Mizutani H, Taniguchi H, Sakakura T, Shimizu M
Department of Dermatology, Mie University Faculty of Medicine, Tsu, Japan.
J Dermatol. 1995 Apr;22(4):267-71. doi: 10.1111/j.1346-8138.1995.tb03384.x.
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.
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。