We present a series of 14 Saudi patients diagnosed to have adult-onset Still's disease (AOSD). The clinical and laboratory pattern of AOSD in our series is more or less similar to that in other reported series, apart from having lower cardiac and pulmonary involvement than western series. The disease course was relatively benign, with only half the cases showing recurrences, which were controlled by alterations in the dosage of corticosteroid and NSAIDs. A comparison with other series is given.

Primary Angiitis of the central nervous system is a rare and poorly understood variant of vasculitis. We narrate a case of a 46-year-old male who presented with new onset refractory status epilepticus mimicking autoimmune encephalitis. In this case we are reporting clues that could be useful for diagnosis and extensive literature review on the topic.

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