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作 者:王小坡[1] 温斯健[1] 姜祎群[1] 杨莹[1] 孙建方[1] WANG Xiao-po WEN Si-jian JIANG Yi-qun YANG Ying SUN Jian-fang(Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing 210042, China)
机构地区:[1]中国医学科学院北京协和医学院皮肤病医院病理科,江苏南京210042
出 处:《中国皮肤性病学杂志》2016年第10期1040-1041,共2页The Chinese Journal of Dermatovenereology
摘 要:患者女,58岁。面颈部橘红色斑块5年。皮肤科情况:面部。尤其右眼眶周围和颈部融合性橘红色斑块、结节。皮损边界清楚,部分皮疹边缘可见红晕。血清免疫电泳示单克隆IgG k轻链。组织病理:表面萎缩变薄,真皮全层弥漫性组织细胞,泡沫细胞及多核巨细胞浸润,部分区域可见散在淋巴细胞浸润,未见明显渐进性坏死。诊断为无渐进坏死性黄色肉芽肿伴IgG κ型副球蛋白血症。A 58-year-old woman suffered progressive red-orange nodules and plaques involving the face and neck for 5 years. Physical examination revealed indurated red-orange nodules and plaques with erythematous borders covering the face (especially the right periorbital areas ) and the neck. A monoclonal IgG kappa light chains were detected by serum protein immunoelectrophoresis. Histologic examination revealed dense infiltrates of macrophages with some foreign-body-type giant cell and foamy macrophages were accompanied by a moderate lymphocytic cells. However, evident zones of degenerated collagen and cholesterol clefts were missing. A diagnosis of nonnecrobiotic necrobiotic xanthogranuloma with immunoglobulin G kappa paraproteinemia was made.
分 类 号:R758.6[医药卫生—皮肤病学与性病学]
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