Musculoskeletal manifestations in polymyalgia rheumatica and temporal arteritis.

dc.contributor.authorNarváez García, Francisco Javiercat
dc.contributor.authorNolla Solé, Joan Miquelcat
dc.contributor.authorNarváez, José A.cat
dc.contributor.authorClavaguera, M. T.cat
dc.contributor.authorValverde García, Josécat
dc.contributor.authorRoig Escofet, D. (Daniel)cat
dc.date.accessioned2012-03-05T12:52:33Z
dc.date.available2012-03-05T12:52:33Z
dc.date.issued2001
dc.description.abstractTo evaluate the incidence and characteristics of musculoskeletal manifestations in polymyalgia rheumatica (PMR) and temporal arteritis (TA). METHODS The records of 163 cases of PMR or TA diagnosed over a 15 year period in one area of Spain were reviewed for the presence and type of musculoskeletal manifestations. RESULTS Of 163 patients, 90 had isolated PMR and 73 had TA. Eighteen of the 90 patients (20%) with isolated PMR developed distal peripheral arthritis either at diagnosis or during the course of the disease. When it occurred, synovitis was mild, monoarticular or pauci-articular, asymmetrical, transient, and not destructive. Other distal manifestations observed in these patients were carpal tunnel syndrome and distal extremity swelling with pitting oedema. In all cases these manifestations occurred in conjunction with active PMR. As expected, PMR was the most frequent musculoskeletal manifestation in patients with TA, occurring in 56% of cases. On the contrary, only 11% of patients with TA developed peripheral arthritis. An important finding was that peripheral arthritis in these patients appears to be linked only temporally to the presence of simultaneous PMR and is not observed in its absence. Distal extremity swelling or defined polyarthritis were not observed. CONCLUSION The spectrum of distal musculoskeletal manifestations of PMR in our series is similar to that reported in other populations. By contrast, distal musculoskeletal symptoms are uncommon in TA. The almost complete absence of distal musculoskeletal manifestations in patients with pure TA suggests different mechanisms of disease in PMR and TA, supporting the view of two separate conditions or one common disease in which host susceptibility influences the clinical expression.eng
dc.format.extent4 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec535346
dc.identifier.issn0003-4967
dc.identifier.pmid11602480
dc.identifier.urihttps://hdl.handle.net/2445/22474
dc.language.isoengeng
dc.publisherBMJ Group
dc.relation.isformatofReproducció digital del document publicat a: http://dx.doi.org/10.1136/ard.60.11.1060
dc.relation.ispartofAnnals of the Rheumatic Diseases, 2001, vol. 60, núm. 11, p. 1060-1063
dc.relation.urihttp://dx.doi.org/10.1136/ard.60.11.1060
dc.rights(c) BMJ Publishing Group Ltd, 2001
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (Ciències Clíniques)
dc.subject.classificationArteritis de cèl·lules gegantscat
dc.subject.classificationAparell locomotorcat
dc.subject.classificationMiàlgiacat
dc.subject.classificationInflamaciócat
dc.subject.otherGiant cell arteritiseng
dc.subject.otherMusculoskeletal systemeng
dc.subject.otherMyalgiaeng
dc.subject.otherInflammationeng
dc.titleMusculoskeletal manifestations in polymyalgia rheumatica and temporal arteritis.eng
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

Fitxers

Paquet original

Mostrant 1 - 1 de 1
Carregant...
Miniatura
Nom:
535346.pdf
Mida:
135.19 KB
Format:
Adobe Portable Document Format