Eosinophilic fasciitis - Progression to linear scleroderma. A Case Report

Basit Öğe Kaydı
dc.authorscopusid55898957300
dc.authorscopusid7003868986
dc.authorscopusid57206323829
dc.authorscopusid56108998400
dc.authorscopusid56104637200
dc.contributor.authorBalat A.
dc.contributor.authorAkinci A.
dc.contributor.authorTurgut M.
dc.contributor.authorMizrak B.
dc.contributor.authorAydin A.
dc.date.accessioned2024-08-04T19:59:13Z
dc.date.available2024-08-04T19:59:13Z
dc.date.issued1999
dc.departmentİnönü Üniversitesien_US
dc.description.abstractEoslnophilic fasciitis is a rare disease in children. Although changes similar to linear scleroderma have been reported, the outcome is usually good. In this report, a 10-year-old boy who developed eosinophilic fasciitis without a good response to steroids is presented. He progressed to linear scleroderma within months. Our case reinforces the hypothesis that eosinophilic fasciitis may be an early manifestation or a variant of localized scleroderma similar to the other cases in the literature.en_US
dc.identifier.endpage385en_US
dc.identifier.issn0041-4301
dc.identifier.issue3en_US
dc.identifier.pmid10770102en_US
dc.identifier.scopus2-s2.0-0033156115en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage381en_US
dc.identifier.urihttps://hdl.handle.net/11616/90475
dc.identifier.volume41en_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.relation.ispartofTurkish Journal of Pediatricsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectChildhood sclerodermaen_US
dc.subjectEosinophilic fasciitisen_US
dc.titleEosinophilic fasciitis - Progression to linear scleroderma. A Case Reporten_US
dc.typeArticleen_US

Dosyalar

Koleksiyon

Scopus İndeksli Yayınlar Koleksiyonu
PubMed İndeksli Yayın Koleksiyonu