摘要
患儿男,6个月,头面部、双上肢红斑、脓疱12 d。反射式共聚焦显微镜(RCM)检查示:棘层海绵水肿,可见脓疱样结构,真皮乳头水肿,真皮全层及毛囊周围可见大量高折光炎细胞浸润。皮损组织病理示:真皮浅中层水肿、中性粒细胞浸润及大量核尘,血管壁未见纤维蛋白样坏死。诊断:Sweet综合征。糖皮质激素治疗有效。
A 6-month-old boy presented abrupt onset of erythema and pustules on his face,head and arm for 12 days.RCM examination showed sponge edema,pustular and dermal papillary edema,a large number of hyper refractitis cells infiltrated around the dermis and hair follicles.Histopathologic examination showed the edema of upper dermis and a diffuse neutrophilic infiltration with nuclear dust in upper and middle dermis,it without fibrinoid necrosis in the vascular walls.The child was diagnosed as Sweet's syndrome.Glucocorticosteroid had a good effect.
作者
刘欣欣
毕田田
廉佳
宫泽琨
李钦峰
LIU Xinxin;BI Tiantian;LIAN Jia;GONG Zekun;LI Qinfeng(Department of Dermatology,Tianjin Children's Hospital,Tianjin 300074,China)
出处
《中国皮肤性病学杂志》
CAS
CSCD
北大核心
2020年第10期1173-1175,共3页
The Chinese Journal of Dermatovenereology