Destro M, Wallow I H, Brightbill F S
Arch Ophthalmol. 1987 Sep;105(9):1248-52. doi: 10.1001/archopht.1987.01060090106038.
Recessive epidermolysis bullosa dystrophica (REBD), a bullous disorder of the skin and mucous membranes, is frequently associated with ocular complications. A 40-year-old woman presented with lid ulcerations, chronic conjunctivitis, diffuse subepithelial corneal scarring, corneal ulceration, and cataracts. Management with intensive lubricant therapy, soft-bandage contact lenses, and cataract extraction successfully restored her sight. Histologic examination via light and electron microscopy revealed blister formation and scarring beneath the epithelial basement membrane of both the skin and cornea, confirming the diagnosis of REBD. The ultrastructure of the skin and cornea and the ocular complications of the major forms of epidermolysis are described herein. To our knowledge, successful ocular management of a confirmed case of REBD with complete ocular histopathologic features has not been documented.
隐性营养不良性大疱性表皮松解症(REBD)是一种皮肤和黏膜的大疱性疾病,常伴有眼部并发症。一名40岁女性出现眼睑溃疡、慢性结膜炎、弥漫性上皮下角膜瘢痕形成、角膜溃疡和白内障。通过强化润滑剂治疗、软性绷带角膜接触镜和白内障摘除术成功恢复了她的视力。光镜和电镜组织学检查显示皮肤和角膜上皮基底膜下有水泡形成和瘢痕,证实了REBD的诊断。本文描述了皮肤和角膜的超微结构以及主要类型表皮松解症的眼部并发症。据我们所知,尚未有关于具有完整眼部组织病理学特征的确诊REBD病例成功眼部治疗的文献记载。