Cor triatriatum sinister: a case series

2015 ◽  
Author(s):  
Onur Işık
Keyword(s):  
Case Series ◽  
Cor Triatriatum ◽  
Cor Triatriatum Sinister

Catheter Ablation of Atrial Fibrillation in Patients with Cor Triatriatum Sinister; Case Series and Review of Literature

2021 ◽  
Author(s):  
Ahmadreza Karimianpour ◽  
Amanda W. Cai ◽  
Frank A. Cuoco ◽  
J. Lacy Sturdivant ◽  
Sheldon E. Litwin ◽  
...  
Keyword(s):  
Atrial Fibrillation ◽  
Catheter Ablation ◽  
Case Series ◽  
Cor Triatriatum ◽  
Review Of Literature ◽  
Cor Triatriatum Sinister

PP-162 Cor Triatriatum Sinister: A Case Series

2015 ◽  
Vol 115 ◽  
pp. S168
Author(s):  
Onur Isik ◽  
Muhammet Akyuz ◽  
Mehmet Fatih Ayik ◽  
Umit Kahraman ◽  
Ali Onder Kilic ◽  
...  
Keyword(s):  
Case Series ◽  
Cor Triatriatum ◽  
Cor Triatriatum Sinister

scholarly journals Cor triatriatum – Uma Revisão de Literatura

2017 ◽  
Vol 4 (1) ◽  
pp. 110
Author(s):  
Camila Carneiro Araujo ◽  
Ercília Maria Carvalho ◽  
Amanda Luiza Nascimento ◽  
Sheila Sousa Santos ◽  
Paula Priscila Correia
Keyword(s):  
Cor Triatriatum ◽  
Insuficiencia Cardiaca ◽  
Cor Triatriatum Sinister ◽  
Cor Triatriatum Dexter

O Cor triatriatum é uma anomalia congênita de ocorrência rara em cães. Nesta, identifica-se a presença de três átrios no coração, sendo denominado Cor triatriatum dexter quando há um átrio a mais do lado direito e Cor triatriatum sinister quando esta anomalia ocorre do lado esquerdo. A causa da doença ainda não está conhecida, mas é sabido que ocorre falhas na embriogênese do animal acometido por esta enfermidade. Os animais que possuem a doença apresentam sinais de insuficiência cardíaca direita ou esquerda. O diagnóstico é realizado por meio de exames complementares, dentre estes, se destaca o ecodopplercardiograma como método de escolha. O tratamento baseia-se na correção cirúrgica e/ou tratamento para a insuficiência cardíaca. Para evitar o surgimento desta anomalia, recomenda-se a castração destes animais, a não repetição do cruzamento que gerou este filhote, assim como, cruzamento consanguíneos.

Surgical Treatment of Cor Triatriatum Sinister in a Cat Under Cardiopulmonary Bypass

2015 ◽  
Vol 44 (8) ◽  
pp. 964-969 ◽  
Author(s):  
Nicolas Borenstein ◽  
Vassiliki Gouni ◽  
Luc Behr ◽  
Emilie Trehiou-Sechi ◽  
Amandine Petit ◽  
...  
Keyword(s):  
Cardiopulmonary Bypass ◽  
Surgical Treatment ◽  
Cor Triatriatum ◽  
Cor Triatriatum Sinister

scholarly journals Isolated Cor Triatriatum Sinister: A Case Report

2020 ◽  
Vol 18 (1) ◽  
pp. 28-30
Author(s):  
Zanda Grīnberga ◽  
Pauls Sīlis ◽  
Elīna Ligere ◽  
Ingūna Lubaua ◽  
Inta Bergmane ◽  
...  
Keyword(s):  
Left Atrium ◽  
Pulmonary Veins ◽  
Surgical Excision ◽  
Venous Drainage ◽  
Treatment Method ◽  
Cor Triatriatum ◽  
Cardiac Anomaly ◽  
Congenital Cardiac Anomaly ◽  
Cor Triatriatum Sinister ◽  
The Right

SummaryCor triatriatum sinister is a rare congenital cardiac anomaly that has been identified in 0.1% of children with congenital heart disease. It is defined as a fibromuscular membrane that divides the left atrium into two chambers: a superior (proximal) that in most cases receives drainage from the pulmonary veins and an inferior (distal) chamber that communicates with the mitral valve and the left atrium. Cor triatriatum sinister can be an isolated lesion (approximately 25% of cases), but in many cases it is associated with other congenital cardiovascular anomalies, the most common one being – atrial septal defect(3). Symptoms in patients with cor triatriatum sinister are related to obstruction of pulmonary venous drainage, pressure loading of the right side of the heart and congestive cardiac failure. Depending on the severity of the obstruction and presence of associated cardiac anomalies it can be diagnosed at any age. Diagnosis is usually achieved by echocardiography in early infancy. Elective treatment method is surgical excision of the membrane. Here we present a pediatric patient (4 months old) presenting in cardiogenic shock with a successful correction of isolated cor triatriatum sinister. To confirm diagnosis and success of surgical repair, transthoracic and transesophageal echocardiography were used.

scholarly journals Cor Triatriatum Sinister in a 25 Year Old Patient - A Case Report

2020 ◽  
Vol 2020 ◽  
Author(s):  
Ketak Nagare
Keyword(s):  
Balloon Dilatation ◽  
Cor Triatriatum ◽  
Cardiac Anomaly ◽  
Early Age ◽  
Corrective Surgery ◽  
Emergency Case ◽  
Adult Age ◽  
Congenital Cardiac Anomaly ◽  
Choice Of Treatment ◽  
Cor Triatriatum Sinister

Cor triatriatum sinister is a rare congenital cardiac anomaly in which a fibromuscular membrane divides the left atria into 2 chambers. It is even rarer when present at an adult age. Symptoms and presentation of the patient depend on the size of the opening into the membrane through which 2 chambers of left atrium communicate with each other. Cor triatriatum sinister rarely remains asymptomatic till adulthood. In adults symptoms of Cor triatriatum sinister mimic the symptoms of mitral stenosis. Corrective surgery is the choice of treatment, but when it present as an emergency case especially at an early age, balloon dilatation of the membrane opening is done. Elective balloon dilatation of membrane opening at an early age diagnosed with Cor triatriatum sinister followed by corrective surgery at an adult age can be a safer option compared to direct corrective surgery at an early age.  We present a case of a 25-year-old female who was diagnosed first time at this age as cor triatriatum sinister and treated successfully with corrective surgery.

scholarly journals Partial atrioventricular canal defect with cor triatriatum sinister: report of three cases

2004 ◽  
Vol 127 (2) ◽  
pp. 572-573 ◽  
Author(s):  
Praveen K. Varma ◽  
Girish Warrier ◽  
Padmakumar Ramachandran ◽  
Praveen Kumar Neema ◽  
Soman Rema Krishna Manohar ◽  
...  
Keyword(s):  
Cor Triatriatum ◽  
Atrioventricular Canal ◽  
Atrioventricular Canal Defect ◽  
Cor Triatriatum Sinister
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