Medenica-Mojsilović L, Fenske N A, Espinoza C G
Am J Dermatopathol. 1987 Aug;9(4):324-33.
A case of epidermolysis bullosa acquisita (EBA), associated with inflammatory bowel disease in which cicatricial alopecia was present, was studied by electron microscopy and direct immunofluorescence microscopy. Direct immunofluorescence studies were performed on both clinically normal and perilesional skin, with and without previous separation of the epidermis from the dermis by incubation with 1 M sodium chloride. We propose the use of this separation technique to identify the level of antibody deposition in patients with EBA in whom circulating antibodies are lacking. This technique may be particularly beneficial in delineating between EBA and the clinically similar scarring localized forms of bullous pemphigoid in which circulating antibodies are often absent.
对1例获得性大疱性表皮松解症(EBA)进行了研究,该病例与炎性肠病相关且存在瘢痕性脱发,采用电子显微镜和直接免疫荧光显微镜检查。对临床正常皮肤和皮损周围皮肤进行直接免疫荧光研究,在有或没有预先通过与1 M氯化钠孵育使表皮与真皮分离的情况下进行。我们建议使用这种分离技术来确定缺乏循环抗体的EBA患者中抗体沉积的水平。该技术在区分EBA和临床相似的瘢痕性局限性大疱性类天疱疮(后者通常缺乏循环抗体)方面可能特别有用。