Gharami Ramesh C, Kumar Piyush, Mondal Avijit, Ghosh Kalyan
Dermatology, Medical College, Kolkata, India.
Dermatol Online J. 2010 Jul 15;16(7):10.
Dyshidrosiform Bullous pemphigoid is a well-known entity, but dyshidrosiform pemphigus vulgaris has rarely been described. Our patient, a 36-year-old female, with a known case of pemphigus vulgaris (PV) for the last 6 years, presented with a 3 month history of a dyshidrosiform eruption of the soles. On the basis of histopathological and direct immunofluorence (DIF) findings, the new eruption was diagnosed as PV. We report our case as dyshidrosiform pemphigus vulgaris.
汗疱疹样大疱性类天疱疮是一种众所周知的疾病,但汗疱疹样寻常型天疱疮却鲜有报道。我们的患者是一名36岁女性,在过去6年中确诊为寻常型天疱疮(PV),此次因足底出现汗疱疹样皮疹3个月前来就诊。根据组织病理学和直接免疫荧光(DIF)检查结果,新出现的皮疹被诊断为PV。我们将该病例报告为汗疱疹样寻常型天疱疮。