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Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/21880
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dc.contributor.authorChaniotakis, I.en
dc.contributor.authorNomikos, K.en
dc.contributor.authorGamvroulia, C.en
dc.contributor.authorZioga, A.en
dc.contributor.authorStergiopoulou, C.en
dc.contributor.authorBassukas, I. D.en
dc.date.accessioned2015-11-24T19:18:35Z-
dc.date.available2015-11-24T19:18:35Z-
dc.identifier.issn1421-9832-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/21880-
dc.rightsDefault Licence-
dc.subjectAngiomatosis/drug therapy/immunology/*pathologyen
dc.subjectBiopsy, Needleen
dc.subjectChild, Preschoolen
dc.subjectDrug Therapy, Combinationen
dc.subjectFemaleen
dc.subjectFollow-Up Studiesen
dc.subjectHumansen
dc.subject*Immunocompromised Hosten
dc.subjectImmunohistochemistryen
dc.subjectMethylprednisolone/therapeutic useen
dc.subjectMiddle Ageden
dc.subjectMycophenolic Acid/analogs & derivativesen
dc.subjectPemphigus/diagnosis/drug therapy/*immunologyen
dc.subjectRisk Assessmenten
dc.subjectSeverity of Illness Indexen
dc.subjectSkin Diseases, Vascular/drug therapy/immunology/*pathologyen
dc.subjectTreatment Outcomeen
dc.titleEruptive pseudoangiomatosis: report of an adult case and unifying hypothesis of the pathogenesis of paediatric and adult casesen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primary10.1159/000102035-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/17587841-
heal.identifier.secondaryhttp://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowPDF&ArtikelNr=000102035&Ausgabe=233088&ProduktNr=224164&filename=000102035.pdf-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate2007-
heal.abstractOne month after the onset of immunosuppressive treatment with corticosteroids and mycophenolate mofetil for a newly diagnosed pemphigus vulgaris, a 50-year-old female patient developed a new eruption clinically and histomorphologically consistent with eruptive pseudoangiomatosis (EP). Its self-limited course further confirmed this diagnosis. Although initially described as a paediatric eruption, meanwhile more adult cases of EP (30 out of a total of 53 cases identified by a Medline search) are reported in the literature. The review of adult cases of EP disclosed some common clinical and epidemiological characteristics: adult EP cases tend to cluster in the Mediterranean region of Europe, develop during the summer months, sometimes in the form of limited micro-epidemics, affect immunocompromised individuals and have lesions confined to the exposed skin sites. These characteristics, together with the exanthematic nature of the disease in children, point to some vector-transmitted infectious agent as the cause of this probably underdiagnosed disease.en
heal.journalNameDermatologyen
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
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