Liautaud B, Pape J W, DeHovitz J A, Thomas F, LaRoche A C, Verdier R I, Deschamps M M, Johnson W D
Haitian Study Group on Kaposi's Sarcoma and Opportunistic Infection, Port-au-Prince.
Arch Dermatol. 1989 May;125(5):629-32. doi: 10.1001/archderm.125.5.629.
During July 1983 to December 1984, we observed that 62 (46%) of 134 Haitian patients with acquired immunodeficiency syndrome had intensely pruritic eruptions for which neither specific causative nor categoric diagnoses could be established. These lesions were a presenting manifestation of acquired immunodeficiency syndrome in 79% of the patients and appeared a mean of 8 months before the diagnosis of either Kaposi's sarcoma or opportunistic infection. Lesions included erythematous round macules, papules, or nodules that first appeared on the extensor surface of the arms, but subsequently involved the legs, trunk, and face. Histologically, the lesions were characterized by varying degrees of mixed (predominantly eosinophilic) perivascular and perifollicular inflammatory cell infiltrates of the dermis. The lesions did not respond to any therapeutic regimens used and usually persisted throughout the acquired immunodeficiency syndrome illness. Demographic and laboratory data did not distinguish these patients from those without pruritic skin lesions.
1983年7月至1984年12月期间,我们观察到134例海地获得性免疫缺陷综合征患者中有62例(46%)出现剧烈瘙痒性皮疹,既无法确定具体病因,也无法进行明确诊断。这些皮疹是79%患者获得性免疫缺陷综合征的首发表现,平均出现在诊断卡波西肉瘤或机会性感染前8个月。皮疹包括红斑性圆形斑疹、丘疹或结节,最初出现在手臂伸侧表面,但随后累及腿部、躯干和面部。组织学上,这些皮疹的特征是真皮层有不同程度的混合性(以嗜酸性粒细胞为主)血管周围和毛囊周围炎性细胞浸润。这些皮疹对所使用的任何治疗方案均无反应,通常在获得性免疫缺陷综合征病程中持续存在。人口统计学和实验室数据无法将这些患者与无瘙痒性皮肤病变的患者区分开来。