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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 被引量：4

A case of dystrophic epidermolysis bullosa puriginosa secondary to localized cutaneous amyloidosis
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摘要 临床资料患者,男,61岁。双小腿胫前起红色丘疹、结节伴瘙痒20年,偶尔出现水疱,皮损随年龄增长逐渐增多,外伤或摩擦后皮损加重,夏重冬轻。
作者 王连祥
机构地区 北京京城皮肤病医院中医皮肤科
出处 《实用皮肤病学杂志》 2010年第2期110-111,共2页 Journal of Practical Dermatology
关键词 表皮松解症 大疱性 痒疹样营养不良型 皮肤淀粉样变性
分类号 R758.59 [医药卫生—皮肤病学与性病学]
  • 相关文献

参考文献5

  • 1王刚.遗传性大疱性表皮松解症的最新分类[J].实用皮肤病学杂志,2008,1(3):129-130. 被引量：15
  • 2闫薇,王琳,冉玉平,李薇,雷观鲁.痒疹样营养不良型大疱性表皮松解症一家系调查[J].临床皮肤科杂志,2006,35(7):438-439. 被引量：8
  • 3复旦大学附属华山医院皮肤科编,王侠生.皮肤科手册[M]上海科学技术出版社,2003.
  • 4Ryynanen M,Knowlton RG,Parente MG et al.Human type Ⅶcollagen: genetic linkage of the gene(COL7A1) on chromosome 3 to dominant distrophic epidermolysis bullosa. The American Journal of Human Genetics . 1991
  • 5Hovnanian,A,Duquesnoy,O,Blanchet-Bardon,C,Knowlton,RG,Amselem,S,Lathrop,M,Dubertret,L,Uitto,J,Goossens,M.Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene. The Journal of Clinical Investigation . 1992

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

同被引文献24

  • 1李久宏,李波,宋芳吉.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,2006,22(12):1018-1019. 被引量：1
  • 2McGrath JA,Schofield OM,Eady RA. Epidermolysis bullosa pruriginosa dystrophic epidermolysis bultosa with distinctive clinicopatholgicalfeatures[J]. Br J Dermatol,1994,130(5) :617 -625.
  • 3Ee HL,Liu L,Goh CL,et al. Clinical and molecular ditemm as in the diagnosis of familial epidermolysis bullosa pmriginosa[ J ]. J Am Acad Dermatol,2007,56( 5 ) : 77 - 81.
  • 4Schumann H, Has C, Kohlhase J ,et al. Dystrophic epidermolysis bullosa pruriginosa is not associated with frequent FLG gene mutations[ J ] Br J Dermato1,2008,159 ( 2 ) : 464 - 469.
  • 5Ozanicbulic S,Fassihi H, Mellerio JE,et al. Tha lidom ide in them ana- gem ent of epidermolysis bullosa pruriginosa[ J ]Br J Dermatol,2005, 152(6) : 1332 -1334.
  • 6靳培英.皮肤病药物治疗学[M].北京:人民卫生出版社,2005.674-675.
  • 7McGrath JA, Schofield OM, Eady RA, et al. Epidennolysis bullesa pmriginosa: dystrophic epidennolysis bullosa with distinctive chnico- pathoogical features. Br J Dermalol, 1994, 130:617 - 625.
  • 8王侠生,孙新芬,方丽,等.皮肤科手册.上海:上海科学技术出版社,2003.412-413.
  • 9Almaani N, Liu L, Harrison N, et al. New glycine substitu- tion mutations in type V collagen underlying epidermoly- sis bullosa pruriginosa but the phenotype is not explained by a common ploymorphism in the matrix metalloprotein- ase- I gene promoter[ J ]. Acta Derm Venereol, 2009,89 (1) :6-11.
  • 10Drera B, Castiglia D, Zoppi N, et al. Dystrophic epider- molysis bullosa pruriginosa in Italy:clinical and molecular characterization [ J ]. Clin Genet, 2006,70 (4) : 339 -347.

引证文献4

二级引证文献4

实用皮肤病学杂志
2010年 第2期

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