摘要
患者女,65岁。双下肢红褐色斑疹反复1年余。实验室检查血沉增快、血球蛋白增高,类风湿因子阳性;抗核抗体、抗SS-A、抗SS-B及抗RO-52阳性。皮损病理活检示表皮大致正常;真皮血管壁增厚,周围淋巴细胞浸润。诊断:高球蛋白血症性紫癜合并干燥综合征。
A 65-year-old woman presented with reddish brown maeules on her legs for 1 year. Laboratory examination showed increased erythrocyte sedimentation rate and plasma globulin levels, RF-positive, positive for ANA, anti SS-A,anti SS-B, and anti Ro-52. Histopathology examination of skin lesion showed normal epidermis, vascular wall thickening and perivascular lymphocytic infiltration. The diagnosis of hyperglobulinemic purpura complicated by Sj-gren syndrome was made.
出处
《中国皮肤性病学杂志》
CSCD
北大核心
2017年第12期1355-1356,共2页
The Chinese Journal of Dermatovenereology
