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粘液水肿性苔藓3例临床病理分析 被引量:1

Clinical and Pathological Analysis on Analysis Lichen Myxedematosus of Three Cases
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摘要 粘液水肿性苔藓是一种罕见的先天性皮肤粘蛋白增多症,本科收治3例患者。男2例,女1例。临床表现主要为淡红色或近皮色粟粒大小丘疹,表面有蜡样光泽,以躯干和四肢伸侧为主。组织病理检查真皮内可见大量粘蛋白沉积。3例患者用维甲酸联合激素治疗,疗效不显著。 Lichen myxedematosus (LM) is a rare idiopathic cutaneous mucinosis, my department accepted and treated three cases of lichen myxedematosus. two were men, one was woman. The clinic feature are waxy, erythematous or flesh-colored,millet size papule,. the trunk and extremities are most frequently affected. Histological examination: Lesions have large depositions of mucin in the dermis. Three patients were treated by tretinoin in combination with corticosteroids,the curative effect was not prominent.
出处 《中国皮肤性病学杂志》 CAS 北大核心 2005年第4期234-235,共2页 The Chinese Journal of Dermatovenereology
关键词 粘液水肿性苔藓 Lichen myxedematosus
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参考文献7

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同被引文献3

  • 1Harris JE,Purcell SM,Griffin TD.Acral persistent papular mucinosis[J].J Am Acad Dermatol,2004,51(6):982-988.
  • 2Bongioletti F,Rebora A.Updated classification of papular mucinosis,lichen myxedematosus,and scleromyxedema[J].J Am Acad Dermatol,2001,44(2):273-281.
  • 3Rongioletti F.Lichen myxedematosus(papular mucinosis):new concepts and perspectives for an old disease[J].Semin Cutan Med Surg 2006,25(2):1000-1004.

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