Aste N, Fumo G, Conti B, Biggio P
Clinica Dermatologica, University of Cagliari, Italy.
J Eur Acad Dermatol Venereol. 2000 Jan;14(1):55-7. doi: 10.1046/j.1468-3083.2000.00003.x.
Ofuji papuloerythrodema is a rare type of dermatosis marked by an erythrodermic manifestation which is intensely pruritic and results from the coalescing of brownish papules which in the main do not involve the great folds. The authors present the case history of a 72-year-old female, whose dermatosis appeared 8 years after the diagnosis of malignant lymphocytic lymphoma. The Authors describe the clinical and histopathological picture, illustrating the laboratory results and stressing the importance of the association of the two pathologies in a possible nosological overview.
尾藤氏丘疹性红皮病是一种罕见的皮肤病，其特征为红皮病表现，伴有剧烈瘙痒，由褐色丘疹融合而成，主要不累及大的褶皱部位。作者报告了一名72岁女性的病例，其皮肤病在被诊断为恶性淋巴细胞淋巴瘤8年后出现。作者描述了临床和组织病理学表现，展示了实验室检查结果，并强调了在可能的疾病分类概述中这两种病症关联的重要性。
