1,010 results match your criteria Cor Triatriatum


Endoscopic Repair of Obstructive Cor Triatriatum.

CASE (Phila) 2020 Apr 6;4(2):82-85. Epub 2019 Dec 6.

Division of Cardiac Surgery, Western University, London, Ontario, Canada.

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http://dx.doi.org/10.1016/j.case.2019.11.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175808PMC

Anesthetic experience during a laparoscopic appendectomy in a pregnant patient with isolated cor triatriatum sinister.

Saudi J Anaesth 2020 Apr-Jun;14(2):257-260. Epub 2020 Mar 5.

Department of Anesthesiology and Pain Medicine, Ilsan Paik Hospital, Inje University School of Medicine, Ilsan, Korea.

A 39-year-old pregnant patient with acute appendicitis was planned for emergency laparoscopic appendectomy in the second trimester of pregnancy. Preoperative two-dimensional transthoracic echocardiography revealed asymptomatic cor triatriatum sinisiter (CTS), dividing left atrium into two chambers. There was no associated cardiac anomaly, wall motion abnormality, or pulmonary hypertension. Read More

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http://dx.doi.org/10.4103/sja.SJA_816_19DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164453PMC

Atrial fibrillation cryoablation in cor triatriatum dexter.

Europace 2020 Apr 15. Epub 2020 Apr 15.

Department of Cardiology, Mitera General Hospital, Hygeia Group, 6, Erithrou Stavrou, Maroussi, Athens 15123, Greece.

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http://dx.doi.org/10.1093/europace/euaa061DOI Listing

Cor Triatriatum Sinister (Divided Left Atrium): Histopathologic Features and Clinical Management.

Ann Thorac Surg 2020 Feb 28. Epub 2020 Feb 28.

Aswan Heart Center, Aswan Governate, Egypt; Department of Cardiac Surgery, Royal Brompton and Harefield National Health Service Trust, London, United Kingdom. Electronic address:

Background: Cor triatriatum sinister (CTS), or divided left atrium, is a rare congenital cardiac disease in which the left atrium is divided into 2 chambers by a fibromuscular diaphragm that will cause blood flow obstruction to the left ventricle. Recent animal studies suggested the role of hyaluronidase-2 (HYAL-2) deficiency as a risk factor for developing CTS. The histopathologic features of this diaphragm and our surgical experience with the management of this disease are reviewed. Read More

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http://dx.doi.org/10.1016/j.athoracsur.2020.01.025DOI Listing
February 2020

Cor triatriatum sinister mimicking mitral stenosis.

Turk Gogus Kalp Damar Cerrahisi Derg 2019 Apr 24;27(2):261-262. Epub 2019 Apr 24.

Department of Pediatric Cardiology, Tepecik Training and Research Hospital, İzmir, Turkey.

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http://dx.doi.org/10.5606/tgkdc.dergisi.2019.16350DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7021386PMC

Multimodality imaging of an asymptomatic giant right atrial appendage aneurysm.

Echocardiography 2020 Feb 22;37(2):347-350. Epub 2020 Jan 22.

Department of Cardiology, Mehmet Akif Ersoy Thoracic and Cardiovascular Surgery Training and Research Hospital, Istanbul, Turkey.

Right atrial appendage (RAA) aneurysm is a rare congenital cardiac abnormality thought to be caused by dysplasia of the muscular wall of the RA and RAA. Structural, contractile, or electrical atrial changes are associated with the onset and progression of atrial fibrillation. The RAA aneurysm can have various symptoms, such as thromboembolic complications. Read More

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http://dx.doi.org/10.1111/echo.14595DOI Listing
February 2020

A Systematic Review of a Long-forgotten Cause of Atrial Fibrillation and Stroke: Cor Triatriatum.

Cureus 2019 Dec 13;11(12):e6371. Epub 2019 Dec 13.

Internal Medicine, Services Institute of Medical Sciences, Lahore, PAK.

Cor triatriatum is a rare congenital cardiac condition characterized by the division of one atrium into two chambers by a fibromuscular membrane, resulting in three atrial chambers. The goal of this study was to determine the associations of cor triatriatum with cyanosis, atrial fibrillation (AF), and stroke. MEDLINE (PubMed, Ovid), Embase, and Cochrane databases were searched on April 25, 2019, for relevant articles on cor triatriatum. Read More

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http://dx.doi.org/10.7759/cureus.6371DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6957057PMC
December 2019

Case report - azygos vein drainage into the left atrium in a dog with cor triatriatum dexter and a patent foramen ovale.

