Miyagawa Fumi, Nakajima Anna, Akai Yasuhiro, Asada Hideo
Department of Dermatology, Nara Medical University School of Medicine, Kashihara, Japan.
The Center for Rheumatic Diseases, Nara Medical University School of Medicine, Kashihara, Japan.
Case Rep Dermatol. 2018 Oct 18;10(3):226-230. doi: 10.1159/000493180. eCollection 2018 Sep-Dec.
We report the case of a 45-year-old female with generalized morphea (GM), who exhibited positivity for the anti-centromere antibody (Ab). She frequently developed multiple sclerotic skin lesions, whose histological findings were compatible with morphea. She demonstrated favorable responses to topical and oral steroids. Cases of GM associated with systemic sclerosis (SSc)-specific Abs (anti-Scl-70 Ab, anti-centromere Ab, and anti-RNA polymerase III Ab) have rarely been reported. The previously reported GM cases involving anti-SSc-specific Abs exhibited some skin manifestations of SSc, such as nailfold capillary changes. However, our case did not show any signs of SSc or limited cutaneous SSc. More cases are needed to clarify whether GM with SSc-specific Abs leads to SSc.
我们报告了一例45岁患有泛发性硬斑病(GM)的女性病例,其抗着丝点抗体(Ab)呈阳性。她频繁出现多发性硬化性皮肤病变,组织学检查结果与硬斑病相符。她对局部和口服类固醇治疗反应良好。与系统性硬化症(SSc)特异性抗体(抗Scl-70抗体、抗着丝点抗体和抗RNA聚合酶III抗体)相关的GM病例鲜有报道。先前报道的涉及抗SSc特异性抗体的GM病例表现出一些SSc的皮肤表现,如甲襞毛细血管改变。然而,我们的病例未显示出任何SSc或局限性皮肤型SSc的迹象。需要更多病例来阐明伴有SSc特异性抗体的GM是否会发展为SSc。