CC BY-NC-ND 4.0 · International Journal of Epilepsy 2018; 05(02): 107-109
DOI: 10.1055/s-0039-1688528
Case Report
Indian Epilepsy Society

Seizures in Idiopathic Pulmonary Arterial Hypertension

1   Department of Medicine, Federal University of Santa Maria, Santa Maria, Rio Grande do Sul, Brazil
,
Ana Letícia Fornari Caprara
1   Department of Medicine, Federal University of Santa Maria, Santa Maria, Rio Grande do Sul, Brazil
› Author Affiliations
Further Information

Publication History

Received: 13 January 2019

Accepted after revision: 16 March 2019

Publication Date:
16 May 2019 (online)

Abstract

Pulmonary arterial hypertension (PAH) is a progressive pulmonary vasculopathy. A 29-year-old female patient presenting with dyspnea and syncope within 6 hours of onset was admitted to our hospital. The patient stated that she looked for a neurologist months ago because she experienced abrupt shaking limbs occurring during physical activity. She was diagnosed with focal seizure, and carbamazepine (CBZ) was started. On admission, she reported that the dyspnea had started in the last week and recurrent episodes of syncope in the last few hours. A right heart catheterization was diagnostic of PAH. She was started on spironolactone, furosemide, sildenafil, warfarin, and supplemental oxygen. On 10th admission day, the patient was seizure free and the dose of CBZ was tapered. In the follow-up, the patient remained seizure free. An investigation to search for a chronic lung disease or hypoxemia, systemic disorder, hematological disorder, and metabolic disorder was negative.

 
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