Morphea or juvenile localised scleroderma: Case report

Translated title of the contribution: Morphea or juvenile localised scleroderma: Case report

Alexis Strickler*, Silvanna Gallo, Pedro Jaramillo, Gonzalo de Toro

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

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.

Translated title of the contributionMorphea or juvenile localised scleroderma: Case report
Original languageEnglish
Pages (from-to)279-283
Number of pages5
JournalRevista Chilena de Pediatria
Volume87
Issue number4
DOIs
StatePublished - 2016

Bibliographical note

Publisher Copyright:
© 2016 Sociedad Chilena de Pediatría

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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