皮肌炎的皮肤溃疡:抗nxp -2/抗tif1 - γ抗体阳性的病例报告。

Dermatologie (Heidelberg, Germany) Pub Date : 2025-02-01 Epub Date: 2025-01-16 DOI:10.1007/s00105-024-05462-0
Caroline Wald, Jan-Christoph Simon, Regina Treudler
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引用次数: 0

摘要

一名33岁女性面部和躯干部位出现抗恩智普2阳性皮肌炎,一名67岁女性手部出现tif1 - γ阳性皮肌炎,她们分别接受了硫唑嘌呤或低剂量甲基强的松龙的全身治疗,并循环静脉注射免疫球蛋白(IVIG)。在实验室检查中,两例患者的抗mda‑5抗体状态均为阴性,肌酸激酶(CK)正常,而组织病理学检查无特异性。局部强化4级皮质类固醇治疗和持续免疫抑制或免疫调节治疗导致溃疡性皮肤病变愈合。本报告旨在提高人们对抗恩智浦-2或抗tif1 - γ阳性皮肌炎中皮肤溃疡罕见发生的认识,因为溃疡可能与严重的疾病病程有关。在我们的两个病人的情况下,它完全是一个皮肤的表现,没有其他并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Cutaneous ulceration in dermatomyositis : Case reports with positive anti-NXP-2/anti-TIF1-gamma antibody status].

Painful ulcerations developed in a 33-year-old woman with anti-NXP-2-positive dermatomyositis in the facial and trunk areas and a 67-year-old woman with TIF1-gamma-positive dermatomyositis on the hands, while undergoing systemic therapy with azathioprine or low-dose methylprednisolone and cyclic administration of intravenous immunoglobulins (IVIG), respectively. In the laboratory workup, the anti-MDA‑5 antibody status remained negative and the creatine kinase (CK) normal in both patients, while histopathological examinations were nonspecific. Intensive topical class 4 corticosteroid therapy and continuation of the immunosuppressive or immunomodulating therapy led to healing of the ulcerative skin lesions. This report aims to raise awareness of the rare occurrence of cutaneous ulceration in anti-NXP-2- or anti-TIF1-gamma-positive dermatomyositis, as ulcerations may be associated with a severe disease course. In both of our patient cases, it is exclusively a dermal manifestation without other complications.

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