohammad Sharifuzzaman Shamsuddin\",\"doi\":\"10.3329/bhj.v35i1.49148\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Absent left pulmonary artery with Tetralogy of Fallot (TOF) with absent pulmonary valve syndrome (APVS), is a rare congenital cardiac anomaly. Here we present such a case of A 2 year 11 month old girl with cyanosis, exertional dyspnoea. Her diagnosis is confirmed by echocardiography and CT angiogram. There are very few cases have been reported till date with high postoperative mortality. Although per operative decision making was challenging regarding pulmonary valve and size of the RPA, we performed ICR with RPA reductionplasty and creation of monocuspid pulmonary valve with success. As it is a rare association and we have overcome the hindrance we came across per operatively, we are reporting this case. \\nBangladesh Heart Journal 2020; 35(1) : 74-77\",\"PeriodicalId\":247590,\"journal\":{\"name\":\"Bangladesh Heart Journal\",\"volume\":\"8 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-09-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bangladesh Heart Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3329/bhj.v35i1.49148\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bangladesh Heart Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3329/bhj.v35i1.49148","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Tetralogy of Fallot with Absent Pulmonary Valve Syndrome with Absent Left Pulmonary Artery - A Rare Presentation
Absent left pulmonary artery with Tetralogy of Fallot (TOF) with absent pulmonary valve syndrome (APVS), is a rare congenital cardiac anomaly. Here we present such a case of A 2 year 11 month old girl with cyanosis, exertional dyspnoea. Her diagnosis is confirmed by echocardiography and CT angiogram. There are very few cases have been reported till date with high postoperative mortality. Although per operative decision making was challenging regarding pulmonary valve and size of the RPA, we performed ICR with RPA reductionplasty and creation of monocuspid pulmonary valve with success. As it is a rare association and we have overcome the hindrance we came across per operatively, we are reporting this case.
Bangladesh Heart Journal 2020; 35(1) : 74-77