临床皮肤科杂志
臨床皮膚科雜誌
림상피부과잡지
JOURNAL OF CLINICAL DERMATOLOGY
2010年
2期
69-72
,共4页
廖文俊%樊平申%付萌%王雷%高天文
廖文俊%樊平申%付萌%王雷%高天文
료문준%번평신%부맹%왕뢰%고천문
红斑狼疮,皮肤型,线状%Blaschko线
紅斑狼瘡,皮膚型,線狀%Blaschko線
홍반랑창,피부형,선상%Blaschko선
lupus erythernatosus,cutaneous,linear%Blaschko's lines
目的:分析线状皮肤型红斑狼疮的临床表现、组织病理及免疫组化组织病理特点.方法:采用回顾性分析方法对7例线状皮肤型红斑狼绝患者的临床表现、组织病理改变、免疫荧光及实验窀检查资料进行分析.结果:7例患者中男2例,女5例;平均年龄23岁(4~40岁);平均发病年龄19.43岁(3~37岁),其中2例发病年龄<6岁.皮损部位:1例位于左下肢,其余6例均位于头面部.皮损均呈线状分布,其走向与Blasehko线一致;所有患者均无系统受累的证据.结合组织病理和免疫荧光检查,6例诊断为线状盘状红斑狼疮,1例为线状深在性红斑狼疮.结论:线状皮肤型红斑狼疮是红斑狼疮的罕见变异型,不引起系统受累.临床诊断有一定困难,需借助于组织病理和免疫荧光检查.
目的:分析線狀皮膚型紅斑狼瘡的臨床錶現、組織病理及免疫組化組織病理特點.方法:採用迴顧性分析方法對7例線狀皮膚型紅斑狼絕患者的臨床錶現、組織病理改變、免疫熒光及實驗窀檢查資料進行分析.結果:7例患者中男2例,女5例;平均年齡23歲(4~40歲);平均髮病年齡19.43歲(3~37歲),其中2例髮病年齡<6歲.皮損部位:1例位于左下肢,其餘6例均位于頭麵部.皮損均呈線狀分佈,其走嚮與Blasehko線一緻;所有患者均無繫統受纍的證據.結閤組織病理和免疫熒光檢查,6例診斷為線狀盤狀紅斑狼瘡,1例為線狀深在性紅斑狼瘡.結論:線狀皮膚型紅斑狼瘡是紅斑狼瘡的罕見變異型,不引起繫統受纍.臨床診斷有一定睏難,需藉助于組織病理和免疫熒光檢查.
목적:분석선상피부형홍반랑창적림상표현、조직병리급면역조화조직병리특점.방법:채용회고성분석방법대7례선상피부형홍반랑절환자적림상표현、조직병리개변、면역형광급실험둔검사자료진행분석.결과:7례환자중남2례,녀5례;평균년령23세(4~40세);평균발병년령19.43세(3~37세),기중2례발병년령<6세.피손부위:1례위우좌하지,기여6례균위우두면부.피손균정선상분포,기주향여Blasehko선일치;소유환자균무계통수루적증거.결합조직병리화면역형광검사,6례진단위선상반상홍반랑창,1례위선상심재성홍반랑창.결론:선상피부형홍반랑창시홍반랑창적한견변이형,불인기계통수루.림상진단유일정곤난,수차조우조직병리화면역형광검사.
Objective:To analyze the clinical,histopathologic and immunopathologic characteristics of linear cutaneous lupus erythematosus.Methods:The clinical,histopathologic,immunopathologic characteristics and laboratory examinations of 7 pa-tients with linear cutaneous lupus erythematosus were analyzed retrospectively. Results:The mean age of all cases(2 men and 5 women)was 23 years with a range from 4 to 40 years.At the onset,2 of 7 patients were under the age of 6 years,with a mean age of 19.43 years(ranging from 3 to 37 years).One patient had lesions on the left lower extremity,and six on the face and head.All patients showed a linear lesion along the lines of Blaschko,No systemic involvement has been recog-nized.Six patients were diagnosed as linear discoid lupus erythematosus,another was linear lupus erythematosus profundus,according to the clinical,histopathologic and immunopathologic features.Conclusions:Linear cutaneous lupus erythematosusis a rare variant of lupus erythematosus.No systemic involvement was documented.The clinical diagnosis of linear cutaneous lupus erythematosus may be difficult.The histopathologic and immunopathologic features are helpful to confirm the diagnosis.