Localized cutaneous fibrosing disorders

Rheum Dis Clin North Am. 2013 May;39(2):347-64. doi: 10.1016/j.rdc.2013.02.013. Epub 2013 Mar 16.

Abstract

This article acquaints the reader with disorders of the skin that might mimic systemic sclerosis but whose pathology is localized to the skin and/or has extracutaneous manifestations that are different than systemic sclerosis. These disorders include localized scleroderma (morphea), eosinophilic fasciitis, scleredema, scleromyxedema, nephrogenic systemic fibrosis, and chronic graft-versus-host disease. Particular emphasis is placed on clinical and histopathologic features that help the clinician differentiate between these disorders. Treatment options are briefly reviewed.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Chronic Disease
  • Diagnosis, Differential
  • Eosinophilia / diagnosis
  • Eosinophilia / physiopathology
  • Fasciitis / diagnosis
  • Fasciitis / physiopathology
  • Graft vs Host Disease / diagnosis
  • Graft vs Host Disease / physiopathology
  • Humans
  • Interdisciplinary Communication
  • Nephrogenic Fibrosing Dermopathy / diagnosis
  • Nephrogenic Fibrosing Dermopathy / physiopathology
  • Scleredema Adultorum / diagnosis
  • Scleredema Adultorum / physiopathology
  • Scleroderma, Localized / diagnosis
  • Scleroderma, Localized / physiopathology
  • Scleroderma, Systemic / diagnosis*
  • Scleroderma, Systemic / physiopathology
  • Scleromyxedema / diagnosis
  • Scleromyxedema / physiopathology
  • Skin Diseases / diagnosis*
  • Skin Diseases / physiopathology
  • Skin Diseases / therapy

Supplementary concepts

  • Eosinophilic Fasciitis