Mokhtari Fatemeh, Poostiyan Nazila
Department of Dermatology, Skin Diseases and Leishmaniasis Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Adv Biomed Res. 2018 May 23;7:83. doi: 10.4103/abr.abr_21_17. eCollection 2018.
Subcorneal pustular dermatosis (SPD) or Sneddon-Wilkinson disease is a rare, benign, chronic, sterile pustular eruption which is associated with various systemic diseases including immunoglobinopathies, neoplasms, and autoimmune disorders. This paper reports a case of SPD in a patient with diffuse scleroderma in a 37-year-old woman. The hypothesis that immune dysregulation may play a role in the pathogenesis of SPD was supposed by the coexistence of diffuse scleroderma and SPD in our patient.
角层下脓疱性皮肤病(SPD)或斯内登-威尔金森病是一种罕见的、良性的、慢性的无菌性脓疱性皮疹,与包括免疫球蛋白病、肿瘤和自身免疫性疾病在内的各种全身性疾病相关。本文报告了一名37岁患有弥漫性硬皮病的女性患者发生角层下脓疱性皮肤病的病例。鉴于我们的患者同时存在弥漫性硬皮病和角层下脓疱性皮肤病,推测免疫失调可能在角层下脓疱性皮肤病的发病机制中起作用。