【摘要】：目的:分析并總結(jié)肢端持續(xù)性丘疹性黏蛋白病(APPM)的臨床、組織病理、診斷以及治療特點。方法:回顧性分析近5年山東省皮膚病性病防治研究所診治的5例APPM患者的臨床資料。結(jié)果:5例患者手背、腕部或前臂均散在分布膚色、淡白色及淡黃色粟粒至綠豆大實性丘疹。皮損組織病理檢查示表皮正常,真皮乳頭及真皮網(wǎng)狀層局部黏蛋白沉積;阿辛藍染色證實黏液樣物質(zhì)沉積增多。結(jié)論:APPM是局限性黏液水腫性苔蘚的一個亞型。該病臨床及組織病理表現(xiàn)典型,一般不需要治療。
[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.
【作者單位】： 山東省交通醫(yī)院皮膚科;山東省皮膚病性病防治研究所;
【分類號】：R758.6

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