Tomasini C, Soro E, Pippione M
Department of Medical and Surgical Specialties, Second Dermatologic Clinic, Turin, Italy.
Am J Dermatopathol. 2000 Aug;22(4):334-8. doi: 10.1097/00000372-200008000-00007.
Reactive angioendotheliomatosis (RA) is a rare self-limited skin condition characterized histopathologically by a proliferation of endothelial cells within vascular lumina, usually as a result of different stimuli such as systemic infections, cryoproteinemias, monoclonal gammopathies, allergic conditions, severe peripheral vascular atherosclerotic disease, and iatrogenic arteriovenous fistulas. We report on a 67-year-old woman with a 20-year history of seropositive rheumatoid arthritis who presented with violaceous swelling of her left forearm. A skin biopsy revealed the histopathologic finding of RA with focal glomeruloid features and deposition of periodic acid-Schiff-positive material. In this systemic disorder, cutaneous manifestations may occur secondary to an immune complex-mediated vasculitic mechanism.
反应性血管内皮瘤病(RA)是一种罕见的自限性皮肤病,其组织病理学特征为血管腔内内皮细胞增生,通常由不同刺激因素引起,如全身感染、冷球蛋白血症、单克隆丙种球蛋白病、过敏状态、严重外周血管动脉粥样硬化疾病和医源性动静脉瘘。我们报告一例67岁女性,有20年血清阳性类风湿关节炎病史,出现左前臂紫罗兰色肿胀。皮肤活检显示RA的组织病理学表现,伴有局灶性肾小球样特征和过碘酸-希夫阳性物质沉积。在这种全身性疾病中,皮肤表现可能继发于免疫复合物介导的血管炎机制。