| Literature DB >> 32967943 |
Atanu Chandra1, Swarup Kanta Saha2, Aritra Kumar Ray2, Parthasarathi Karmakar2.
Abstract
Rowell's syndrome is a rare disorder characterised by an association of lupus erythematosus with erythema multiforme (EM)-like skin lesions. EM as the initial clinical presentation of systemic lupus erythematosus is also atypical and even rarer. We report the case of an 18-year-old girl admitted to our hospital with fever and polyarthralgia along with multiple discrete ill-defined target lesions with crust formation over forehead, cheek, external ears, scalp, upper chest and back (predominantly over sun-exposed areas) with ulceration over hard palate. Investigations revealed pancytopaenia, a positive rheumatoid factor, positive antinuclear antibody with a speckled pattern, anti-Smith antibody and strongly positive anti-Ro. Patient was diagnosed with Rowell's syndrome as per clinical and laboratory features. Majority of skin lesions including oral ulcerations subsided gradually after treatment with steroids and hydroxychloroquine. © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: dermatology; rheumatology; systemic lupus erythematosus
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Year: 2020 PMID: 32967943 PMCID: PMC7513572 DOI: 10.1136/bcr-2020-235173
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X