| Literature DB >> 23576669 |
Monica Gupta1, Kamal Singh, S S Lehl, Mala Bhalla.
Abstract
Takayasu's arteritis is a rare, systemic vasculitis with varied presentations across multiple medical specialities. Here, we present a young woman who had recurrent episodes of erythema nodosum on the background of a low-grade fever and no vascular manifestations. The presence of a high erythrocyte sedimentation rate generated a high index of suspicion for underlying vasculitis, and radioimaging confirmed the suspicion of Takayasu's arteritis. The patient was found to have type III diseases in the vasculitic stage and was managed with systemic corticosteroids.Entities:
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Year: 2013 PMID: 23576669 PMCID: PMC3645399 DOI: 10.1136/bcr-2013-009507
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X