4.6 Article

Update on morphea Part I. Epidemiology, clinical presentation, and pathogenesis

Journal

JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY
Volume 64, Issue 2, Pages 217-228

Publisher

MOSBY-ELSEVIER
DOI: 10.1016/j.jaad.2010.05.045

Keywords

autoimmune connective tissue disorder; fibrosing disorders; localized scleroderma; morphea; scleroderma; systemic sclerosis

Categories

Funding

  1. Department of Veterans Affairs Veterans Health Administration, Office of Research and Development, Biomedical Laboratory Research and Development
  2. National Institutes of Health [NIH K24-AR 02207]

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Morphea, also known as localized scleroderma, is a rare fibrosing disorder of the skin and underlying tissues. Morphea is differentiated from systemic sclerosis based on the absence of sclerodactyly, Raynaud phenomenon, and nailfold capillary changes. Patients with morphea commonly have systemic symptoms, such as malaise, fatigue, arthralgias, and myalgias, as well as positive autoantibody serologies. However, involvement of morphea is almost uniformly limited to those tissues derived from the mesoderm. The underlying pathogenesis of morphea is incompletely understood at this time, but ultimately results in an imbalance of collagen production and destruction. (J Am Acad Dermatol 2011;64:217-28.)

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