J Vet Cardiol 2019 Dec 10;26:1-9. Epub 2019 Oct 10.

Division of Cardiology, From the Vetsuisse Faculty University of Zurich, Winterthurerstrasse 260, 8057, Zurich, Switzerland.

A 2-year-old Airedale terrier was presented with exercise intolerance since birth and newly developed chylous pleural effusion. Imaging procedures including echocardiography, cardiac magnetic resonance imaging, computed tomography, and selective angiography revealed an aberrant connection of the azygos vein and the left atrium, a membrane in the right atrium consistent with cor triatriatum dexter, and a patent foramen ovale with right-to-left shunt. Balloon dilation of the membrane in the right atrium seemed to result in transient improvement of exercise tolerance compared with the previous 2 years. Read More

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http://dx.doi.org/10.1016/j.jvc.2019.09.002DOI Listing
December 2019

Cor Triatriatum Dexter as an Incidental Finding: Role of Two-Dimensional Transthoracic Echocardiography.

Cureus 2019 Sep 17;11(9):e5683. Epub 2019 Sep 17.

Cardiology, Mount Sinai Hospital, New-York City, USA.

Cor triatriatum dexter (CTD) is a rare congenital cardiac anomaly in which a membranous structure divides the right atrium (RA) into two chambers. Persistence of the right valve of the sinus venosus, which usually regresses as a part of normal embryological development, is responsible for membranous partition. There is a high incidence of right-sided congenital abnormalities of the heart associated with this condition. Read More

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http://dx.doi.org/10.7759/cureus.5683DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6823002PMC
September 2019

'Cor triatriatum', or divided left atrium.

Heart 2020 Feb 9;106(3):242. Epub 2019 Oct 9.

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http://dx.doi.org/10.1136/heartjnl-2019-315812DOI Listing
February 2020
1 Read

The strange case of congenital mitral stenosis in an adult man with cor triatriatum.

Echocardiography 2019 11 1;36(11):2122-2125. Epub 2019 Oct 1.

Department of Internal Medicine, Fondazione Policlinico Universitario A.Gemelli IRCCS, Catholic University of the Sacred Heart School of Medicine, Rome, Italy.

We report the case of a 74-year-old male, with a medical history of cor triatriatum, admitted with a 10-day history of intermittent fever. Three sets of blood cultures were positive for Providencia rettgeri. Transthoracic and transesophageal echocardiogram excluded infective endocarditis, but revealed a congenital accessory tissue adhering to the mitral valve, causing supravalvular mitral stenosis. Read More

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http://dx.doi.org/10.1111/echo.14497DOI Listing
November 2019
2 Reads

Hybrid balloon dilation treatment for cor triatriatum dexter in a small breed puppy.

J Vet Sci 2019 Sep;20(5):e49

Department of Veterinary Surgery, Faculty of Veterinary Medicine, Tokyo University of Agriculture and Technology, Tokyo 183-8509, Japan.

The authors encountered a 4-month-old, female Shiba dog weighing 4.0 kg, who had been exhibiting abdominal distension and increasing ascites for 2 months. She was brought for further examination and treatment with the chief complaints of ascites and dyspnoea during sleep. Read More

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http://dx.doi.org/10.4142/jvs.2019.20.e49DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6769332PMC
September 2019
2 Reads

Cor triatriatum dexter associated with atrial septal defect and mitral valve regurgitation.

J Echocardiogr 2019 Sep 23. Epub 2019 Sep 23.

Division of Cardiology, Shimane University Faculty of Medicine, Izumo, 693-8501, Japan.

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http://dx.doi.org/10.1007/s12574-019-00444-xDOI Listing
September 2019
2 Reads

Successful balloon valvuloplasty of a subpulmonic membrane associated with cor triatriatum dexter: a case report.

J Med Case Rep 2019 Sep 15;13(1):291. Epub 2019 Sep 15.

Cardiology Department, Hospital University Ibn Rochd, Casablanca, Morocco.

Background: Subpulmonic membrane as a cause of right ventricular outflow tract obstruction in patients with concordant ventriculoarterial connection and intact ventricular septum is considered to be rare. Association with cor triatriatum dexter and success of subpulmonic balloon valvuloplasty have never been reported, at least to the best of our knowledge.

