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Stroke in sickle cell disease in Africa: case report
1Department of Internal Medicine, Muhimbili University College of Health Sciences, P. O. Box 65001, Dar es Salaam, Tanzania.
Insights
Stroke is a major complication in sickle cell disease (SCD), affecting 10-25% of patients. Early identification and intervention strategies, like transcranial doppler ultrasonography, are crucial for managing stroke risk in SCD.
Area of Science:
- Neurology
- Hematology
- Pediatrics
Background:
- Sickle cell disease (SCD) is associated with a high incidence of stroke, a leading cause of morbidity and mortality.
- Cerebral stenosis, particularly involving the circle of Willis, is a primary mechanism for stroke in pediatric SCD patients.
Observation:
- A case report details a child with SCD experiencing cortical blindness and right-sided hemiplegia.
- Brain imaging confirmed a left parietal and occipital lobe infarct.
Findings:
- Stroke in SCD is multifactorial, necessitating identification of high-risk individuals.
- Transcranial doppler ultrasonography is a valuable tool for risk stratification.
- Effective primary and secondary intervention strategies exist for SCD-related stroke.
Implications:
- Current findings underscore the need to integrate established stroke prevention strategies into SCD management guidelines.
- Further research is required to inform healthcare policy and optimize patient care for stroke in SCD.
Abstract:
Stroke, including asymptomatic cerebrovascular events, is a significant cause of morbidity and mortality in sickle cell disease, occurring with an incidence of 10 to 25%. Extensive research has established that cerebral stenosis, involving the circle of Willis, is the most common mechanism in children. We report a child with sickle cell disease who presented with cortical blindness and right-sided hemiplegia. Computerised tomography of the brain revealed an infarct involving the left parietal region and extending to the occipital region. Stroke in SCD is multifactorial, but high-risk individuals can be identified by simple well-established strategies such as transcranial doppler ultrasonography. There are approaches for both primary and secondary interventions, which have been shown to be effective and need to be incorporated into management guidelines for SCD patients. Before schemes are recommended into health care policies, research in the appropriate setting is required.
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