Careta Mariana Figueiroa, Romiti Ricardo
University of São Paulo, São Paulo, SP, Brazil.
An Bras Dermatol. 2015 Jan-Feb;90(1):62-73. doi: 10.1590/abd1806-4841.20152890.
Scleroderma is a rare connective tissue disease that is manifested by cutaneous sclerosis and variable systemic involvement. Two categories of scleroderma are known: systemic sclerosis, characterized by cutaneous sclerosis and visceral involvement, and localized scleroderma or morphea which classically presents benign and self-limited evolution and is confined to the skin and/or underlying tissues. Localized scleroderma is a rare disease of unknown etiology. Recent studies show that the localized form may affect internal organs and have variable morbidity. Treatment should be started very early, before complications occur due to the high morbidity of localized scleroderma. In this review, we report the most important aspects and particularities in the treatment of patients diagnosed with localized scleroderma.
硬皮病是一种罕见的结缔组织疾病,表现为皮肤硬化和不同程度的全身受累。已知硬皮病有两类:系统性硬化症,其特征为皮肤硬化和内脏受累;局限性硬皮病或硬斑病,通常表现为良性且自限性病程,局限于皮肤和/或其下方组织。局限性硬皮病是一种病因不明的罕见疾病。最近的研究表明,局限性硬皮病可能会影响内脏器官,且发病率各异。由于局限性硬皮病发病率较高,应在并发症出现之前尽早开始治疗。在本综述中,我们报告了诊断为局限性硬皮病患者治疗中的最重要方面和特殊性。