Case Presentation: A 3-year-old Moroccan boy was referred to our tertiary care hospital with complaints of dyspnea on moderate exertion. Read More

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https://jmedicalcasereports.biomedcentral.com/articles/10.11
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http://dx.doi.org/10.1186/s13256-019-2218-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745068PMC
September 2019
6 Reads

A Rare Case of Cardiogenic Shock: Cor Triatriatum With Anomalous Pulmonary Venous Return.

World J Pediatr Congenit Heart Surg 2019 09;10(5):651-653

Department of Pediatric Cardiovascular Surgery, Hospital Sant Joan de Dèu, University of Barcelona, Barcelona, Spain.

Obstructive total anomalous pulmonary venous return (TAPVR) is a potentially life-threatening clinical condition and a surgical emergency. Left-sided partial anomalous pulmonary venous return (PAPVR) in association with a subdivided left atrium, also known as cor triatriatum sinister (CTS), is a very rare malformation that can mimic obstructive TAPVR. We present a case of a newborn with clinical manifestation of cardiogenic shock caused by CTS and PAPVR. Read More

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http://dx.doi.org/10.1177/2150135119867592DOI Listing
September 2019
3 Reads

Surgical experience with cor triatriatum repair beyond infancy.

J Card Surg 2019 Dec 3;34(12):1445-1451. Epub 2019 Sep 3.

Department of Cardiothoracic and Vascular Surgery, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Background: Cor triatriatum is an exceedingly rare congenital heart defect which can present at any age depending upon the presence of associated cardiac anomalies and the size of communication between the common chamber and the left atrium. Our aim is to present 10 years surgical outcome of cor triatriatum repair in patients who present beyond infancy.

Methods: On going through our institute's surgical database from January 2009 to June 2019 for cor triatriatum, 14 patients were found to have undergone the surgical correction. Read More

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http://dx.doi.org/10.1111/jocs.14237DOI Listing
December 2019
4 Reads

Cor triatriatum sinister in a dog.

J Vet Cardiol 2019 Oct 25;25:25-31. Epub 2019 Jul 25.

Department of Veterinary Medical Sciences, Alma Mater Studiorum - University of Bologna, Italy. Electronic address:

This report describes the transthoracic and transesophageal echocardiographic features of cor triatriatum sinister in an asymptomatic 6-year-old male French bulldog. Although cor triatriatum sinister represents a well-known and widely described cardiac malformation in humans, its description in the canine population is rare. In this clinical case, non-invasive echocardiographic techniques were helpful in visualizing and characterizing the lesion, allowing a valuable assessment of the malformation, and its hemodynamic consequences. Read More

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http://dx.doi.org/10.1016/j.jvc.2019.07.003DOI Listing
October 2019
4 Reads

Combined interventional procedure and cardiopulmonary bypass surgery in a dog with cor triatriatum dexter, patent foramen ovale, and pulmonary stenosis.

J Vet Intern Med 2019 Sep 5;33(5):2227-2234. Epub 2019 Aug 5.

Istituto Veterinario di Novara, Novara, Italy.

A 2-year-old American Pit Bull dog was presented for surgical evaluation of imperforate cor triatriatum dexter (CTD) and patent foramen ovale (PFO). Echocardiography identified an imperforate CTD associated with a right-to-left shunting PFO and valvular pulmonary stenosis. A 2-step interventional and surgical approach was used. Read More

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http://dx.doi.org/10.1111/jvim.15580DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6766562PMC
September 2019
4 Reads

Cor triatriatum with extremely severe right ventricular pressure in an infant.

J Card Surg 2019 10 2;34(10):1092-1093. Epub 2019 Aug 2.

Department of Cardiovascular Surgery, West China Hospital, Sichuan University, Chengdu, P.R. China.

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http://dx.doi.org/10.1111/jocs.14165DOI Listing
October 2019
2 Reads

Bands in the Heart: Multimodality Imaging Review.

Radiographics 2019 Sep-Oct;39(5):1238-1263. Epub 2019 Aug 2.

From the Cardiothoracic Imaging Division, Department of Radiology (P.R., H.G.), Cardiology Division, Department of Internal Medicine, (J.M.), UT Southwestern Medical Center, 5323 Harry Hines Blvd, E6.122G, Mail Code 9316, Dallas, TX 75390-8896; Department of Radiology, University of Rochester Medical Center, Rochester, NY (A.C.); Department of Pediatric Cardiology, Stead Family Children's Hospital, Iowa City, Iowa (R.A.); Department of Radiology, Summa Akron City Hospital, Akron, Ohio (N.L.F.); Department of Radiology, Mexican Institute of Social Security Western National Medical Center, IMSS, Guadalajara, Mexico (H.G.); and Department of Radiology, Imaging and Diagnostic Center, Guadalajara, Mexico (H.G.).

