Millard P R, Young E, Harrison D E, Wojnarowska F
Histopathology. 1986 Oct;10(10):1047-56. doi: 10.1111/j.1365-2559.1986.tb02541.x.
Reactive perforating collagenosis is an uncommon disorder and few accounts refer to ultrastructural features. This report includes a study by light and transmission electron microscopy of serially sectioned biopsies from early lesions in two patients. Immunohistological investigations utilizing antibodies to basement membrane, laminin, collagen and cytokeratin were also done. Collagen and elastin were demonstrated within the centre of the lesions and there was a defect in the basal lamina at the base of the lesion. The collagen, cytokeratin and the basal lamina in the lesions were antigenically similar to those in the surrounding normal skin. These results are compared with previous findings and discussed in the light of the current views on the pathogenesis of this disorder.
反应性穿通性胶原病是一种罕见的疾病,很少有文献提及超微结构特征。本报告包括对两名患者早期病变连续切片活检进行光镜和透射电镜研究。还利用针对基底膜、层粘连蛋白、胶原蛋白和细胞角蛋白的抗体进行了免疫组织学研究。在病变中心发现了胶原蛋白和弹性蛋白,病变底部的基膜存在缺陷。病变中的胶原蛋白、细胞角蛋白和基膜在抗原性上与周围正常皮肤中的相似。将这些结果与先前的发现进行了比较,并根据目前对该疾病发病机制的观点进行了讨论。