Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility

被引:424
|
作者
Has, C. [1 ]
Bauer, J. W. [2 ,3 ]
Bodemer, C. [4 ]
Bolling, M. C. [5 ]
Bruckner-Tuderman, L. [1 ]
Diem, A. [2 ,3 ]
Fine, J-D [6 ,7 ]
Heagerty, A. [8 ]
Hovnanian, A. [9 ]
Marinkovich, M. P. [10 ]
Martinez, A. E. [11 ]
McGrath, J. A. [12 ,13 ]
Moss, C. [14 ,15 ]
Murrell, D. F. [16 ,17 ]
Palisson, F. [18 ]
Schwieger-Briel, A. [19 ]
Sprecher, E. [20 ,21 ]
Tamai, K. [22 ]
Uitto, J. [23 ]
Woodley, D. T. [24 ]
Zambruno, G. [25 ]
Mellerio, J. E. [12 ,13 ]
机构
[1] Univ Freiburg, Med Ctr, Fac Med, Dept Dermatol, Freiburg, Germany
[2] Paracelsus Med Univ Salzburg, Dept Dermatol & Allergol, Salzburg, Austria
[3] Paracelsus Med Univ Salzburg, EB Haus Austria Univ Hosp, Salzburg, Austria
[4] Univ Paris, Necker Hosp Enfants Malad, Ctr AP HP 5, Dept Dermatol, Paris, France
[5] Univ Groningen, Univ Med Ctr Groningen, Groningen, Netherlands
[6] Vanderbilt Univ, Sch Med, Nashville, TN 37212 USA
[7] Natl Epidermolysis Bullosa Registry, Nashville, TN USA
[8] Heart England Fdn Trust, Birmingham, W Midlands, England
[9] Paris Univ, Necker Hosp Sick Children, Imagine Inst, Dept Genet,INSERM,UMR1163, Paris, France
[10] Stanford Univ, Sch Med, Palo Alto Vet Affairs Med Ctr, Stanford, CA 94305 USA
[11] NHS Fdn Trust, Dermatol Dept, Great Ormond St Hosp Children, London, England
[12] Kings Coll London, St Johns Inst Dermatol, London, England
[13] Guys & St Thomas NHS Fdn Trust, London, England
[14] Birmingham Childrens Hosp, Birmingham, W Midlands, England
[15] Univ Birmingham, Birmingham, W Midlands, England
[16] St George Hosp, Sydney, NSW, Australia
[17] Univ New South Wales, Sydney, NSW, Australia
[18] Univ Desarrollo, DEBRA Chile, Fac Med, Clin Alemana, Santiago, Chile
[19] Univ Childrens Hosp Zurich, Dept Pediat Dermatol, Zurich, Switzerland
[20] Tel Aviv Univ, Tel Aviv Sourasky Med Ctr, Div Dermatol, Tel Aviv, Israel
[21] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
[22] Univ Osaka, Dermatol Dept, Osaka, Japan
[23] Thomas Jefferson Univ, Philadelphia, PA 19107 USA
[24] Univ Southern Calif, Los Angeles, CA 90007 USA
[25] Bambino Gesu Pediat Hosp, Dermatol Unit, Rome, Italy
关键词
SPLICE-SITE MUTATION; REVERTANT MOSAICISM; VII COLLAGEN; GLYCINE SUBSTITUTION; KINDLER-SYNDROME; EXTRACUTANEOUS MANIFESTATIONS; CYTOPLASMIC DOMAIN; DISEASE SEVERITY; STEM-CELLS; COL7A1;
D O I
10.1111/bjd.18921
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background Several new genes and clinical subtypes have been identified since the publication in 2014 of the report of the last International Consensus Meeting on Epidermolysis Bullosa (EB). Objectives We sought to reclassify disorders with skin fragility, with a focus onEB, based on new clinical and molecular data. Methods This was a consensus expert review. Results In this latest consensus report, we introduce the concept of genetic disorders with skin fragility, of which classicalEBrepresents the prototype. Other disorders with skin fragility, where blisters are a minor part of the clinical picture or are not seen because skin cleavage is very superficial, are classified as separate categories. These include peeling skin disorders, erosive disorders, hyperkeratotic disorders, and connective tissue disorders with skin fragility. Because of the common manifestation of skin fragility, these 'EB-related' disorders should be considered under theEBumbrella in terms of medical and socioeconomic provision of care. Conclusions The proposed classification scheme should be of value both to clinicians and researchers, emphasizing both clinical and genetic features ofEB. What is already known about this topic? Epidermolysis bullosa (EB) is a group of genetic disorders with skin blistering. The last updated recommendations on diagnosis and classification were published in 2014. What does this study add? We introduce the concept of genetic disorders with skin fragility, of which classical EB represents the prototype. Clinical and genetic aspects, genotype-phenotype correlations, disease-modifying factors and natural history of EB are reviewed. Other disorders with skin fragility, e.g. peeling skin disorders, erosive disorders, hyperkeratotic disorders, and connective tissue disorders with skin fragility are classified as separate categories; these 'EB-related' disorders should be considered under the EB umbrella in terms of medical and socioeconomic provision of care.
引用
收藏
页码:614 / 627
页数:14
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