Lowe L, Hebert A A, Duvic M
Department of Dermatology, University of Texas Medical School, Houston.
J Am Acad Dermatol. 1989 Feb;20(2 Pt 2):336-8. doi: 10.1016/s0190-9622(89)70041-4.
Gianotti-Crosti syndrome, a distinctive eruption occurring after hepatitis B infection, is characterized by symmetric, nonpruritic lichenoid papules usually localized to the face, limbs, and buttocks. In North America, hepatitis B antigenemia is rarely associated with Gianotti-Crosti syndrome in infants. Recent reports indicate there are a variety of infectious agents associated with Gianotti-Crosti syndrome. We report a case of an 11-month-old white female infant with Gianotti-Crosti syndrome and concurrent primary Epstein-Barr virus infection without evidence of hepatitis B infection.
詹诺蒂-克罗西综合征是乙型肝炎感染后出现的一种独特皮疹，其特征为对称、非瘙痒性苔藓样丘疹，通常局限于面部、四肢和臀部。在北美，婴儿的乙型肝炎抗原血症很少与詹诺蒂-克罗西综合征相关。最近的报告表明，有多种感染因子与詹诺蒂-克罗西综合征有关。我们报告一例11个月大的白人女婴，患有詹诺蒂-克罗西综合征并同时感染原发性爱泼斯坦-巴尔病毒，无乙型肝炎感染证据。
