Subtotal cor triatriatum with left partial anomalous pulmonary venous return

Jennings, Rufus B.; Innes, Bruce J.

doi:10.1016/s0022-5223(19)41363-9

Cited by 13 publications

(5 citation statements)

References 16 publications

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“…The basic surgical management for CTS is the resection of the fibromuscular membrane inside the LA, accompanied if necessarily by surgical intervention for concomitant cardiac malformations. In CTS associated with left anomalous pulmonary venous drainage, the necessity of surgical intervention on the VV varies among patients depending on anatomical and hemodynamic evaluation [3][4][5][6][7].…”

Section: Discussionmentioning

confidence: 99%

“…The first successful surgical repair of CTS associated with left PAPVR was reported in 1977 by Jennings et al [ 5 ]. Their patient was a 10-week-old infant with an obstructive subtotal cor triatriatum with left PAPVR (Lucas–Schmidt classification III A2).…”

Section: Discussionmentioning

confidence: 99%

“…Cor triatriatum sinister (CTS) represents only 0.1% of all cardiac malformations [1]. Partial or total anomalous pulmonary venous return (PAPVR/TAPVR) is reported as a coexisting disease in 10-33% of patients with CTS [2], but left anomalous pulmonary venous drainage coexisting with CTS is less frequently described [3][4][5][6][7]. CTS with left anomalous pulmonary venous drainage may be hemodynamically similar to obstructive TAPVR when a common pulmonary venous collector (CPVC) is present, and surgical intervention may be urgently needed [3].…”

Section: Introductionmentioning

confidence: 99%

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Cor triatriatum sinister with left anomalous pulmonary venous drainage to innominate vein: what to do with the vertical vein?

Ishiwari

Nomura

Hamaya

et al. 2020

Gen Thorac Cardiovasc Surg

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We treated a surgical case of a 47-day-old male infant diagnosed with an unusual type of cor triatriatum sinister (CTS) with left anomalous pulmonary venous drainage to the innominate vein via a vertical vein. After preoperative hemodynamic assessment of pulmonary venous (PV) return, this patient underwent a resection of the fibromuscular membrane between the accessory and the true left atrial chambers, concomitant with vertical vein banding to facilitate a left PV return through a common pulmonary venous collector (CPVC). Catheterization three months after this surgery revealed no obstruction of the PV return to the mitral orifice as well as good growth of the CPVC as a left PV return pathway. The patient has been doing well on aspirin.

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Section: Discussionmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

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Cor triatriatum sinister with left anomalous pulmonary venous drainage to innominate vein: what to do with the vertical vein?

Ishiwari

Nomura

Hamaya

et al. 2020

Gen Thorac Cardiovasc Surg

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“…Later in 1905, Borst gave the name cor-triatriatum [6]. In children, it may be associated with other major congenital cardiac anomalies such as tetralogy of Fallot, double outlet right ventricle, coarctation of the aorta, partial anomalous pulmonary venous connection, persistent left superior vena cava to coronary sinus, ventricular septal defect, atrioventricular septal defect, and common atrioventricular canal [7]. Left superior vena cava is more frequently associated when compared to other anomalies [8].…”

Section: Introductionmentioning

confidence: 99%

Cor-Triatriatum Mimicry: Dilated Coronary Sinus Draining the Left Superior Vena Cava in Focus

Anusha,

Gopal

2023

JCR

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Background: Cor-triatriatum is a rare congenital cardiac abnormality in which left atrium (sinister) or the right atrium (dextrum) is divided into two compartments by a fold of tissue or a fibromuscular membrane. Left superior vena cava (LSVC) is more frequently associated when compared to other anomalies. Due to the rarity of the condition, a high index of suspicion is need to prevent unfavourable outcomes. Case Report: We report a case of 11-year-old male having complaints of exertional dyspnea for 2 months, who underwent surgery for cor-triatriatum. But the membrane was formed by persistent left superior vena cava with dilated coronary sinus which was closely mimicking cortriatriatum. Conclusion: This case emphasizes about the complexities associated with persistent LSVC, especially in the context of mimicking other congenital cardiac abnormalities.

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“…6 Cor triatriatum, a heart with 3 atria (triatrial heart), is a congenital anomaly in which the left atrium (cor triatriatum sinistrum) or right atrium (cor triatriatum dextrum) is divided into 2 parts by a fold of tissue, a membrane, or a fibromuscular band. 7 However, variable types of subtotal cor triatriatum are also noted, with only the right or left pulmonary veins draining into the upper chamber. 8…”

Section: Introductionmentioning

confidence: 99%

A Five (5) chamber heart (Cor Triatriatum) in Infancy: A rare congenital heart defect

et al. 2013

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Five-chambered heart is extremely rare in children. We report a case of asymptomatic five chamber heart detected in infancy. The patient is 2-day-old and managed in a special care baby unit (SCBU) for neonatal sepsis. During routine follow-up at the age of 1 month, she was found to have an asymptomatic murmur. Echocardiograph reported five-chambered heart, concluding that it is Cor triatriatum, supravalvular pulmonary stenosis and secundum atrial septal defect. The child is still been followed-up and is still asymptomatic at 7 months. Five-chambered heart, although rare, can occur even if asymptomatic.

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Subtotal cor triatriatum with left partial anomalous pulmonary venous return

Cited by 13 publications

References 16 publications

Cor triatriatum sinister with left anomalous pulmonary venous drainage to innominate vein: what to do with the vertical vein?

Cor triatriatum sinister with left anomalous pulmonary venous drainage to innominate vein: what to do with the vertical vein?

Cor-Triatriatum Mimicry: Dilated Coronary Sinus Draining the Left Superior Vena Cava in Focus

A Five (5) chamber heart (Cor Triatriatum) in Infancy: A rare congenital heart defect

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