Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

: A rare case of cor triatriatum sinistrum in combination with anomalies in the atrial septum and in the right atrium of a 60-year-old female body donor is described here. : In addition to classical dissection, ultrasound and magnetic resonance imaging, computer tomography and cinematic rendering were performed. In a reference series of 59 regularly formed hearts (33 men, 26 women), we looked for features in the left and right atrium or atrial septum. In addition, we measured the atrial and ventricular wall thickness in 15 regularly formed hearts (7 men, 8 women). : In the case described, the left atrium was partly divided into two chambers by an intra-atrial membrane penetrated by two small openings. The 2.5 cm-high membrane originated in the upper level of the oval fossa and left an opening of about 4 cm in diameter. Apparently, the membrane did not lead to a functionally significant flow obstruction due to the broad intra-atrial communication between the proximal and distal chamber of the left atrium. In concordance with this fact, left atrial wall thickness was not elevated in the cor triatriatum sinistrum when compared with 15 regularly formed hearts. In addition, two further anomalies were found: 1. the oval fossa was deepened and arched in the direction of the left atrium; 2. the right atrium showed a membrane-like structure at its posterior and lateral walls, which began at the lower edge of the oval fossa. It probably corresponds to a strongly developed eustachian valve (valve of the inferior vena cava). : The case described suggests that malformations in the development of the atrial septum and in the regression of the valve of the right sinus vein are involved in the pathogenesis of cor triatriatum sinistrum.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8402230PMC
http://dx.doi.org/10.3390/medicina57080777DOI Listing

Publication Analysis

Top Keywords

cor triatriatum
16
triatriatum sinistrum
16
atrial septum
16
left atrium
16
regularly formed
12
formed hearts
12
oval fossa
12
septum atrium
8
atrium 60-year-old
8
hearts men
8

Similar Publications

Cor triatriatum is a rare congenital heart defect that divides the right or left atrium into three chambers. Although the diagnosis is typically made within the first years of birth, it can occasionally be made later in adulthood and is frequently associated with other cardiac defects but may be present in isolation. Clinical manifestations range from lung congestion, exhaustion, coughing, and dyspnea to the onset of heart failure.

View Article and Find Full Text PDF

Atrioventricular septal defect (AVSD) with cor triatriatum sinister (CTS) is a rare congenital anomalous combination. Few cases of AVSD and CTS have been reported in the literature. However, an isolated case of CTS with partial AVSD, left superior vena cava, and unroofed coronary sinus in an adult has not been reported in the literature.

View Article and Find Full Text PDF

This case study involves a 51-year-old woman with a complex cardiovascular condition, namely cor triatriatum dexter, accompanied by sick sinus syndrome. She presented with bradycardia, dizziness, and amaurosis, and was admitted to the emergency department due to right limb numbness. Diagnostic examinations, including computed tomography and cardiac color ultrasound screening, revealed the presence of cor triatriatum dexter with an enlarged left atrium and ventricle.

View Article and Find Full Text PDF

Cor triatriatum sinister (CTS) is a rare congenital anomaly characterized by a fibromuscular membrane that divides the left atrium into proximal and distal chambers. Typically, the pulmonary veins drain into the proximal chamber, while the distal chamber remains continuous with the left atrial appendage and the mitral valve. Communication between the two chambers occurs through one or more fenestrations of variable size.

View Article and Find Full Text PDF