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Drug Reaction With Eosinophilia and Systemic Symptoms Syndrome in a Patient Taking Lamotrigine

dc.contributor.authorLameiras, C
dc.contributor.authorOrnelas, E
dc.contributor.authorLopes, M
dc.contributor.authorDória, MC
dc.date.accessioned2019-12-10T15:26:21Z
dc.date.available2019-12-10T15:26:21Z
dc.date.issued2019
dc.description.abstractDrug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is a rare adverse drug reaction characterised by skin eruption and multiple organ involvement. Diagnosing this entity is challenging due to the variability of clinical manifestations, late onset and relapse even after stopping the causative drug. It is potentially life-threatening; thus, it must be promptly recognised and the causative drug withdrawn. We describe a case of a 50-year-old man with an acute diffuse rash, fever and eosinophilia 4 weeks after having started lamotrigine. The suspected eliciting drug was suspended and systemic corticoid treatment was initiated (prednisolone 0.5 mg/kg/day). Symptoms relapsed under corticoid tapering with greater severity. The patient developed an exuberant rash associated with peripheral lymphadenopathies, marked eosinophilia and hepatic cytolysis. The diagnosis of DRESS syndrome to lamotrigine was made. Prednisolone dosage was increased to 1 mg/kg/day, and the subsequent taper was performed slowly over the course of 10 weeks. Full clinical remission was observed.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationBMJ Case Rep,12 (10) 2019 Oct 25pt_PT
dc.identifier.doi10.1136/bcr-2019-229180pt_PT
dc.identifier.issn1757-790X
dc.identifier.urihttp://hdl.handle.net/10400.10/2341
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherBMJ Pub. Grouppt_PT
dc.subjectEosinophiliapt_PT
dc.subjectDrug eruptionspt_PT
dc.subjectLamotriginept_PT
dc.titleDrug Reaction With Eosinophilia and Systemic Symptoms Syndrome in a Patient Taking Lamotriginept_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceLondonpt_PT
oaire.citation.titleBMJ Case Reportspt_PT
rcaap.rightsclosedAccesspt_PT
rcaap.typearticlept_PT

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