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C型淋巴瘤样丘疹病
引用本文:郝进,刘文,邓娅. C型淋巴瘤样丘疹病[J]. 临床皮肤科杂志, 2010, 39(2)
作者姓名:郝进  刘文  邓娅
作者单位:1. 重庆医科大学附属第二医院皮肤科,重庆,400010
2. 武汉钢铁公司总医院皮肤科,湖北武汉,430080
摘    要:报告1例C型淋巴瘤样丘疹病.患者男,52岁.躯干、手腕出现丘疹及溃疡2年,反复发作,并能自愈.皮损组织病理检查:真皮全层有结节或弥漫单一异形大细胞浸润,间有少量嗜酸性粒细胞.免疫组化染色结果显示肿瘤细胞CD3、CD4、CD5、CIM5RO、CD30阳性,CD19、CD79a、CD68、CD15阴性.根据患者临床表现、组织病理检查结果和免疫表型,诊断为C型淋巴瘤样丘疹病.

关 键 词:淋巴瘤样丘疹病  C型

Lymphomatoid papulosis,subtype C:a case report
HAO Jin,LIU Wen,DENG Ya. Lymphomatoid papulosis,subtype C:a case report[J]. Journal of Clinical Dermatology, 2010, 39(2)
Authors:HAO Jin  LIU Wen  DENG Ya
Abstract:A Case of C subtype of lymphomatoid papulosis(LyP)is reported.A 52-year-old man presented with papule and ulceration for 2 years,which were recurrent and self-healing.The lesions contained a dermal infiltration composed predomi-randy of abnormal large lymphoeytes and some eosinophils.Immunohistochemical staining showed the lymphocytes were posi-tire for CD3,CD4,CD5,CIM5RO and CD30,and negtive for CDl9,CD79a,CD68 and CD15.The clinical,pathological and immunohistochemical feature of the case supported the diagnosis of C subtype of lymphomatoid papulosis.
Keywords:lymphomatoid papulosis  C subtype
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