Suppr超能文献

结节性硬皮病:腱生蛋白表达局部增加,与周围硬皮病皮肤不同。

Nodular scleroderma: focally increased tenascin expression differing from that in the surrounding scleroderma skin.

作者信息

Mizutani H, Taniguchi H, Sakakura T, Shimizu M

机构信息

Department of Dermatology, Mie University Faculty of Medicine, Tsu, Japan.

出版信息

J Dermatol. 1995 Apr;22(4):267-71. doi: 10.1111/j.1346-8138.1995.tb03384.x.

Abstract

Nodular scleroderma is a rare variant of the disease, whose pathogenesis is uncertain. Tenascin is a recently cloned extracellular matrix protein which is thought to be a marker for tissue remodelling. To further investigate the pathogenesis of nodular scleroderma, we have followed up a case of this disease and studied tenascin expression in the nodular lesions and surrounding progressive systemic sclerosis skin. Previously, we demonstrated a long-lasting intermediate level of dermal tenascin expression in progressive systemic sclerosis; morphea and hypertrophic scar lesions showed strong but short-lived tenascin expression. In our current patient, high levels of tenascin were found in the nodules, which rapidly resolved. Thus, the time course of the clinical and histopathological findings together with the tenascin expression were more suggestive of hypertrophic scar than progressive systemic sclerosis. These findings imply that nodular scleroderma has a supplementary pathogenesis, such as itching, in addition to the proceeding systemic sclerosis.

摘要

结节性硬皮病是该疾病的一种罕见变体,其发病机制尚不确定。腱生蛋白是一种最近克隆出的细胞外基质蛋白,被认为是组织重塑的标志物。为了进一步研究结节性硬皮病的发病机制,我们对一例该疾病患者进行了随访,并研究了腱生蛋白在结节性病变及周围进行性系统性硬化症皮肤中的表达。此前,我们证明在进行性系统性硬化症中真皮腱生蛋白表达呈长期中等水平;硬斑病和肥厚性瘢痕病变显示腱生蛋白表达强烈但持续时间短。在我们目前的患者中,结节中发现了高水平的腱生蛋白,且这些结节迅速消退。因此,临床和组织病理学发现的时间进程以及腱生蛋白表达更提示为肥厚性瘢痕而非进行性系统性硬化症。这些发现意味着结节性硬皮病除了进行性系统性硬化症外,还有诸如瘙痒等补充性发病机制。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验