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系统性硬皮病并发由柯本现象引起的局限性硬皮病样病变。

Systemic sclerosis complicated with localized scleroderma-like lesions induced by Köbner phenomenon.

机构信息

Department of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo 113-8655, Japan.

Department of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo 113-8655, Japan.

出版信息

J Dermatol Sci. 2018 Mar;89(3):282-289. doi: 10.1016/j.jdermsci.2017.12.005. Epub 2017 Dec 16.

DOI:10.1016/j.jdermsci.2017.12.005
PMID:29279288
Abstract

BACKGROUND

Scleroderma is a chronic disease of unknown etiology characterized by skin fibrosis and is divided into two clinical entities: systemic sclerosis (SSc) and localized scleroderma (LSc). In general, LSc is rarely complicated with SSc, but a certain portion of SSc patients manifests bilateral symmetric LSc-like lesions on the trunk and extremities.

OBJECTIVE

We investigated SSc patients with LSc-like lesions to clarify the underlying pathophysiology.

METHODS

Nine SSc cases complicated with LSc-like lesions were clinically and histologically characterized.

RESULTS

SSc patients with LSc-like lesions exhibited multiple progressive hyper- and/or hypo-pigmented plaques with mild sclerosis symmetrically distributed on the trunk and extremities, especially abdominal region. In histological assessment, epidermal IL-1α expression was elevated in both forearms and LSc-like lesions of these patients to a greater extent than in forearms of control patients (SSc patients without LSc-like lesions). Of note, the infiltration and degranulation of mast cells were evident throughout the dermis of LSc-like lesions, while detectable to a lesser extent in forearms of SSc patients with LSc-like lesions and control patients.

CONCLUSION

The epidermis of SSc patients with LSc-like lesions seems to possess an inflammatory phenotype, leading to the activation of mast cells in the dermis of mechanically stressed skin. Köbner phenomenon may be involved in the induction of LSc-like lesions in a certain subset of SSc.

摘要

背景

硬皮病是一种病因不明的慢性疾病,其特征为皮肤纤维化,并分为两种临床实体:系统性硬皮病(SSc)和局限性硬皮病(LSc)。一般来说,LSc 很少与 SSc 同时发生,但部分 SSc 患者的躯干和四肢会出现双侧对称的 LSc 样病变。

目的

我们研究了具有 LSc 样病变的 SSc 患者,以阐明其潜在的病理生理学机制。

方法

我们对 9 例具有 LSc 样病变的 SSc 病例进行了临床和组织学特征分析。

结果

具有 LSc 样病变的 SSc 患者表现为多发性进行性色素沉着过度和/或色素减退斑,伴有轻度硬化,对称分布于躯干和四肢,尤其是腹部。在组织学评估中,前臂和这些患者的 LSc 样病变中表皮 IL-1α 的表达明显高于对照组患者(无 LSc 样病变的 SSc 患者)。值得注意的是,肥大细胞的浸润和脱颗粒在 LSc 样病变的整个真皮中都很明显,而在具有 LSc 样病变的 SSc 患者的前臂和对照组患者中则不太明显。

结论

具有 LSc 样病变的 SSc 患者的表皮似乎具有炎症表型,导致真皮中的肥大细胞被激活。机械性应激皮肤中的 Koebner 现象可能参与了某些 SSc 患者中 LSc 样病变的诱导。

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