Association Between Tetralogy of Fallot and Tracheobronchial Branching Abnormalities: A New Clue for Pathogenesis?

机译：法洛四联症与气管支气管分支异常之间的关联：发病机制的新线索吗？

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BackgroundIn our practice, we noticed an increased frequency of tracheobronchial branching abnormalities (TBAs) in patients with tetralogy of Fallot (ToF). This study aimed to determine whether an association exists between congenital TBAs and ToF with or without pulmonary atresia.

机译：背景在我们的实践中，我们发现患有法洛四联症（ToF）的患者气管支气管分支异常（TBA）的频率增加。这项研究旨在确定先天性TBA与ToF伴或不伴肺动脉闭锁之间是否存在关联。

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期刊名称 Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
作者
Guillaume Chassagnon; Bruno Lefort; Mathilde Meot; Elodie Carpentier; Dominique Sirinelli; Alain Chantepie; Baptiste Morel;
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作者单位

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年(卷),期 2018(7),1
年度 2018
页码 e006921
总页数 7
原文格式 PDF
正文语种
中图分类心血管疾病;
关键词
computed tomography congenital heart disease pulmonary atresia tetralogy of Fallot tracheobronchial branching abnormalities;

机译：计算机体层摄影术;先天性心脏病;肺动脉闭锁;法洛四联症;气管支气管分支异常;
入库时间 2022-08-21 11:02:03

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1. Adult Nigerian With Untreated Tetralogy Of Fallot- A Case Report Background: Tetralogy of Fallot (TOF) is the most common form of cyanotic congenital heart .. Unlike in the western world where adult TOF is a rarity, in the developing countries without cardiac surgical centers and inadequate medical treatment, patients die early so adult untreated TOF is worth reporting. A 23 year old man presented with chest pains of 18 months, exertional dyspnea, palpitations and a history of squatting since childhood. Examination revealed central cyanosis, grade 4 digital clubbing, with pansystolic and ejection systolic murmurs over tricuspid and pulmonary areas.RESULTS : Chest radiograph, Electrocardiogram (ECG ) and Echocardiograms confirmed Tetralogy of Fallot [J] . Uchenna D.I., Jesuorobo D. E. The Internet Journal of Cardiology . 2012,第2期

机译：成年尼日利亚人患有未经治疗的法洛四联症-病例报告背景：法洛四联症（TOF）是发性先天性心脏病的最常见形式..与西方世界不同，成年TOF很少见，在没有心脏外科手术中心的发展中国家而且医疗不充分，患者会早逝，因此成人未经治疗的TOF值得报告。一名23岁的男子自18岁起出现18个月的胸痛，劳累性呼吸困难，心和蹲下史。检查发现中央紫cyan，四级数字俱乐部，在三尖瓣和肺部区域出现全收缩期和射血期收缩期杂音。
2. Silencing mutations in JAG1 gene may play crucial roles in the pathogenesis of Tetralogy of Fallot [J] . Safari-Arababadi Amin, Behjati-Ardakani Mostafa, Kalantar Seyed Mehdi, Cellular and molecular biology . 2018,第4期

机译：JAG1基因中的沉默突变可能在椎间盘四十型发病机制中起重要作用
3. Effect of Losartan on Right Ventricular Dysfunction Results From the Double-Blind, Randomized REDEFINE Trial (Right Ventricular Dysfunction in Tetralogy of Fallot: Inhibition of the Renin-Angiotensin-Aldosterone System) in Adults With Repaired Tetralogy of Fallot [J] . Bokma Jouke P., Winter Michiel M., van Dijk Arie P., Circulation: An Official Journal of the American Heart Association . 2018,第14期

机译：氯沙坦对右心室功能障碍的影响来自双盲，随机重新定义（Tetralogy的右心室功能障碍：抑制Renin-ungiotensin-aldosterone系统）在成人中进行修复的Tetralogy
4. Can Laplacian Eigenmaps Be Used for Differentiation Between Healthy Subjects and Patients With Corrected Tetralogy of Fallot? [C] . Ben Jacobs, Amalia Villa, Jonathan Moeyersons, Computing in Cardiology . 2020

机译：Laplacian eIgenmaps可以用于健康受试者和患者矫正Tetralogy的椎间盘突出之间的差异吗？
5. Prognostic Implications of Inferior Vena Cava Hemodynamics in Ambulatory Patients with Tetralogy of Fallot [D] . Egbe, Alexander C. 2020

机译：下腔静脉血流动力学在椎间盘突出的动态患者中的预后意义
6. Right bundle branch block pattern after uncomplicated right ventricular outflow tract pacing in a patient with a left sided superior vena cava and corrected tetralogy of Fallot [O] . Anunay Gupta, Neeraj Parakh, Rajnish Juneja 2018

机译：左侧上腔静脉并校正了法洛四联症患者的无并发症右心室流出道起搏后的右束支传导阻滞模式
7. Association Between Tetralogy of Fallot and Tracheobronchial Branching Abnormalities: A New Clue for Pathogenesis? [O] . Guillaume Chassagnon, Bruno Lefort, Mathilde Meot, 2018

机译：Tetralogy之间的结合和气管支气管分支异常：发病机制的新线索？

Association Between Tetralogy of Fallot and Tracheobronchial Branching Abnormalities: A New Clue for Pathogenesis?

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