Fortuitious Diagnosis of Scimitar Syndrome in an Asymptomatic Adult

Scimitar syndrome is a rare congenital anomaly seen as one of the components of congenital pulmonary venolobar syndrome. Simple and traditional investigation tools like CXR if interpreted with vigil can aid in prompt diagnosis and management of patients even in absence of clinical symptoms.

Percutaneous treatment of a double-drainage scimitar-like syndrome

Scimitar syndrome is a rare variant of anomalous right pulmonary vein connection to the inferior vena cava and it is associated with other cardiopulmonary anomalies. It generally requires surgery and sometimes it may go unrecognised into adulthood. We report a unique case of a scimitar syndrome variant in a young adult, who was successfully treated percutaneously, after the first misdiagnosis of arrhythmogenic ventricular cardiomyopathy. The cardiac magnetic resonance unveiled the uncommon anatomical pattern, avoiding surgical repair. Cross-sectional imaging is extremely useful in the diagnosis and treatment planning of CHD in adults.

Congenital Pulmonary Venolobar Syndrome: Neurodevelopmental Follow-up

Congenital pulmonary venolobar syndrome or infantile scimitar syndrome is a rare congenital cardiopulmonary anomaly and has variable presentation, especially in the neonatal period. It is characterized by partial or total anomalous pulmonary venous return from the right lung along with pulmonary hypoplasia. The infantile form is associated with significant mortality and has a worse prognosis due to severe respiratory insufficiency, cardiac failure, and pulmonary infections. We report an infantile scimitar syndrome diagnosed within few hours of life, which has been followed up for 4 years for the presence of intact survival and without neurodevelopmental disorder in the domains of motor, cognition, communication, personal-social, vision, and hearing.