Rybojad M, Leblanc T, Flageul B, Bernard P, Morel P, Schaison G, D'Agay M F, Borradori L
Service de Dermatologie, Hôpital Saint Louis, Paris, France.
Br J Dermatol. 1993 Apr;128(4):418-22. doi: 10.1111/j.1365-2133.1993.tb00202.x.
We report a child with a T-cell lymphoblastic lymphoma, and a widespread erosive mucocutaneous eruption, whose clinical and immunopathological features were consistent with a diagnosis of paraneoplastic pemphigus. Direct immunofluorescence showed deposition of C3 in the epidermal intercellular spaces, and in a linear pattern along the dermo-epidermal junction. Circulating autoantibodies binding in a pemphigus-like pattern to mouse urinary bladder epithelium were found. By Western immunoblotting, the patient's serum recognized two epidermal polypeptides with molecular weights of 210 and 190 kDa. No reactivity with the 230-kDa bullous pemphigoid antigen and the 250-kDa desmoplakin I antigen was found.
我们报告了一名患有T细胞淋巴母细胞淋巴瘤且伴有广泛糜烂性黏膜皮肤疹的儿童,其临床和免疫病理特征符合副肿瘤性天疱疮的诊断。直接免疫荧光显示C3沉积于表皮细胞间间隙,并沿真皮-表皮交界处呈线性分布。发现循环自身抗体以天疱疮样模式与小鼠膀胱上皮结合。通过蛋白质免疫印迹法,患者血清识别出两条分子量分别为210 kDa和190 kDa的表皮多肽。未发现与230 kDa的大疱性类天疱疮抗原和250 kDa的桥粒斑蛋白I抗原发生反应。