Complex Migraine Case: Unmasking Type 3 Sturge-Weber Syndrome

Research Summary

A recent case study published in Cureus highlights the complexities of diagnosing type 3 Sturge-Weber syndrome, a rare congenital disorder. This syndrome often presents without the skin features typical of other types, making diagnosis challenging. The study details a 30-year-old man with recurrent focal seizures and migraine-like headaches. His symptoms included aura, right-sided weakness, and photophobia, initially misattributed to epilepsy alone. Neuroimaging confirmed type 3 Sturge-Weber syndrome with leptomeningeal angiomas in the left parietal region. The patient also had undiagnosed diabetes, hinting at a potential metabolic link. Treatment with antiepileptic drugs and glycemic control brought clinical improvement, underscoring the need for early neuroimaging in such cases.

Study Details

📄 Title: Type 3 Sturge-Weber Syndrome Presenting With Concurrent Epilepsy and Migraine.

👥 Research Team: Cheema ZZ et al.

📚 Published In: Cureus

📅 Publication Date: 2025 Nov

⚕️ Medical Disclaimer: This summary is generated automatically from recent migraine research. Always consult with healthcare professionals for medical advice.