| Literature DB >> 20416987 |
H Wastiaux1, B Hervier, C Durant, V Gagey-Caron, A Masseau, S Barbarot, M Hamidou.
Abstract
Relapsing polychondritis (RP) is a rare disorder characterized by recurrent inflammatory episodes involving various cartilages. The clinical course of RP is variable, and dermatologic manifestations are uncommon. We report a 73-year-old patient who presented with a neutrophilic dermatosis (Sweet's syndrome) as the initial manifestation of RP. There was no evidence for a myelodysplastic syndrome, as it has been previously reported with RP, but the patient was followed-up for an indolent and untreated chronic lymphocytic leukaemia. Complete remission was obtained with oral corticosteroids. This report highlights the clinical spectrum of the RP. Copyright 2010 Société nationale française de médecine interne (SNFMI). Published by Elsevier SAS. All rights reserved.Entities:
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Year: 2010 PMID: 20416987 DOI: 10.1016/j.revmed.2009.05.013
Source DB: PubMed Journal: Rev Med Interne ISSN: 0248-8663 Impact factor: 0.728