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Takayasu Arteritis Presenting As Epileptic Seizure: A Case Report
Ramesh Shrestha1, Abnish Pandit2, Ghanshyam Kharel3
1Internal Medicine, Tribhuvan University/Chitwan Medical College, Kathmandu, NPL.
Takayasu arteritis, a large-vessel vasculitis, rarely presents as epileptic seizures. Prompt treatment with glucocorticoids and immunosuppressants effectively managed the patient's neurological symptoms and inflammation.
Area of Science:
- Cardiology
- Neurology
- Immunology
Background:
- Takayasu arteritis is a rare, chronic inflammatory condition affecting large arteries.
- Its varied presentation and subtle early vascular lesions complicate diagnosis.
- Neurological manifestations, such as epileptic seizures, are infrequent but significant.
Observation:
- A 20-year-old female presented with an unusual neurological episode mimicking epileptic seizures.
- The patient experienced unresponsiveness, tonic stiffening, limb jerks, fatigue, and memory loss.
- This presentation was ultimately attributed to an acute phase of Takayasu arteritis.
Findings:
- The patient received high-dose glucocorticoid and immunosuppressive therapy during the acute phase.
- This treatment successfully controlled the underlying inflammatory process.
- The neurological symptoms resolved, and the patient showed significant clinical improvement.
Implications:
- Highlights the importance of considering vasculitis in atypical neurological presentations.
- Demonstrates the efficacy of aggressive immunosuppressive therapy in managing Takayasu arteritis-related neurological events.
- Emphasizes the need for comprehensive diagnostic evaluation in complex cases.
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