肢端持续性丘疹性黏蛋白病5例分析

发布时间：2018-11-01 12:53

【摘要】：目的:分析并总结肢端持续性丘疹性黏蛋白病(APPM)的临床、组织病理、诊断以及治疗特点。方法:回顾性分析近5年山东省皮肤病性病防治研究所诊治的5例APPM患者的临床资料。结果:5例患者手背、腕部或前臂均散在分布肤色、淡白色及淡黄色粟粒至绿豆大实性丘疹。皮损组织病理检查示表皮正常,真皮乳头及真皮网状层局部黏蛋白沉积;阿辛蓝染色证实黏液样物质沉积增多。结论:APPM是局限性黏液水肿性苔藓的一个亚型。该病临床及组织病理表现典型,一般不需要治疗。
[Abstract]:Objective: to analyze and summarize the clinical, histopathological, diagnostic and therapeutic features of (APPM). Methods: the clinical data of 5 APPM patients treated by Shandong Institute of Dermatology and venereal Disease in recent 5 years were analyzed retrospectively. Results: the skin color was scattered on the back of the hand, wrist or forearm, and millet and yellowish millet were scattered to the large solid papules of mung bean. Histopathological examination showed normal epidermis, mucin deposition in dermal papilla and dermis reticular layer, and increased deposition of mucoid substance in acinyl blue staining. Conclusion: APPM is a subtype of localized mucoedema lichen. The clinical and histopathological manifestations of the disease are typical and generally do not require treatment.
【作者单位】：山东省交通医院皮肤科;山东省皮肤病性病防治研究所;
【分类号】：R758.6

【相似文献】