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dc.contributor.author Strickler, Alexis
dc.contributor.author Gallo, Silvanna
dc.contributor.author Jaramillo, Pedro
dc.contributor.author de Toro, Gonzalo
dc.date.accessioned 2024-09-26T00:39:53Z
dc.date.available 2024-09-26T00:39:53Z
dc.date.issued 2016-07-01
dc.identifier.issn 0370-4106
dc.identifier.uri https://repositorio.uss.cl/handle/uss/13031
dc.description Publisher Copyright: © 2016 Sociedad Chilena de Pediatría
dc.description.abstract Introduction Morphea or juvenile localised scleroderma (JLS) is an autoimmune, inflammatory, chronic, slowly progressive connective tissue disease of unknown cause that preferably affects skin and underlying tissues. Objective To report a case of Juvenil Localised scleroderma in an 8-year old girl, contributing to an early diagnosis and treatment. Clinical case The case is presented of an 8 year-old girl who presented with indurated hypopigmented plaques, of linear distribution in the right upper extremity of two years onset, together with papery texture hyperpigmented indurated plaques with whitish areas of thinned skin in right lower extremity, and leg and ankle swelling. The clinical features and diagnostic tests, including histology were compatible with linear and pansclerotic JLS. She started with immunosuppressive therapy, physiotherapy, and occupational therapy. Conclusions We report a case of linear and pansclerotic ELJ type, in which there was a 2 year delay in diagnosis, however the response to treatment was positive as expected. en
dc.language.iso eng
dc.relation.ispartof vol. 87 Issue: no. 4 Pages: 279-283
dc.source Revista Chilena de Pediatria
dc.title Morphea or juvenile localised scleroderma : Case report en
dc.title.alternative Morphea or juvenile localised sclerodermaCase report en
dc.title.alternative Morfea o esclerodermia localizada juvenil, caso clínico es
dc.type Artículo
dc.identifier.doi 10.1016/j.rchipe.2016.01.013
dc.publisher.department Facultad de Medicina y Ciencia


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