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局限性硬皮病“剑伤状”的组织学特征:一项16例病例的研究

Histological features of localized scleroderma 'en coup de sabre': a study of 16 cases.

作者信息

Taniguchi T, Asano Y, Tamaki Z, Akamata K, Aozasa N, Noda S, Takahashi T, Ichimura Y, Toyama T, Sugita M, Sumida H, Kuwano Y, Miyazaki M, Yanaba K, Sato S

机构信息

Department of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.

出版信息

J Eur Acad Dermatol Venereol. 2014 Dec;28(12):1805-10. doi: 10.1111/jdv.12280. Epub 2013 Oct 10.

Abstract

BACKGROUND

Early lesions of localized scleroderma are histologically characterized by perivascular lymphocytic infiltrate in the reticular dermis and swollen endothelial cells. However, there have been few information regarding histological features other than these findings in localized scleroderma.

OBJECTIVE

Since en coup de sabre (ECDS) is a certain subset of localized scleroderma with a relatively uniform clinical manifestation, we focused on this disease subset and evaluated its histopathological features.

METHODS

A total of 16 patients with ECDS were retrospectively evaluated on the basis of clinical and histological findings.

RESULTS

Regardless of clinical manifestations, vacuolar degeneration was found in all of the ECDS patients. Importantly, keratinocyte necroses were restricted to early and active ECDS lesions. In early ECDS patients (disease duration of <3 years), moderate to severe perivascular and/or periappendageal lymphocytic infiltrate and vacuolar changes in follicular epithelium were more prominent, whereas epidermal atrophy was less frequently observed, than in late ECDS patients (disease duration of ≥6 years).

CONCLUSION

Vacuolar degeneration at the dermoepidermal junction is a common histological feature in ECDS and perivascular and/or periappendageal lymphocytic infiltrate and vacuolar degeneration of follicular epithelium are characteristic especially in early ECDS, further supporting a canonical idea that the elimination of mutated epidermal cells by immune surveillance contributes to tissue damage and resultant fibrosis in localized scleroderma.

摘要

背景

局限性硬皮病的早期病变在组织学上的特征为网状真皮层血管周围淋巴细胞浸润和内皮细胞肿胀。然而,关于局限性硬皮病除这些表现之外的组织学特征的信息较少。

目的

由于剑伤样硬皮病(ECDS)是局限性硬皮病的一个特定亚组,具有相对一致的临床表现,我们聚焦于这个疾病亚组并评估其组织病理学特征。

方法

基于临床和组织学表现对16例ECDS患者进行回顾性评估。

结果

无论临床表现如何,所有ECDS患者均发现有液泡变性。重要的是,角质形成细胞坏死仅限于早期和活动期ECDS病变。与晚期ECDS患者(病程≥6年)相比,早期ECDS患者(病程<3年)血管周围和/或附件周围中度至重度淋巴细胞浸润以及毛囊上皮的液泡变化更为突出,而表皮萎缩较少见。

结论

真皮表皮交界处的液泡变性是ECDS常见的组织学特征,血管周围和/或附件周围淋巴细胞浸润以及毛囊上皮的液泡变性是ECDS尤其是早期ECDS的特征,进一步支持了一个经典观点,即免疫监视清除突变的表皮细胞导致局限性硬皮病的组织损伤和由此产生的纤维化。

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