Eosinophilic fasciitis - Progression to linear scleroderma - A case report

Basit Öğe Kaydı
dc.authoridBalat, Ayse/0000-0002-8904-1348
dc.authorwosidBalat, Ayse/JOZ-8426-2023
dc.contributor.authorBalat, A
dc.contributor.authorAkinci, A
dc.contributor.authorTurgut, M
dc.contributor.authorMizrak, B
dc.contributor.authorAydin, A
dc.date.accessioned2024-08-04T20:58:40Z
dc.date.available2024-08-04T20:58:40Z
dc.date.issued1999
dc.departmentİnönü Üniversitesien_US
dc.description.abstractEosinophilic 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.startpage381en_US
dc.identifier.urihttps://hdl.handle.net/11616/103065
dc.identifier.volume41en_US
dc.identifier.wosWOS:000083042800015en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherTurkish J Pediatricsen_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.subjecteosinophilic fasciitisen_US
dc.subjectchildhood sclerodermaen_US
dc.titleEosinophilic fasciitis - Progression to linear scleroderma - A case reporten_US
dc.typeArticleen_US

Dosyalar

Koleksiyon

WoS İndeksli Yayınlar Koleksiyonu
PubMed İndeksli Yayın Koleksiyonu