vasculitis/epileptische aanval

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Amyloid β-Related Central Nervous System Angiitis Presenting With an Isolated Seizure.

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Amyloid beta-related angiitis (ABRA) of the central nervous system (CNS) is a very rare inflammatory disorder that causes destruction of CNS arteries and subsequent neuronal injury. Most patients with ABRA are old and present with cognitive dysfunction and stroke; however, some patients may present

Partial Seizures as the First Manifestation of Primary Angiitis of the Central Nervous System.

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A young woman presented with initial epileptic seizures and multiple 'mass-like' lesions seen on computed tomography and magnetic resonance imaging. Given this presentation and her past medical history, a cerebral biopsy was performed to rule out malignancy, but showed a necrotizing

Systemic lupus erythematosus presenting with leukocytoclastic vasculitis and seizure during pregnancy.

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Systemic lupus erythematosus (SLE) is a rare multisystem disease with a wide array of presentation and is a diagnostic challenge during pregnancy. A 20-year-old gravida 1 at 39 weeks' gestation was referred to our hospital for elevated blood pressure, headache, and history of seizure. She was

Rheumatoid disease of the CNS with meningeal vasculitis presenting with a seizure.

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[Tetanic convulsions in vasculitis].

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Amyloid β-Related Angiitis of the Central Nervous System Presenting with Seizures and Cognitive Deficit.

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[Amyloid β-related angiitis as rare cause of a generalized convulsive seizure].

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Ulcerative colitis, status epilepticus and intractable temporal seizures.

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Three patients with ulcerative colitis (UC) and without any other risk factors, developed intractable status epilepticus de novo. Intractable temporal lobe seizures followed and were investigated 7-19 years later. Two had bi-temporal abnormalities and catastrophic memory loss and the third, severe

[Periarteriitis nodosa in children and mucocutaneous lymph node syndrome as causes of multifocal convulsions (propulsive petit-mal) (author's transl)].

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On an infant with the classical signs of Kawasaki-disease (MLNS), in whom after a few days began to show distal demarcations on all four extremities due to arterial malperfusion. Parts of these extremities had to be resected. Histologic evaluation showed an infantile type of periarteriitis nodosa.

Wegener's granulomatosis presenting as a primary seizure disorder with brain lesions demonstrated by magnetic resonance imaging.

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Since the earliest attempt by Klinger in 1931 to describe the systemic vasculitis subsequently characterized in 1936 by Wegener as Wegener's granulomatosis, this disorder has been reported to present in a number of differing fashions. No previous description relates Wegener's presenting as a seizure

Central nervous system vasculitis in pediatric microscopic polyangiitis.

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Microscopic polyangiitis is a small vessel vasculitis, associated with myeloperoxidaseantineutrophil cytoplasmic antibody. It rarely occurs in children. Central nervous system involvement in pediatric microscopic polyangiitis is not a well known entity with perhaps only five cases till date. We

Plasma concentrations of complement-activation complexes correlate with disease activity in patients diagnosed with isolated central nervous system vasculitis.

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Isolated central nervous system (CNS) vasculitis is rare medium- sized vessel disease limited to intracerebral vessels. The two most common symptoms of this inflammatory disorder observed at entry to a hospital are headaches and mild memory deficits. Further progression of this disease may result in

Cerebral vasculitis in Henoch-Schönlein purpura: a case report with sequential magnetic resonance imaging changes and treated with plasmapheresis alone.

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Neurological complications are rare during the course of Henoch-Schönlein purpura (HSP). We report a 7-year-old girl with HSP who presented with seizures, loss of vision and disturbance of consciousness. Magnetic resonance imaging (MRI) showed high signal intensity in the gray and white matter over

Cerebral and oculorhinal manifestations of a limited form of Wegener's granulomatosis with c-ANCA-associated vasculitis.

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The authors report on cerebral and oculorhinal manifestations in a patient with a cytoplasmic pattern of antineutrophil cytoplasmic autoantibody (c-ANCA)-associated vasculitis. Recurrent Tolosa-Hunt syndrome, cavernous sinus syndrome, Raeder's paratrigeminal neuralgia, and seizures were the major

Primary angiitis of the central nervous system: a case report.

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Primary angiitis of the central nervous system is a rare and difficult entity. Here we represented the clinical and pathological features of a patient with little response to steroid before definite diagnosis. The 50-year-old male had a fluctuating disease course for more than 3 years. He presented

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