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Published on: April 21, 2017
Perinatal Stroke and Cor Triatriatum Sinister: A Case Report
Inês Mazeda1, Marisa Rodrigues2, Jorge Moreira2
1Pediatrics and Neonatology, Unidade Local de Saúde Póvoa de Varzim/Vila do Conde, Póvoa de Varzim, PRT.
Insights
Cor triatriatum sinister (CTS), a rare congenital heart defect, may be linked to cryptogenic perinatal strokes. Early intervention in such cases can lead to favorable neurodevelopmental outcomes.
Area of Science:
- Pediatric Cardiology
- Neurology
- Congenital Heart Defects
Background:
- Cor triatriatum sinister (CTS) is a rare congenital heart defect involving left atrial division.
- CTS, even in incomplete forms, is associated with thromboembolic events.
- Perinatal stroke is a significant cause of neurological deficits in children.
Abstract:
Cor triatriatum sinister (CTS) is a rare congenital heart defect characterized by a fibromuscular membrane dividing the left atrium. Though often asymptomatic in incomplete forms, CTS has been associated with thromboembolic events. We describe a case of a female child with a history of perinatal stroke presenting with right hemiparesis. Prenatal imaging suggested lateral ventricle asymmetry and localized hemorrhage. Postnatal development was mostly normal until gait abnormalities emerged at 18 months. Neuroimaging confirmed left-sided brain injury consistent with a past vascular insult. Cardiac evaluation revealed non-obstructive CTS with no signs of hemodynamic compromise. Although a direct causal relationship could not be confirmed, the identification of CTS in a cryptogenic perinatal stroke case raises the possibility that subtle atrial anomalies may contribute to fetal thromboembolic events. This case reinforces the importance of comprehensive cardiac evaluation in perinatal strokes and illustrates a favorable neurodevelopmental outcome with early multidisciplinary intervention.
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