PDF(Pubmed)
Abstract：
Sweet syndrome (SS) is a rare non-vasculitic neutrophilic dermatosis. Fever, the abrupt emergence of tender erythematous plaques and nodules, with an occasional presentation of vesicles and pustules along with dense neutrophilic infiltrates on skin biopsy are the hallmarks of the illness. Tender plaques or nodules develop along with other systemic manifestations suddenly in affected people which is considered to occur due to immune-mediated hypersensitivity. We report a case of Sweet syndrome in Pakistan presenting in a 55-year-old female. It is worth reporting due to the rarity of such cases in this region. The patient was diagnosed after profound investigations and was treated with corticosteroid therapy.
摘要：
Sweet综合征（SS）是一种罕见的非血管中性粒细胞性皮肤病。发烧,触痛的红斑和结节的突然出现，皮肤活检中偶尔出现囊泡和脓疱，以及密集的嗜中性粒细胞浸润是该病的标志。在受影响的人群中突然出现了温和的斑块或结节以及其他全身性表现，这被认为是由于免疫介导的超敏反应而发生的。我们报告了一名55岁女性在巴基斯坦出现的Sweet综合征病例。由于该地区此类案件很少见，因此值得报告。患者经过深入的调查后被诊断出，并接受了皮质类固醇治疗。