Multiple bands and bandlike structures can be found within the cardiac chambers, which can be evaluated with various imaging modalities including echocardiography, CT, MRI, and invasive angiography. These bands can be classified as normal structures or normal variants, aberrant structures, or pathologic entities. Normal structures include the crista terminalis, taenia sagittalis, Chiari network, coumadin ridge, moderator band, papillary muscles, and chordae tendineae. Read More

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http://dx.doi.org/10.1148/rg.2019180176DOI Listing
May 2020
5 Reads
2.602 Impact Factor

Acute Pulmonary Hypertension During Pregnancy Caused by Isolated Cor Triatriatum Sinus With Left Atrial Thrombus.

Circ Cardiovasc Imaging 2019 08 29;12(8):e009331. Epub 2019 Jul 29.

Department of Ultrasound, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China (L.J., W.W., Z.S., B.W., Q.L., Y.L., L.Z., M.X.).

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http://dx.doi.org/10.1161/CIRCIMAGING.119.009331DOI Listing
August 2019
2 Reads

A rare case of an isolated aneurysmal supravalvar mitral ring in a young Nigerian adult: a cor-triatriatum mimic.

Oxf Med Case Reports 2019 Jun 24;2019(6):omz050. Epub 2019 Jun 24.

Department of Paediatrics, Lagos University Teaching Hospital, PMB, Lagos, Nigeria.

Supravalvar mitral ring is a rare congenital abnormality characterized by a ridge of connective tissue located above the mitral valve. It is a cause of congenital mitral stenosis typically presenting in childhood and usually associated with other cardiac abnormalities. We report the rare case of a 24-year-old male presenting with an isolated aneurysmal supravalvar mitral ring. Read More

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http://dx.doi.org/10.1093/omcr/omz050DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6600123PMC
June 2019
2 Reads

[Adult Cor Triatriatum Found by Chance at the Onset of Myocardial Infarction].

Kyobu Geka 2019 Jun;72(6):414-417

Department of Cardiovascular Surgery, Toyohashi Municipal Hospital, Toyohashi, Japan.

Cor triatriatum sinister is a rare congenital heart disease in which the left atrium is divided into 2 chambers by a membrane, causing resistance to the blood flow to the left ventricle. The onset of symptoms depends upon the effective size of the orifice in the membrane and the associated heart disease. Our case is a 67-year-old woman with cor triatriatum found by chance at the onset of myocardial infarction. Read More

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June 2019
4 Reads

Cor triatriatum with Raghib complex in partial atrioventricular septal defect and common atrium: a rare combination.

Gen Thorac Cardiovasc Surg 2020 Jun 27;68(6):641-643. Epub 2019 Jun 27.

Department of Thoracic and Cardiovascular Surgery, Inha University Hospital, 27, Inhang-ro, Jung-gu, Incheon, 22332, South Korea.

Persistent left superior vena cava draining into the left atrium in the absence of coronary sinus and atrial septal defect (Raghib complex) is an uncommon anomaly of systemic venous drainage. We present a unique case of simultaneous presentation of cor triatriatum and persistent left superior vena cava draining into the left atrium in an adult female with partial AV canal and common atrium. Complex intra-atrial baffling including a procedure to redirect flow from a proximal atrial chamber was successful. Read More

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http://dx.doi.org/10.1007/s11748-019-01159-7DOI Listing
June 2020
6 Reads

Cor triatriatum dexter in 17 dogs.

J Vet Cardiol 2019 Jun 30;23:129-141. Epub 2019 Apr 30.

Department of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, 2015 Linden Dr. Madison, WI 53706, USA.

Objectives: The objective of this study was to report the signalment, presentation, clinical and imaging findings, interventions, and outcomes in a group of dogs with cor triatriatum dexter (CTD).

Animals: Seventeen client-owned dogs.

