Draper Bradley K, Robbins Jason B, Stricklin George P
Department of Medicine, Division of Dermatology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
J Am Acad Dermatol. 2005 May;52(5):901-5. doi: 10.1016/j.jaad.2004.12.028.
Sweet's syndrome is an acute febrile neutrophilic dermatosis marked by attacks of painful, plaque-forming inflammatory papules accompanied by fever, arthralgias, peripheral leukocytosis, a diffuse dermal neutrophilic infiltrate, and prompt resolution of symptoms and lesions with glucocorticoid therapy. There are many reports of drug-induced Sweet's syndrome to various medications including all- trans -retinoic acid, carbamazepine, hydralazine, levonorgestrel/ethinyl estradiol, minocycline, trimethoprim/sulfamethoxazole, and granulocyte colony-stimulating factor. We describe the first known case of Sweet's syndrome induced by pegfilgrastim, a pegylated form of granulocyte colony-stimulating factor with unique pharmacologic properties that may induce Sweet's syndrome in patients with no history of neutrophilic dermatoses associated with granulocyte colony-stimulating factor therapy.
斯威特综合征是一种急性发热性嗜中性皮病,其特征为发作性疼痛的、形成斑块的炎性丘疹,并伴有发热、关节痛、外周血白细胞增多、弥漫性真皮嗜中性粒细胞浸润,且糖皮质激素治疗能使症状和皮损迅速消退。有许多关于多种药物诱发斯威特综合征的报道,这些药物包括全反式维甲酸、卡马西平、肼苯哒嗪、左炔诺孕酮/炔雌醇、米诺环素、甲氧苄啶/磺胺甲恶唑以及粒细胞集落刺激因子。我们描述了第一例已知由培非格司亭诱发的斯威特综合征病例,培非格司亭是一种聚乙二醇化形式的粒细胞集落刺激因子,具有独特的药理特性,可能在既往无与粒细胞集落刺激因子治疗相关的嗜中性皮病病史的患者中诱发斯威特综合征。