Author/Authors :
Almousa ، Samaher Rheumatology and Clinical Immunology Department - Tishreen Hospital - MSA.Research Center , Muhamad ، Ritta Rheumatology and Clinical Immunology Department - Tishreen Hospital - MSA.Research Center , Salameh ، Farah Neurology Department - Tishreen Hospital - MSA.Research Center , Alahmad ، Abdallah Gastrointestinal Department - Tishreen Hospital - MSA.Research Center , Kasem ، Bana Gastrointestinal Department - Tishreen Hospital - MSA.Research Center , Wannous ، Hala Rheumatology and Clinical Immunology Department - Tishreen Hospital - MSA.Research Center
Abstract :
Polyarteritis nodosa (PAN) is a rare inflammatory necrotizing vasculitis with variable clinical manifestations and unusual presentations. Therefore, delays in diagnosis are common. The most common features are polyneuropathy, gastrointestinal, and constitutional symptoms. Central nervous system (CNS) involvement is rare in this disease, manifesting as encephalopathy, headache, seizures, and stroke. However, stroke can be ischemic or hemorrhagic, and it is extremely rare as an initial manifestation of PAN. Here, we present a 67-year-old male patient who presented with an initial stroke. He was diagnosed with PAN when he developed severe multi-system complications leading to death. We aim to increase awareness about this disabling complication of PAN and highlight the importance of considering vasculitis, especially PAN, in the differential diagnosis of ischemic stroke. Early diagnosis and timely treatment can improve clinical outcomes and decrease mortality rates.
Keywords :
Polyarteritis nodosa , PAN , Ischemic stroke , Systemic vasculitis