Schenk P, Konrad K
Laryngol Rhinol Otol (Stuttg). 1983 Oct;62(10):456-62.
Epidermolysis bullosa acquisita is a rare acquired mechanobullous disorder which in contrast to the other types of epidermolysis bullosa is not hereditary. Skin lesions and, for the first time, lesions of the mucous membranes of the upper respiratory tract and oesophagus were studied by light and electron microscopic and immunofluorescence and immunoelectron microscopic methods. Immunofluorescence studies demonstrated linear IgG and complement deposits along the basement membrane zone. Electron microscopy of skin and mucosa revealed a dermolytic subbasal-lamina type of blister formation, diminished and rudimentary anchoring fibrils, and a zone of amorphous material beneath the basal lamina (lamina densa). Immunoelectron microscopic studies demonstrated the deposition of immunoglobulins in the amorphous zone beneath the basal lamina along the dermal-epidermal junction. The results are discussed in terms of current immunological findings.
获得性大疱性表皮松解症是一种罕见的获得性机械性大疱性疾病,与其他类型的大疱性表皮松解症不同,它不是遗传性的。采用光镜、电镜、免疫荧光和免疫电镜方法对皮肤病变以及首次对上呼吸道和食管黏膜病变进行了研究。免疫荧光研究显示沿基底膜带呈线性IgG和补体沉积。皮肤和黏膜的电子显微镜检查显示为真皮松解性基底膜下型水疱形成、锚定原纤维减少和发育不全,以及基底膜(致密板)下方的无定形物质带。免疫电镜研究显示免疫球蛋白沿真皮-表皮交界处沉积在基底膜下方的无定形区域。根据当前的免疫学研究结果对这些结果进行了讨论。