摘要
临床资料患者女,32岁。因双下肢小腿伸侧反复出现红色丘疹、红斑、水疱、瘙痒20年,于2008年1月17日来我院就诊。患者20年前无明显诱因双下肢胫前出现米粒至黄豆大红色丘疹、红斑、水疱,外伤或摩擦后皮损加重,曾于多家医院诊为“湿疹”、“扁平苔藓”、“结节性痒疹”等,治疗无明显疗效。近几年水疱减少,仅出现红色丘疹,斑片,瘙痒加重,
出处
《中国麻风皮肤病杂志》
2010年第10期728-729,共2页
China Journal of Leprosy and Skin Diseases
二级参考文献11
-
1Lee JY,Pulkkinen L,Liu HS,et al.A glycine-to-arginine substitution in the triple-belical domain of type Ⅶ collagen in a family with dominant dystrophic epidermolysis bullosa pruriginosa[J].J Invest Dermatiol,1997,108(6):947-949
-
2Christiano AM,Crollick J.Pincus S,et al.Squamous cell carcinoma in a family with dominant dystrophic epidermolysis bullosa:a molecular genetic study[J].Exp Dermatol,1999,8(2):146-152
-
3Cumbiaghi S.Brusasco A,Restano L,et al.Epidermolysis bullosa pruriginosa[J].Dermatology,1997,195(1):65-68
-
4Shimizu H.Shimizu‘s Textbook of Dermatology. . 2007
-
5Pearson RW.Studies on the pathogenesis of epidermolysis bullosa. Journal of Investigative Dermatology . 1962
-
6Hintner,H,Stingl,G,Schuler,G,Fritsch,P,Stanley,J,Katz,S,Wolff,K.Immunofluorescence mapping of antigenic determinants within dermo-epidermal junction in mechanobullous diseases. Journal of Investigative Dermatology . 1981
-
7Fine JD,Bauer EA,Briggaman RA,et al.Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa.A consensus report by the Subcommittee on Diagnosis and Classification of the National Epidermolysis Bullosa Registry. Journal of the American Academy of Dermatology . 1991
-
8Fine JD,Eady RA,Bauer EA,et al.Revised classification system for inherited epidermolysis bullosa:report of the secondInternational Consensus Meeting on diagnosis and classification of epidermolysis bullosa. Journal of the American Academy of Dermatology . 2000
-
9Fine JD,Eady RA,Bauer EA,et al.The classification of inheritedepidermolysis bullosa(EB):Report of the Third International Con-sensus Meeting on Diagnosis and Classification of EB. Journal of the American Academy of Dermatology . 2008
-
10SIEGEL D H,ASHTON G H.Loss of Kindlin-1,a Human Homologof the caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112,causes Kindler syndrome. The American Journal of Human Genetics . 2003
共引文献20
-
1王连祥.痒疹样营养不良型大疱性表皮松解症继发局限性皮肤淀粉样变性1例[J].实用皮肤病学杂志,2010,3(2):110-111. 被引量:4
-
2陆原,李清,翁翊,金丽.隐性遗传营养不良型大疱性表皮松解症1例[J].实用皮肤病学杂志,2009,2(1).
-
3曹爱华,石丽君.白色丘疹样显性营养不良型大疱性表皮松解症一家系报告[J].实用皮肤病学杂志,2009,2(1):56-57.
-
4李福伦,王宏伟.胫前大疱性表皮松解症1例[J].临床皮肤科杂志,2007,36(8):513-514. 被引量:1
-
5魏志平,钟连生,刘彦群.痒疹样营养不良型大疱性表皮松解症1例[J].临床皮肤科杂志,2007,36(11):728-728. 被引量:1
-
6解士海,钱如发,蔡志凌,黄小雄,黄荣云.痒疹样营养不良型大疱性表皮松解症1例及家系调查[J].临床皮肤科杂志,2009,38(1):50-51.
-
7陈意蕾,高琳,王刚.痒疹样大疱性表皮松解症1例[J].实用皮肤病学杂志,2011,4(4):245-246.
-
8袁景桃,李俊杰,林绍华,王鲁梅,曾碧冰.痒疹样营养不良型大疱性表皮松解症1例及家系调查[J].临床皮肤科杂志,2009,38(10):661-663. 被引量:2
-
9皮肖冰,王晓霞.痒疹型营养不良性大疱性表皮松解症一家系报告[J].岭南皮肤性病科杂志,2009,16(6):401-402.
-
10印道春.营养不良型大疱性表皮松解症1例[J].中国麻风皮肤病杂志,2010,26(7):509-510. 被引量:1
-
1肖能鑫,刁庆春,柯丹.痒疹样营养不良型大疱性表皮松解症1例[J].中国麻风皮肤病杂志,2012,28(11):814-815. 被引量:1
-
2马玲,陈红英,陈柳青.痒疹样营养不良型大疱性表皮松解症1例[J].中国麻风皮肤病杂志,2012,28(8):578-579.
-
3靳培英,刘训荃.白癜风临床分型,发病与外伤的关系[J].临床皮肤科杂志,1989,18(5):235-237. 被引量:2
-
4石国光.外伤及手术并发带状疱疹10例分析[J].中国麻风皮肤病杂志,2003,19(4):366-366.
-
5遗传性皮肤病[J].中国医学文摘(皮肤科学),2014,0(3):157-157.
-
6王哲新,娄琳.420例白癜风的临床分析[J].河南大学学报(医学科学版),2002,21(2):36-37. 被引量:1
-
7张凤川,王玉凤,徐孟,汉巾煌,王郡飞.皮肤垢着病1例[J].中国麻风皮肤病杂志,2009,25(12):870-870.
-
8熊心猜,蒋献,冉玉平.锌布颗粒致幼儿大疱性表皮坏死松解型药疹2例[J].华西医学,2002,17(4):564-564.
-
9刘汉平.多发性寻常狼疮1例[J].中国皮肤性病学杂志,2011,25(10):821-821. 被引量:1
-
10鞠英,杜华,陈建民,杜养峰,何李立.梅毒误诊为股癣及湿疹1例分析[J].中国误诊学杂志,2006,6(16):3153-3153. 被引量:1