Lee M S, Kossard S, Ho K K, Barnetson R S, Ravich R B
Skin & Cancer Foundation, Darlinghurst, New South Wales, Australia.
Australas J Dermatol. 1995 Nov;36(4):206-10. doi: 10.1111/j.1440-0960.1995.tb00976.x.
Paraneoplastic pemphigus is a recently described autoimmune disease characterized by painful mucosal ulceration and polymorphous skin lesions in association with an underlying neoplasm. Distinct autoantibodies bind desmoplakin I, desmoplakin II, bullous pemphigoid antigen and an uncharacterized 190 kDa antigen. A case is presented of paraneoplastic pemphigus that developed after radiotherapy for non-Hodgkin's lymphoma in a 53 year old man. Multiple skin biopsies showed a lichenoid reaction without acantholysis. Immunofluorescence and mucosal biopsies were required to establish the correct diagnosis. Corneal opacities resembling lichenoid graft-versus-host disease and retinal haemorrhages, which developed in the patient, have not been previously documented. Despite high doses of immunosuppressive agents and plasmaphoresis, the patient eventually died from respiratory failure.
副肿瘤性天疱疮是一种最近被描述的自身免疫性疾病,其特征为疼痛性黏膜溃疡和多形性皮肤损害,并伴有潜在的肿瘤。不同的自身抗体可结合桥粒斑蛋白I、桥粒斑蛋白II、大疱性类天疱疮抗原和一种未明确的190 kDa抗原。本文报告了一名53岁男性在接受非霍奇金淋巴瘤放疗后发生副肿瘤性天疱疮的病例。多次皮肤活检显示为苔藓样反应,无棘层松解。需要进行免疫荧光检查和黏膜活检以确立正确诊断。该患者出现的类似苔藓样移植物抗宿主病的角膜混浊和视网膜出血此前未见文献记载。尽管使用了大剂量免疫抑制剂和血浆置换术,患者最终仍死于呼吸衰竭。