Jacyk W K, Simson I W, Slater D N, Leiferman K M
Department of Dermatology, University of Pretoria, Republic of South Africa.
Br J Dermatol. 1996 Mar;134(3):469-74.
We report three South African black teenage girls with extensive pruritic papular lesions arising on a pachydermatous base, resembling severe atopic dermatitis or onchodermatitis. All three had peculiar hypertrophic genital lesions and peripheral blood eosinophilia. Histological studies showed an eosinophil-rich lymphohistiocytic infiltrate and variable fibrosis. Extensive fibrillar extracellular deposition of eosinophil granule major basic protein was demonstrated by an indirect immunofluorescence technique. A beneficial therapeutic effect was obtained using dapsone, prednisolone and cetirizine. The term pachydermatous eosinophilic dermatitis is proposed and its position among other conditions characterized by peripheral blood and skin tissue eosinophilia, is discussed.
我们报告了三名南非黑人少女,她们在厚皮性基底上出现广泛的瘙痒性丘疹病变,类似严重特应性皮炎或结节性痒疹。三人都有特殊的肥厚性生殖器病变及外周血嗜酸性粒细胞增多。组织学研究显示富含嗜酸性粒细胞的淋巴组织细胞浸润和不同程度的纤维化。间接免疫荧光技术证实了嗜酸性粒细胞颗粒主要碱性蛋白在细胞外广泛的纤维状沉积。使用氨苯砜、泼尼松龙和西替利嗪获得了有益的治疗效果。我们提出了“厚皮性嗜酸性粒细胞性皮炎”这一术语,并讨论了它在其他以外周血和皮肤组织嗜酸性粒细胞增多为特征的疾病中的地位。