Petit A, Perrin P, Bernard P, Blanchet-Bardon C, Janier M, Civatte J
Service de dermatologie, Hopital Saint-Louis, Paris, France.
Acta Derm Venereol. 1990;70(3):236-8.
A case of subepidermal autoimmune blistering disease in an 86-year-old woman is reported. Clinical features were those of a cicatricial pemphigoid, with prominent mucosal involvement leading to conjunctival and nasal scarring. Direct immunofluorescence findings were consistent with either cicatricial pemphigoid or linear IgA dermatosis, since both IgG and IgA linear deposits were found at the basal membrane zone. Immunoelectron microscopy of perilesional skin revealed IgA deposits within the lamina lucida and immunoblotting of the patient's serum disclosed IgA and IgG antibodies directed against epidermal antigens of 280, 165 and 120-130 kD.
报告了一名86岁女性的表皮下自身免疫性大疱病病例。临床特征为瘢痕性类天疱疮,伴有明显的黏膜受累,导致结膜和鼻瘢痕形成。直接免疫荧光检查结果与瘢痕性类天疱疮或线状IgA大疱性皮病一致,因为在基底膜带发现了IgG和IgA线状沉积。病损周围皮肤的免疫电镜检查显示透明层内有IgA沉积,患者血清免疫印迹显示存在针对280、165和120 - 130 kD表皮抗原的IgA和IgG抗体。