Esophageal manometric findings in autoimmune rheumatic diseases: is scleroderma esophagus a specific entity?

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dc.contributor.authorTsianos, E. B.en
dc.contributor.authorDrosos, A. A.en
dc.contributor.authorChiras, C. D.en
dc.contributor.authorMoutsopoulos, H. M.en
dc.contributor.authorKitridou, R. C.en
dc.date.accessioned2015-11-24T19:18:24Z
dc.date.available2015-11-24T19:18:24Z
dc.identifier.issn0172-8172-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/21862
dc.rightsDefault Licence-
dc.subjectAdolescenten
dc.subjectAdulten
dc.subjectAgeden
dc.subjectAged, 80 and overen
dc.subjectArthritis, Rheumatoid/physiopathologyen
dc.subjectAutoimmune Diseases/*physiopathologyen
dc.subjectChilden
dc.subjectConnective Tissue Diseases/physiopathologyen
dc.subjectEsophageal Diseases/*etiology/physiopathologyen
dc.subjectEsophagus/*physiopathologyen
dc.subjectFemaleen
dc.subjectHumansen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectMixed Connective Tissue Disease/physiopathologyen
dc.subjectPeristalsisen
dc.subjectPressureen
dc.subjectRaynaud Disease/physiopathologyen
dc.subjectRheumatic Diseases/complications/immunology/*physiopathologyen
dc.subjectScleroderma, Systemic/complications/*physiopathologyen
dc.subjectSjogren's Syndrome/physiopathologyen
dc.titleEsophageal manometric findings in autoimmune rheumatic diseases: is scleroderma esophagus a specific entity?en
heal.abstractIn order to assess whether distal esophageal hypomotility in scleroderma is unique to this disease or not, we studied 25 normal volunteers and 109 patients with autoimmune rheumatic diseases (27 with primary Sjogren's syndrome, 25 with idiopathic Raynaud's phenomenon, 25 with rheumatoid arthritis, 19 with scleroderma, 5 with undifferentiated connective tissue disease, 3 with systemic lupus erythematosus, 2 with mixed connective tissue disease, 2 with sclerodermatomyositis, and one with morphea). Esophageal dysfunction typical of scleroderma was present in 17 patients (15.6%), of whom 13 had scleroderma (68%) and one each primary Sjogren's syndrome, rheumatoid arthritis, undifferentiated connective tissue disease, and mixed connective tissue disease. Twenty-two percent of all patients had nonspecific esophageal motility changes, clustered among primary Sjogren's syndrome, idiopathic Raynaud's phenomenon, and rheumatoid arthritis. We conclude that lower esophageal hypomotility, although most frequent in scleroderma, is not unique to this disease and can be encountered in several other auto-immune rheumatic diseases.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/3495853-
heal.identifier.secondaryhttp://www.springerlink.com/content/m756x1hl5306n87g/fulltext.pdf-
heal.journalNameRheumatol Inten
heal.journalTypepeer-reviewed-
heal.languageen-
heal.publicationDate1987-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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