Methods: Medical records were reviewed retrospectively for signalment, history, physical examination findings, imaging and diagnostic findings, presence of concurrent congenital cardiac defects, description of interventional procedures, therapy information, and outcomes. Read More

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http://dx.doi.org/10.1016/j.jvc.2019.03.002DOI Listing
June 2019
8 Reads

Treatment of caudal cavoatrial junction obstruction in a dog with a balloon-expandable biliary stent.

J Vet Cardiol 2019 Jun 28;23:112-121. Epub 2019 Mar 28.

The Heart Center, Nationwide Children's Hospital, 700 Children's Dr., Columbus, OH, 43205, USA.

A 2-year-old intact female mixed breed dog was presented for ascites. Echocardiography demonstrated severe obstruction at the level of the caudal right atrium. Initially, a variant of cor triatriatum dexter was diagnosed, and balloon catheter dilation was performed. Read More

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http://dx.doi.org/10.1016/j.jvc.2019.02.004DOI Listing
June 2019
17 Reads

Cor triatriatum sinistrum diagnosed in the adulthood: a systematic review.

Heart 2019 08 5;105(15):1197-1202. Epub 2019 Jun 5.

Department of Cardiology, Rigshospitalet, Copenhagen, Denmark.

Background: We performed a systematic review of cor triatriatum sinistrum (CTS) diagnosed in adults. The aim of this review was to describe the clinical presentation, natural history and management of this congenital heart disease.

Methods: A PubMed literature search for 'cor triatriatum sinistrum' published since 2005 was performed. Read More

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http://dx.doi.org/10.1136/heartjnl-2019-314714DOI Listing
August 2019
23 Reads

Computed Tomography Angiography and Magnetic Resonance Angiography of Congenital Anomalies of Pulmonary Veins.

J Comput Assist Tomogr 2019 May 6. Epub 2019 May 6.

From the Department of Diagnostic Radiology and.

We aimed to review computed tomography and magnetic resonance angiography of congenital anomalies of pulmonary veins. Total anomalous pulmonary venous return shows all pulmonary veins drain abnormally in another site rather than left atrium. Imaging can detect anomalous veins either supracardiac, infracardiac, or mixed. Read More

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http://dx.doi.org/10.1097/RCT.0000000000000857DOI Listing
May 2019
10 Reads
1.602 Impact Factor

Computed Tomography Angiography and Magnetic Resonance Angiography of Congenital Anomalies of Pulmonary Veins.

J Comput Assist Tomogr 2019 May/Jun;43(3):399-405

From the Department of Diagnostic Radiology and.

We aimed to review computed tomography and magnetic resonance angiography of congenital anomalies of pulmonary veins. Total anomalous pulmonary venous return shows all pulmonary veins drain abnormally in another site rather than left atrium. Imaging can detect anomalous veins either supracardiac, infracardiac, or mixed. Read More

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http://dx.doi.org/10.1097/RCT.0000000000000857DOI Listing
June 2019
8 Reads
1.602 Impact Factor

Left atrial appendage closure in a patient with cor triatriatum.

Eur Heart J Case Rep 2018 Jun 25;2(2):yty072. Epub 2018 Jun 25.

Division of Cardiology, West Virginia University School of Medicine, 1 Medical Drive, Morgantown, WV, USA.

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http://dx.doi.org/10.1093/ehjcr/yty072DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177069PMC
June 2018
5 Reads

Abnormal Pulmonary Venous Drainage With Cor Triatriatum.

Rev Esp Cardiol (Engl Ed) 2019 Apr 29;72(4):341. Epub 2018 Jun 29.

Sección de Imagen, Servicio de Cardiología, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

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http://dx.doi.org/10.1016/j.rec.2018.06.002DOI Listing
April 2019
7 Reads

Cor Triatriatum: A Tale of Two Membranes.

CASE (Phila) 2019 Feb 16;3(1):25-27. Epub 2019 Jan 16.

The Congenital Heart Collaborative, Rainbow Babies and Children's Hospital, Pediatric Cardiology Division, Cleveland, Ohio.

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http://dx.doi.org/10.1016/j.case.2018.08.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6382949PMC
February 2019
17 Reads

Concurrent cor triatriatum sinister and levoatriocardinal vein in an 11-year-old boy presenting with foudroyant pulmonary edema after appendectomy: A living tribute to the mal-incorporation theory.

Anatol J Cardiol 2019 Mar;21(3):172-174

Division of Pediatric Cardiology, Changhua Christian Children's Hospital; Department of Pediatrics, School of Medicine, Kaohsiung Medical University; Kaohsiung-Taiwan.

