Yasuda H, Kobayashi H, Hashimoto T, Itoh K, Yamane M, Nakamura J
Department of Dermatology, Sapporo Social Insurance General Hospital, 2-1, 2-Jo, 6-Chome, Atsubetsu Chuo, Atsubetsu, Sapporo 004-8618, Japan.
Br J Dermatol. 2000 Jul;143(1):144-8. doi: 10.1046/j.1365-2133.2000.03604.x.
We describe a 40-year-old Japanese man with a 3-year history of vesiculopustular lesions resembling subcorneal pustular dermatosis. Histopathology showed subcorneal pustules containing a few acantholytic cells, and direct immunofluorescence disclosed IgA deposition in the intercellular space of the upper epidermis. Circulating IgA autoantibodies of very low titre were also demonstrated by indirect immunofluorescence. A novel cDNA transfection technique clearly detected IgA autoantibodies reactive with human desmocollin-1. Combined therapy with dapsone and etretinate improved the skin lesions. We review the clinical features of 49 patients in the literature who presented with vesiculopustular lesions and intraepidermal IgA deposition.
我们描述了一名40岁的日本男性,患有类似角层下脓疱性皮肤病的水疱脓疱性损害3年。组织病理学显示角层下脓疱内含有少量棘层松解细胞,直接免疫荧光显示在上表皮细胞间间隙有IgA沉积。间接免疫荧光也证实循环中存在极低滴度的IgA自身抗体。一种新的cDNA转染技术明确检测到与人桥粒芯胶蛋白-1反应的IgA自身抗体。氨苯砜和阿维A联合治疗改善了皮肤损害。我们回顾了文献中49例表现为水疱脓疱性损害和表皮内IgA沉积患者的临床特征。