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Published on: October 20, 2017
Late presentation of TAPVC with multiple cerebral abscesses
Kushal Naha1, G Vivek, Ranjan K Shetty
1Department of Medicine, Kasturba Medical College, Manipal, Karnataka, India.
A rare case of adult-onset cyanotic congenital heart disease, specifically total anomalous pulmonary venous connection (TAPVC), presented unusually with cerebral abscesses. This highlights a less common pathway for TAPVC diagnosis in adults.
Area of Science:
- Cardiology
- Neurology
- Pediatric Cardiology
Background:
- Congenital heart disease (CHD) often presents in infancy or childhood.
- Total anomalous pulmonary venous connection (TAPVC) is a rare cyanotic CHD where pulmonary veins do not connect normally to the left atrium.
- Adult presentation of TAPVC is uncommon, with varied clinical manifestations.
Observation:
- A 24-year-old male presented with acute neurological symptoms: fever, headache, vomiting, and seizures.
- Initial diagnostic workup revealed cerebral abscesses as the primary clinical issue.
- Further cardiac evaluation identified non-obstructive supracardiac TAPVC as the underlying etiology.
Findings:
- The patient had no prior history of cardiac symptoms, making the adult diagnosis of TAPVC unexpected.
- Cerebral abscesses are an unusual primary manifestation of TAPVC.
- This case underscores the potential for severe, atypical presentations of CHD in adulthood.
Implications:
- Highlights the importance of considering congenital heart disease in adults presenting with unexplained neurological deficits.
- Suggests that TAPVC, though rare, can manifest late in life with severe complications.
- Emphasizes the need for comprehensive diagnostic approaches in complex adult cases.
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