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http://dx.doi.org/10.14744/AnatolJCardiol.2018.60980DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6457400PMC
March 2019
8 Reads

Long-standing persistent atrial fibrillation ablation without use of fluoroscopy in a patient with cor triatriatum.

HeartRhythm Case Rep 2019 Feb 4;5(2):88-92. Epub 2018 Nov 4.

Virginia Cardiovascular Specialists, Chippenham Hospital, Richmond, Virginia.

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http://dx.doi.org/10.1016/j.hrcr.2018.10.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379490PMC
February 2019
9 Reads

Bidirectional flow across a perforate cor triatriatum dexter in a dog with concurrent pulmonary, tricuspid, and mitral valve dysplasia.

J Vet Cardiol 2019 Feb 25;21:93-97. Epub 2019 Jan 25.

Department of Clinical Sciences, Colorado State University, 300 W Drake Rd., Fort Collins, CO 80523, USA.

A 10-week-old male intact mixed breed dog presented for evaluation of suspected right-sided congestive heart failure. Echocardiographic imaging revealed a perforate cor triatriatum dexter (CTD), along with pulmonary valve stenosis and tricuspid and mitral valve dysplasia. In typical CTD cases, there is unidirectional blood flow across the dividing membrane, from the caudal into the cranial right atrial chambers. Read More

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http://dx.doi.org/10.1016/j.jvc.2018.12.002DOI Listing
February 2019
13 Reads

Cor triatriatum sinister with left anomalous pulmonary venous return to innominate vein.

Cardiol Young 2019 Mar 24;29(3):428-430. Epub 2019 Jan 24.

Department of Cardiac Surgery,University of Heidelberg,Heidelberg,Germany.

Cor triatriatum sinister is a rare congenital abnormality, with varying signs and symptoms related to the anatomic features and the components of the accompanying cardiac abnormalities. We present a 3-year-old girl who underwent successful simultaneous operation with complete loss of the membrane and ligation of vertical vein by anomalous venous return. The principles for surgical management of cor triatriatum can be summarised as radical resection of the membrane and correction of other intracardiac anomalies. Read More

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http://dx.doi.org/10.1017/S1047951118002305DOI Listing
March 2019
10 Reads

Minimally Invasive Periareolar Approach to Cor Triatriatum Repair.

Innovations (Phila) 2018 Nov/Dec;13(6):445-447

From the Division of Cardiac Surgery.

Cor triatriatum sinister is an uncommon cardiac abnormality characterized by a membrane that divides the left atrium into two chambers. Definitive management requires surgical resection, traditionally through sternotomy. Minimally invasive reparative techniques are associated with reduced blood loss, shorter hospitalization, faster recovery time, and improved cosmesis with excellent patient satisfaction. Read More

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http://dx.doi.org/10.1097/IMI.0000000000000565DOI Listing
April 2019
10 Reads

Cor triatriatum dexter with right ventricular hypoplasia: Role of multimodality imaging in decision making.

Echocardiography 2018 12 9;35(12):2113-2116. Epub 2018 Nov 9.

Cleveland Clinic Children's Hospital, Cleveland, Ohio.

Cor Triatriatum Dexter (CTD) is a rare congenital anomaly involving the systemic venous valves. Failure of regression of the right-sided sinus venosus valve leads to abnormal septation of the right atrium and a variety of right atrial and tricuspid valve obstructive lesions. The presentation can be varied ranging from asymptomatic to persistent neonatal cyanosis. Read More

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http://doi.wiley.com/10.1111/echo.14175
Publisher Site
http://dx.doi.org/10.1111/echo.14175DOI Listing
December 2018
43 Reads

Subtotal Cor Triatriatum on Dual-Source Computed Tomography.

Ann Thorac Surg 2019 03 31;107(3):e213. Epub 2018 Oct 31.

Department of Cardiovascular Radiology and Endovascular Interventions, All India Institute of Medical Sciences, New Delhi, India.

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http://dx.doi.org/10.1016/j.athoracsur.2018.09.029DOI Listing
March 2019
9 Reads

Interatrial shunts: technical approaches to percutaneous closure.

Expert Rev Med Devices 2018 10 26;15(10):707-716. Epub 2018 Sep 26.

d Department of Interventional cardiology , Cho-Ray Hospital , Ho Chi minh City , Vietnam.

