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.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.uri	http://hdl.handle.net/11616/42366
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.language.iso	tur	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
dc.relation.journal	Turkish Journal of Pediatrics	en_US
dc.contributor.department	İnönü Üniversitesi	en_US