Lacour J P, Perrin C, Ortonne J P
Service de Dermatologie, Université de Nice, France.
Dermatology. 1993;186(3):190-2. doi: 10.1159/000247343.
We report a new case of Ofuji papuloerythroderma. There was no obvious sign of lymphoma or underlying malignancy. This is the 7th European case of papuloerythroderma. This recently described clinical entity is characterized by a pruritic eruption of widespread red-brown flat papules sparing the skin folds, with eosinophilia. The recognition, report and follow-up of further cases are necessary to clarify its relationship with paraneoplastic syndromes, hypereosinophilic syndrome, or prelymphoma skin eruptions.
我们报告一例新的Ofuji丘疹性红皮病病例。患者无明显的淋巴瘤或潜在恶性肿瘤迹象。这是欧洲第7例丘疹性红皮病病例。这种最近被描述的临床实体的特征是广泛分布的红棕色扁平丘疹伴瘙痒性皮疹，不累及皮肤褶皱处，伴有嗜酸性粒细胞增多。有必要识别、报告并随访更多病例，以阐明其与副肿瘤综合征、高嗜酸性粒细胞综合征或淋巴瘤前期皮肤皮疹的关系。
