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Images in paediatric cardiology最新文献

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Corience: A website dedicated to congenital heart defects. 一个专门研究先天性心脏缺陷的网站。
Images in paediatric cardiology Pub Date : 2010-10-01
K Specht
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引用次数: 0
The chest x-ray in congenital heart disease 3. 先天性心脏病的胸部x线检查
Images in paediatric cardiology Pub Date : 2010-10-01
J Somerville, V Grech
{"title":"The chest x-ray in congenital heart disease 3.","authors":"J Somerville, V Grech","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":89564,"journal":{"name":"Images in paediatric cardiology","volume":"12 4","pages":"3-7"},"PeriodicalIF":0.0,"publicationDate":"2010-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3228335/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30488954","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pneumopericardium due to long sheath during transcatheter closure of PFO. 经导管关闭PFO时由于长鞘引起的心包气肿。
Images in paediatric cardiology Pub Date : 2010-07-01
Fa Pac, E Kibar, Tb Polat, S Topaloglu
{"title":"Pneumopericardium due to long sheath during transcatheter closure of PFO.","authors":"Fa Pac, E Kibar, Tb Polat, S Topaloglu","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":89564,"journal":{"name":"Images in paediatric cardiology","volume":"12 3","pages":"1-2"},"PeriodicalIF":0.0,"publicationDate":"2010-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3228334/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30488951","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The caveats in the diagnosis of anomalous origin of left coronary artery from pulmonary artery (ALCAPA). 左冠状动脉起源于肺动脉异常(ALCAPA)诊断的注意事项。
Images in paediatric cardiology Pub Date : 2010-07-01
Mj Varghese, Ss Kothari
{"title":"The caveats in the diagnosis of anomalous origin of left coronary artery from pulmonary artery (ALCAPA).","authors":"Mj Varghese,&nbsp;Ss Kothari","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Anomalous origin of left coronary artery from pulmonary artery (ALCAPA) is an infrequent, well described, but important anomaly of the coronary origin. Early diagnosis and prompt surgical treatment of the disease can be life saving. However, there are several potential sources of error in the seemingly simple stereotype diagnostic pattern. We report a case of ALCAPA and allude to some of the caveats in the diagnosis of this entity.</p>","PeriodicalId":89564,"journal":{"name":"Images in paediatric cardiology","volume":"12 3","pages":"3-8"},"PeriodicalIF":0.0,"publicationDate":"2010-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3228333/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30488952","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
An unusual vascular ring: Origin of a ductus arteriosus from an aberrant right subclavian artery in a neonate with tetralogy of Fallot. 不寻常的血管环:法洛四联症新生儿右锁骨下动脉异常形成动脉导管。
Images in paediatric cardiology Pub Date : 2010-04-01
R Walsh, D Chowdhury, D Kholwadwala
{"title":"An unusual vascular ring: Origin of a ductus arteriosus from an aberrant right subclavian artery in a neonate with tetralogy of Fallot.","authors":"R Walsh,&nbsp;D Chowdhury,&nbsp;D Kholwadwala","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":89564,"journal":{"name":"Images in paediatric cardiology","volume":"12 2","pages":"1-4"},"PeriodicalIF":0.0,"publicationDate":"2010-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3228331/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30488949","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Diagnosis of aortic origin of a pulmonary artery by echocardiography. 超声心动图对肺动脉主动脉起源的诊断。
Images in paediatric cardiology Pub Date : 2010-04-01
A Taksande, E Thomas, V Gautami, Ks Murthy
{"title":"Diagnosis of aortic origin of a pulmonary artery by echocardiography.","authors":"A Taksande,&nbsp;E Thomas,&nbsp;V Gautami,&nbsp;Ks Murthy","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The aortic origin of right or left branch pulmonary artery is a rare cardiac anomaly in which the right pulmonary artery usually arises from the ascending aorta just above the aortic sinuses, whereas the main pulmonary artery and the other pulmonary branch arise in their normal position. We report a rare case of isolated origin of right pulmonary artery from the ascending aorta.</p>","PeriodicalId":89564,"journal":{"name":"Images in paediatric cardiology","volume":"12 2","pages":"5-9"},"PeriodicalIF":0.0,"publicationDate":"2010-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3228332/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30488950","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The chest x-ray in congenital heart disease 2. 先天性心脏病的胸部x线检查
