Department of Dermatology, Rambam Health Care Campus, Haifa, Israel.
The Ruth & Bruce Rappaport Faculty of Medicine, Haifa, Israel.
Am J Dermatopathol. 2022 Aug 1;44(8):590-593. doi: 10.1097/DAD.0000000000002226. Epub 2022 May 30.
Eccrine squamous syringometaplasia (ESS) has been associated with several conditions including morphea, linear scleroderma, and burns. It is yet to be reported in lichen sclerosus et atrophicus (LSA). We describe a bullous LSA plaque on the forearm of a woman with pre-existing genital LSA and vitiligo. Besides the histopathological findings of bullous LSA, numerous small irregular squamoid structures were present in the mid and upper dermis always above the normal eccrine glands. The histopathology, periodic acid-Schiff stain, and positive immunostains for P63, low molecular weight keratins 8&18, epithelial membrane antigen, and carcinoembryonic antigen supported the diagnosis of ESS. The pathogenesis of ESS in LSA may be related to ischemia, inflammation, and fibrosis.
汗管鳞状细胞化生(ESS)与多种疾病有关,包括硬斑病、线状硬皮病和烧伤。在萎缩性硬化性苔藓(LSA)中尚未报道。我们描述了一名女性前臂的水疱性 LSA 斑块,该女性患有先前存在的生殖器 LSA 和白癜风。除了水疱性 LSA 的组织病理学发现外,在中上层真皮中始终在正常的小汗腺上方存在许多不规则的小鳞片状结构。组织病理学、过碘酸希夫染色以及 P63、低分子量角蛋白 8&18、上皮膜抗原和癌胚抗原的免疫染色均支持 ESS 的诊断。LSA 中 ESS 的发病机制可能与缺血、炎症和纤维化有关。