Eosinophilic fasciitis-progression to linear scleroderma ( A case report )
| dc.contributor.author | Balat, Ayşe | |
| dc.contributor.author | Akıncı, Ayşehan | |
| dc.contributor.author | Mızrak, Bülent | |
| dc.contributor.author | Aydın, Abdullah | |
| dc.date.accessioned | 2021-10-20T13:17:29Z | |
| dc.date.available | 2021-10-20T13:17:29Z | |
| dc.date.issued | 1999 | |
| dc.department | İnönü Üniversitesi | en_US |
| dc.description.abstract | Abstract: Eosinophilic 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.citation | BALAT A,AKINCI A,TURGUT M,MIZRAK B,AYDIN A (1999). Eosinophilic fasciitis-progression to linear scleroderma ( A case report ). Turkish Journal of Pediatrics, 41(3), 381 - 385. | en_US |
| dc.identifier.endpage | 385 | en_US |
| dc.identifier.issn | 0041-4301 | |
| dc.identifier.issue | 3 | en_US |
| dc.identifier.startpage | 381 | en_US |
| dc.identifier.trdizinid | 9347 | en_US |
| dc.identifier.uri | https://hdl.handle.net/11616/42366 | |
| dc.identifier.uri | https://search.trdizin.gov.tr/yayin/detay/9347 | |
| dc.identifier.volume | 41 | en_US |
| dc.indekslendigikaynak | TR-Dizin | en_US |
| dc.language.iso | tr | en_US |
| dc.relation.ispartof | Turkish Journal of Pediatrics | en_US |
| dc.relation.publicationcategory | Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.title | Eosinophilic fasciitis-progression to linear scleroderma ( A case report ) | en_US |
| dc.type | Article | en_US |
