Síndrome de Sjögren primária e miosite de corpos de inclusão

Publication

dc.contributor.author	Monteiro, P
dc.contributor.author	Coutinho, M
dc.contributor.author	Salvador, MJ
dc.contributor.author	Malcata, AB
dc.date.accessioned	2009-06-08T15:46:45Z
dc.date.available	2009-06-08T15:46:45Z
dc.date.issued	2009
dc.description.abstract	The authors report the case of a 69-years-old woman with Sjögren's syndrome. After 8 years of disease she developed muscle weakness and the diagnosis of inclusion body myositis was established. This is a rare association. The patient had a good response to the immunosupressive treatment. Similar cases can be found in the literature and there seems to be a subset of inclusion body myositis associated with autoimmune diseases that shows a better response to treatment and a more favourable prognosis.	en
dc.identifier.citation	Acta Reumatol Port. 2009 Apr-Jun;34(2):261-5.	en
dc.identifier.uri	http://hdl.handle.net/10400.4/520
dc.language.iso	por	en
dc.publisher	Sociedade Portuguesa de Reumatologia	en
dc.rights.uri	openAccess	en
dc.subject	Síndrome de Sjögren	en
dc.subject	Miosite	en
dc.title	Síndrome de Sjögren primária e miosite de corpos de inclusão	en
dc.title.alternative	Primary Sjögren syndrome and inclusion body myositis	en
dc.type	journal article
dspace.entity.type	Publication
rcaap.type	article	en