摘要
<正>Laugier-Hunziker综合征(Laugier-Hunziker syndrome,LHS)是由Laugier和Hunziker两人首先报道的一种唇、口腔黏膜和指(趾)甲色素沉着性疾病。本文报道1例LHS患者。临床资料患者,女,72岁。主因发现唇部及舌体散在黑斑2月余入院。2个月前无明显诱因,患者下唇部及舌体前端出现点状或片状黑褐色斑点,后迅速增多,无任何自觉症状,无恶心、呕吐,无腹痛、便血
引文
[1] 张秀君,侯邵伟,王红梅,等.Laugier-Hunziker综合征一例[J].中国皮肤性病学杂志,2014,28(2):831-832.
[2] 赵辨.中国临床皮肤性病学[M].南京:江苏科技技术出版社,2009:1266-1267.
[3] Wang WM,Wang X,Duan N,et al. Laugier-Hunziker syndrome:a report of three cases and literature review[J].Internat J Oral Science,2013,4(4):226-230.
[4] 王翔,王文梅,高雅凡,等.Laugier-Hunziker综合征40例临床分析[J].临床口腔医学杂志,2015,11(31),674-676.
[5] Zalaudek I,Lallas A,Moscarella E,et al.The dermatologist’s stethoscope-traditional and new application of dermoscopy[J].Dermatol Pract Conc,2013,3(2):11.
[6] Ko JH,Shih YC,Chiu CS,et al.Dermoscopic features in Laugier-Hunziker syndrome[J].J Dermatol,2011,38(1):87-90.
[7] Shorning BY,Clarke AR. Energy sensing and cancer:LKB1function and lessons learnt from Peutz-Jeghers syndrome[J].Seminars Developmental Biology,2016,52:21-29.
[8] 梁岚.peutz-Jeghers综合征1例报道并浅谈[J].胃肠病学和肝病学杂志,2016,12(25):1415-1416.
[9] 李祎,樊玉.药物性色素沉着征[J],医学信息, 2011,15(9):4554.
[10] Vezzosi D,Vignaux O,Dupin N,et al.Carney complem:clinical and genetic2010 update[J].Ann Endocrinol(Paris),2010,71(6):486-493.
[11] Zuo YG,Ma DL,Jin HZ,et al.Treatment of Laugier-Hunziker syndrome with the Q-switched alexandrite laser in 22 Chinese patients[J].Arch Dermatol Res,2010,302(2):125-130.