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Doença pulmonar intersticial como manifestação isolada de sindrome anti-sintetase

dc.contributor.authorMonteiro, P
dc.contributor.authorCoutinho, M
dc.contributor.authorMachado, P
dc.contributor.authorGarcia, J
dc.contributor.authorSalvador, MJ
dc.contributor.authorInês, L
dc.contributor.authorSilva, J
dc.contributor.authorMalcata, AB
dc.date.accessioned2009-06-08T15:46:34Z
dc.date.available2009-06-08T15:46:34Z
dc.date.issued2009
dc.description.abstractThe authors report a clinical case of a woman who had a 3 years diagnosis of hipersensitivity pneumonitis based on intersticial lung disease whithout other manifestations. The diagnosis of antisynthetase syndrome was made three years after the initial symptoms upon the onset of systemic manifestations with articular involvement, myositis and determination of anti-PL 7 antibodies. In this syndrome, the isolated pulmonary involvement is rare.en
dc.identifier.citationActa Reumatol Port. 2009 Apr-Jun;34(2):256-60en
dc.identifier.urihttp://hdl.handle.net/10400.4/519
dc.language.isoporen
dc.publisherSociedade Portuguesa de Reumatologiaen
dc.rights.uriopenAccessen
dc.subjectDoença Pulmonar Intersticialen
dc.titleDoença pulmonar intersticial como manifestação isolada de sindrome anti-sintetaseen
dc.title.alternativeIntersticial lung disease as the sole manifestation of antisynthetase syndromeen
dc.typejournal article
dspace.entity.typePublication
rcaap.typearticleen

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