Pérez A, Rodríguez M, Febrer I, Aliaga A
Department of Dermatology, Hospital General Universitario, Valencia, Spain.
Am J Dermatopathol. 1995 Aug;17(4):384-8. doi: 10.1097/00000372-199508000-00014.
Sinus histiocytosis with massive lymphadenopathy is an uncommon disease affecting individuals of either sex and of all ages and ethnic backgrounds. We present a case of sinus histiocytosis confined to the skin in a 65-year-old woman whose diagnosis was coincident with herpes simplex virus infection and polybacterial urinary infection, both asymptomatic. The polymerase chain reaction for herpes simplex virus and human herpesvirus-6 from involved skin was negative. We review previously published cases of sinus histiocytosis limited to the skin.
伴巨大淋巴结病的窦性组织细胞增生症是一种罕见疾病,可发生于任何年龄、性别及种族背景的个体。我们报告一例65岁女性的窦性组织细胞增生症,病变局限于皮肤,其诊断与单纯疱疹病毒感染及多种细菌引起的无症状尿路感染同时发生。对受累皮肤进行单纯疱疹病毒和人疱疹病毒6型的聚合酶链反应检测均为阴性。我们回顾了既往发表的病变局限于皮肤的窦性组织细胞增生症病例。