Introduction: Interatrial shunt closure is considered the first-line therapy for congenital simple communications such as patent forame ovale (PFO), atrial septal defect (ASD), and post surgical interatrial communications.

Areas Covered: Anatomical, functional, and technical details useful for planning a transcatheter-based closure procedure are discussed as well as the available equipments and their use and the procedural routes and the specific closure techniques.

Expert Commentary: Anatomical and functional details, appreciated at both pre-procedural and intraprocedural steps, are of paramount importance for planning interatrial shunts transcatheter - based closure procedures. Read More

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http://dx.doi.org/10.1080/17434440.2018.1526674DOI Listing
October 2018
13 Reads

Agitated saline contrast echocardiography reveals cor triatriatum dexter.

Echocardiography 2018 11 16;35(11):1895-1897. Epub 2018 Sep 16.

Department of Cardiology, King's College Hospital NHS Foundation Trust, King's College London, London, UK.

We present the case of a 54-year-old man who had an unusual finding in contrast echocardiography with agitated saline. Partition of the right atrium in two compartments, an opacified and a non-opacified one, was noted. Further assessment with a transesophageal echocardiogram revealed the presence of a membrane in the right atrium, with the final diagnosis being cor triatriatum dexter. Read More

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http://dx.doi.org/10.1111/echo.14142DOI Listing
November 2018
9 Reads
1.254 Impact Factor

[Cor Triatriatum in an Adult Patient Conbined with Mitral Regurgitation and Coronary Artery Disease;Report of a Case].

Kyobu Geka 2018 Aug;71(8):610-614

Division of Cardiovascular Surgery, Shiga University of Medical Science, Otsu, Japan.

A 71-year-old female, who had been diagnosed with cor triatriatum 30 years before, presented with complains of worsening dyspnea and fatigue. She was diagnosed with a combination of cor triatriatum, mitral valve disease and coronary artery disease. She underwent removal of the left atrial membrane, repair of the mitral valve and coronary artery bypass grafting. Read More

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August 2018
22 Reads

Selective Partial Obstruction of Inferior Vena Cava Blood Flow During Diastole: Cor Triatriatum Dexter, Large Eustachian Valve, or Chiari Network?

J Cardiothorac Vasc Anesth 2019 Feb 29;33(2):575-578. Epub 2018 Jul 29.

Cardiothoracic Surgery Services, Clement J. Zablocki Veterans Affairs Medical Center, Milwaukee, WI.

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https://linkinghub.elsevier.com/retrieve/pii/S10530770183057
Publisher Site
http://dx.doi.org/10.1053/j.jvca.2018.07.038DOI Listing
February 2019
72 Reads

Cor triatriatum sinistrum in a pregnant woman.

Authors:
Taherpour Zhiva

Clin Case Rep 2018 Aug 4;6(8):1624-1626. Epub 2018 Jun 4.

Cardiovascular Diseases Department Kermanshah University of Medical Sciences Kermanshah Iran.

Cor triatriatum sinistrum is a congenital cardiac malformation in which left atrium is divided into 2 parts by a perforated fibromuscular membrane, it can mimic signs and symptoms of mitral valve (MV) stenosis or occasionally without any symptoms and discovered as an accidental finding Read More

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http://doi.wiley.com/10.1002/ccr3.1621
Publisher Site
http://dx.doi.org/10.1002/ccr3.1621DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099034PMC
August 2018
77 Reads

Cor Triatriatum: Case Report of Emergency Department Diagnosis.

Clin Pract Cases Emerg Med 2018 Aug 12;2(3):227-230. Epub 2018 Jun 12.

SUNY Upstate Medical University, Department of Emergency Medicine, Syracuse, New York.

Cor triatriatum is a rare, congenital heart defect. When diagnosis does not occur in infancy, primary symptoms in an older patient may mimic reactive airway disease. We report a case of cor triatriatum in an older child, previously diagnosed with asthma, presenting to an emergency department with a chief complaint of wheezing. Read More

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http://dx.doi.org/10.5811/cpcem.2018.5.37921DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6075497PMC
August 2018
34 Reads

Cor Triatriatum Sinister with Secundum Atrial Septal Defect.

CASE (Phila) 2017 Aug 26;1(4):141-146. Epub 2017 Jul 26.

University Health Network, Toronto General Hospital, Peter Munk Cardiac Centre and Toronto Congenital Cardiac Centre for Adults, and University of Toronto, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1016/j.case.2017.05.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058282PMC
August 2017
14 Reads