Unmasking Sturge-Weber Syndrome: A Challenging Case of Refractory Seizures, Facial Angiomas, and Glaucoma in a Young Patient
Abstract
Sturge-Weber Syndrome (SWS) is a rare congenital neurocutaneous disorder associated with a port-wine stain, leptomeningeal angioma, and glaucoma. Here, we present a case of a 16-year-old boy with classical SWS who had a history of seizures since 6 months of age, intellectual disability, and glaucoma. Imaging revealed prominent leptomeningeal enhancement affecting the right temporal and occipital. The patient received intravenous anti-epileptic medication, antibiotics, and regular follow-up was scheduled. Early detection and treatment are critical to prevent ophthalmic and cerebral complications. The management of SWS requires a multidisciplinary approach.
How to Cite This Article
Rehman SU, Shah A, Rashid M, Saeed K, Ali S. Unmasking Sturge-Weber Syndrome: A Challenging Case of Refractory Seizures, Facial Angiomas, and Glaucoma in a Young Patient. J Pak Soc Intern Med. 2025;6(2):194–196. doi:10.70302/jpsim.v6i2.2537
Conflict of Interest
All authors declare no competing interests.
Funding
No specific funding was received for this research.
Funder information follows the Crossref Funder Registry standard.
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