Skip to content
Research Article Open access CC BY 4.0

Orbital Cellulitis Revealing Sturge-weber Syndrome: A Case Report

Chaimae Aoussar, Sanae Azitoune, Chaimae Nahi, Mohamed Amine Ichane, Khadija Mouadine, Bouchra Chkirate

Asian Journal of Pediatric Research · pp. 35–39 · Published 1 Apr 2024

10.9734/ajpr/2024/v14i4339

Abstract

Sturge-Weber syndrome (SWS), also known as encephalofacial angiomatosis, is a rare congenital neurocutaneous and ocular condition. It is characterized by two types of malformations: a congenital facial port-wine stain and a capillary-venous leptomeningeal angioma, typically homolaterally located, often in the parieto-occipital region. The diagnosis of SWS largely relies on neuroimaging, particularly magnetic resonance imaging (MRI), which is crucial for identifying anomalies before the onset of neuro-ocular complications. We present the case of a child in whom SWS is suspected due to the presence of a facial and leptomeningeal angioma.

Sturge-weber syndrome CT scan encephalofacial angiomatosis angioma

Cited by 0

No indexed citations yet.

Article metrics

Real usage data collected on this platform.

0

Page views

0

PDF downloads

0

Outbound clicks

0

Citations

Views by country

Approximate, from request IP at view time — not citizenship or institution. Countries with fewer than 5 views are grouped as "Other".

No views recorded yet.

Traffic sources

Referring site, by host.

No traffic recorded yet.

Views and downloads exclude known bots/crawlers. Citations combines this platform's own DOI-resolved index with each external source's own reported total — see Cited by above for individually listed citing works. Last refreshed 0 seconds ago.