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

被引:251
作者
Fett, Nicole [1 ]
Werth, Victoria P.
机构
[1] Univ Penn, Sch Med, Dept Dermatol, Perelman Ctr Adv Med, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
autoimmune connective tissue disorder; fibrosing disorders; localized scleroderma; morphea; scleroderma; systemic sclerosis; SCLEROSUS-ET-ATROPHICUS; OF-THE-LITERATURE; BORRELIA-BURGDORFERI INFECTION; JUVENILE LOCALIZED SCLERODERMA; DISABLING PANSCLEROTIC MORPHEA; PROGRESSIVE FACIAL HEMIATROPHY; POLYMERASE-CHAIN-REACTION; SYSTEMIC-SCLEROSIS; RAYNAUDS-PHENOMENON; EN-COUP;
D O I
10.1016/j.jaad.2010.05.045
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100227 [皮肤病学];
摘要
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.)
引用
收藏
页码:217 / 228
页数:12
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