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Eosinophilic fasciitis: an atypical presentation of a rare disease

dc.contributor.authorCabral, C
dc.contributor.authorNovais, A
dc.contributor.authorAraujo, D
dc.contributor.authorMosca, A
dc.contributor.authorLages, A
dc.contributor.authorKnock, A
dc.date.accessioned2019-05-16T13:16:26Z
dc.date.available2019-05-16T13:16:26Z
dc.date.issued2019-03
dc.description.abstractEosinophilic fasciitis, or Shulman's disease, is a rare disease of unknown etiology. It is characterized by peripheral eosinophilia, hypergammaglobulinemia, and high erythrocyte sedimentation rate. The diagnosis is confirmed by a deep biopsy of the skin. The first line of treatment is corticotherapy. We present a rare case of eosinophilic fasciitis in a 27-year-old woman with an atypical presentation with symmetrical peripheral edema and a Groove sign. The patient responded well to treatment with corticosteroids at high doses and, in this context, was associated with hydroxychloroquine and azathioprine. After two and a half years, peripheral eosinophilia had increased, and more of her skin had hardened. At that time, the therapy was modified to include corticoids, methotrexate, and penicillamine. It is of great importance to publicize these cases that allow us to gather experience and better treat our patients.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationRev Assoc Med Bras (1992). 2019 Mar;65(3):326-329.pt_PT
dc.identifier.doi10.1590/1806-9282.65.3.326pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.23/1328
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.subjectFasceíte Eosinofílicapt_PT
dc.titleEosinophilic fasciitis: an atypical presentation of a rare diseasept_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage329pt_PT
oaire.citation.issue3pt_PT
oaire.citation.startPage326-329pt_PT
oaire.citation.volume65pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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