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  5. Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ
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Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/18259
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dc.contributor.authorDrosos, A. A.en
dc.contributor.authorGeorgiadis, A. N.en
dc.contributor.authorMetafratzi, Z. M.en
dc.contributor.authorVoulgari, P. V.en
dc.contributor.authorEfremidis, S. C.en
dc.contributor.authorBai, M.en
dc.date.accessioned2015-11-24T18:51:26Z-
dc.date.available2015-11-24T18:51:26Z-
dc.identifier.issn0300-9742-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/18259-
dc.rightsDefault Licence-
dc.subjectBiopsy, Needleen
dc.subjectFollow-Up Studiesen
dc.subjectHistiocytosis, Sinus/*complications/*diagnosis/drug therapyen
dc.subjectHumansen
dc.subjectImmunohistochemistryen
dc.subjectMaleen
dc.subjectMethylprednisolone/therapeutic useen
dc.subjectMiddle Ageden
dc.subjectRisk Assessmenten
dc.subjectSeverity of Illness Indexen
dc.subjectSjogren's Syndrome/*complications/*diagnosis/drug therapyen
dc.subjectTomography, X-Ray Computeden
dc.subjectTreatment Outcomeen
dc.titleSinus histocytosis with massive lymphadenopathy (Rosai-Dorfman disease) in a patient with primary Sjogren's syndromeen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/15163114-
heal.identifier.secondaryhttp://informahealthcare.com/doi/abs/10.1080/03009740310004739-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate2004-
heal.abstractSinus histocytosis with massive lymphadenopathy is a rare disease that has been described by Rosai and Dorfman. It is characterized by massive, cervical lymphadenopathy, with extranodal manifestations in about 40% of patients. It occurs as a distinct entity, never associated with other diseases, and in most cases the prognosis is good. Lymphadenopathy is also a frequent sign of patients with primary Sjogren's syndrome (SS), usually associated with disease activity or concurrent infection. However, excessive lymphadenopathy in SS patients is a sign of lymphoproliferative disorder development. In this report, we describe a patient with primary SS, and excessive lymphadenopathy and splenomegaly who developed Rosai-Dorfman disease, and we discuss the possible aetiopathophysiological mechanism linking these two entities.en
heal.journalNameScandinavian Journal of Rheumatologyen
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
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