Gabrielsen T O, Rajka G, Rustenberg B
Z Hautkr. 1985 Nov 15;60(22):1793-6.
We report on a 4-year-old boy suffering from typical infantile papular acrodermatitis with an unusual course. The eruption occurred seven weeks before the signs and symptoms of hepatitis. Only trace concentrations of hepatitis B surface antigen (HBsAg) could be detected after three weeks history of the disease. The lesions which persisted for nine weeks were itching, and there were signs of superinfection. We found only localized lymphadenopathy. The condition developed into a chronic HBsAg carrier state.
我们报告了一名4岁男孩,患有典型的婴儿丘疹性肢端皮炎,病程异常。皮疹在肝炎的体征和症状出现前7周出现。在疾病史3周后仅检测到痕量浓度的乙型肝炎表面抗原(HBsAg)。持续9周的皮损有瘙痒,并有继发感染迹象。我们仅发现局部淋巴结病。病情发展为慢性HBsAg携带状态。