Doença pulmonar intersticial como manifestação isolada de sindrome anti-sintetase

Publication

dc.contributor.author	Monteiro, P
dc.contributor.author	Coutinho, M
dc.contributor.author	Machado, P
dc.contributor.author	Garcia, J
dc.contributor.author	Salvador, MJ
dc.contributor.author	Inês, L
dc.contributor.author	Silva, J
dc.contributor.author	Malcata, AB
dc.date.accessioned	2009-06-08T15:46:34Z
dc.date.available	2009-06-08T15:46:34Z
dc.date.issued	2009
dc.description.abstract	The 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.citation	Acta Reumatol Port. 2009 Apr-Jun;34(2):256-60	en
dc.identifier.uri	http://hdl.handle.net/10400.4/519
dc.language.iso	por	en
dc.publisher	Sociedade Portuguesa de Reumatologia	en
dc.rights.uri	openAccess	en
dc.subject	Doença Pulmonar Intersticial	en
dc.title	Doença pulmonar intersticial como manifestação isolada de sindrome anti-sintetase	en
dc.title.alternative	Intersticial lung disease as the sole manifestation of antisynthetase syndrome	en
dc.type	journal article
dspace.entity.type	Publication
rcaap.type	article	en