Terson syndrome in a patient with unrepaired tetralogy of Fallot

Amina Saddiqa; Zaid Waqar; Maryam Khalil; Muhammad Anas; Zeeshan Munawar; Ifrah Ayaz; zakir Jan; Haris Majid

doi:10.56310/pjns.v18i02.229

Amina Saddiqa Department of Neurology, Pakistan Institute of Medical Sciences, Islamabad
Zaid Waqar Department of Neurology, Pakistan Institute of Medical Sciences, Islamabad
Maryam Khalil Department of Neurology, Pakistan Institute of Medical Sciences, Islamabad
Muhammad Anas Department of Neurology, Pakistan Institute of Medical Sciences, Islamabad
Zeeshan Munawar Department of Neurology, Pakistan Institute of Medical Sciences, Islamabad
Ifrah Ayaz Department of Neurology, Pakistan Institute of Medical Sciences, Islamabad
zakir Jan Department of Neurology, Pakistan Institute of Medical Sciences, Islamabad
Haris Majid Department of Neurology, Pakistan Institute of Medical Sciences, Islamabad

DOI: https://doi.org/10.56310/pjns.v18i02.229

Keywords: Tetralogy of Fallot, Ventricular septal defect, Terson syndrome

Abstract

Tetralogy of Fallot is the most commonly seen cyanotic congenital heart disease. It includes four cardinal features: right ventricular outflow tract obstruction, misaligned ventricular septal defect, overriding aorta, and concentric right ventricular hypertrophy. Intracranial pathologies such as brain abscesses, cerebrovascular accidents, and intracranial haemorrhage all have been reported with Tetralogy of Fallot. Here we present a case who had subarachnoid haemorrhage with vitreous haemorrhage in Tetralogy of Fallot.