Images in paediatric cardiology Pub Date : 2010-01-01
J Somerville, V Grech
{"title":"The chest x-ray in congenital heart disease 2.","authors":"J Somerville,&nbsp;V Grech","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":89564,"journal":{"name":"Images in paediatric cardiology","volume":"12 1","pages":"1-8"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3228330/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30488947","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Symptomatic giant left atrial aneurysm in a child: a rare entity. 儿童有症状的巨大左心房动脉瘤:罕见病例。
Images in paediatric cardiology Pub Date : 2010-01-01
N Awasthy, M Tomar, S Radhakrishnan, S Shrivastava, Ks Iyer
{"title":"Symptomatic giant left atrial aneurysm in a child: a rare entity.","authors":"N Awasthy,&nbsp;M Tomar,&nbsp;S Radhakrishnan,&nbsp;S Shrivastava,&nbsp;Ks Iyer","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Isolated left atrial aneurysms are rare entities in clinical practice. Usually the condition is diagnosed in the second to fourth decades of life. The presence of such lesions in the pediatric age group is scantily described. We present a 2 year boy who presented with complaints of excessive irritability, respiratory distress and swelling of the feet. On examination, child was tachypnoeic with irregularly irregular rhythm. Echo showed a huge aneurysmal LA appendage with severe left ventricle dysfunction. The child underwent surgical resection for same. Findings were confirmed intraoperatively but he continued to have low cardiac output state after the surgery, with frequent arrhythmias and expired on day 7 of surgery. The case is reviewed and compared with the available English literature.</p>","PeriodicalId":89564,"journal":{"name":"Images in paediatric cardiology","volume":"12 1","pages":"9-13"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3228329/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30488948","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Fungal endocarditis in a premature infant complicated by a right atrial mycetoma and inferior vena cava thrombosis. 真菌性心内膜炎并发右心房足菌肿及下腔静脉血栓1例。
Images in paediatric cardiology Pub Date : 2009-10-01
J Sharma, A Nagraj, D Allapathi, B Rajegowda, R Leggiadro
{"title":"Fungal endocarditis in a premature infant complicated by a right atrial mycetoma and inferior vena cava thrombosis.","authors":"J Sharma,&nbsp;A Nagraj,&nbsp;D Allapathi,&nbsp;B Rajegowda,&nbsp;R Leggiadro","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The incidence of fungal endocarditis in premature infants is on the rise, reported in the last decade secondary to use of central venous lines, the frequent use of broad spectrum antibiotics and neonatal surgical interventions. Central line related thrombosis is a significant risk factor for persistent fungemia and end organ complications including endocarditis. We present a fatal case of progressive thrombosis of the inferior vena cava and right atrial mycetoma in a premature infant with candidemia who underwent ileostomy for bowel perforation. Renal failure occurred secondary to inferior vena cava thrombosis and right atrial mycetoma, both of which had a potential for hemodynamic compromise and embolism.</p>","PeriodicalId":89564,"journal":{"name":"Images in paediatric cardiology","volume":"11 4","pages":"6-11"},"PeriodicalIF":0.0,"publicationDate":"2009-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3228327/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30488946","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Biventricular noncompaction: A rare cause of fetal distress and tricuspid regurgitation. 双心室不压实:一个罕见的原因胎儿窘迫和三尖瓣反流。
Images in paediatric cardiology Pub Date : 2009-10-01
M Tomar, S Radhakrishnan
{"title":"Biventricular noncompaction: A rare cause of fetal distress and tricuspid regurgitation.","authors":"M Tomar,&nbsp;S Radhakrishnan","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Isolated noncompaction of the ventricular myocardium involving both ventricles is a rare entity. Here we report a rare case of biventricular noncompaction presenting with features of fetal distress and moderate tricuspid regurgitation. Noncompaction of both ventricles was diagnosed at birth.</p>","PeriodicalId":89564,"journal":{"name":"Images in paediatric cardiology","volume":"11 4","pages":"1-5"},"PeriodicalIF":0.0,"publicationDate":"2009-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3228328/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30488945","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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