Amnia for intractable skin ulcers with recessive dystrophic epidermolysis bullosa: Report of three cases

被引:16
作者
Hasegawa, Toshio [1 ]
Mizoguchi, Masayuki [1 ]
Haruna, Kunitaka [1 ]
Mizuno, Yuki [1 ]
Muramatsu, Shigenori [1 ]
Suga, Yasushi [1 ]
Ogawa, Hideoki [1 ]
Ikeda, Shigaku [1 ]
机构
[1] Juntendo Univ, Sch Med, Dept Dermatol, Bunkyo Ku, Tokyo 113, Japan
关键词
amnion; epidermolysis bullosa; skin ulcer;
D O I
10.1111/j.1346-8138.2007.00281.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Recessive dystrophic epidermolysis bullosa (RDEB) is a disease characterized by recurrent blistering and chronic ulceration of the skin. In these patients, recurrent blisters frequently result in intractable skin ulcers due to impaired wound healing caused by mutations in the type VII collagen gene and malnutrition as well as by increased collagenase activity. To evaluate the efficacy of amnia for intractable ulcers in RDEB, we treated RDEB patients with amnia. The amniotic membrane was simply placed on the cleansed wound surface. The procedure was repeated once a week for up to 10 weeks. As a result, wound conditions improved remarkably after treatment with amnia for 2-10 weeks in all the patients, resulting in total re-epithelization of the ulcers. Amnia could be an effective therapy for intractable skin ulcers in RDEB patients, and should be considered as a re-emerging therapeutic option for the disease.
引用
收藏
页码:328 / 332
页数:5
相关论文
共 29 条
[1]  
BENNETT JP, 1980, LANCET, V1, P1153
[2]  
BOSE B, 1979, ANN ROY COLL SURG, V61, P444
[4]   TREATMENT OF JUNCTIONAL EPIDERMOLYSIS-BULLOSA WITH EPIDERMAL AUTOGRAFTS [J].
CARTER, DM ;
LIN, AN ;
VARGHESE, MC ;
CALDWELL, D ;
PRATT, LA ;
EISINGER, M .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1987, 17 (02) :246-250
[5]   Biomechanical characterization of human amniotic membrane preparations for ocular surface reconstruction [J].
Chuck, RS ;
Graff, JM ;
Bryant, MR ;
Sweet, PM .
OPHTHALMIC RESEARCH, 2004, 36 (06) :341-348
[6]   FIBRONECTIN AND PROTEOGLYCANS AS DETERMINANTS OF CELL-SUBSTRATUM ADHESION [J].
CULP, LA ;
MURRAY, BA ;
ROLLINS, BJ .
JOURNAL OF SUPRAMOLECULAR STRUCTURE, 1979, 11 (03) :401-427
[7]   SUCCESSFUL ENGRAFTMENT OF CULTURED HUMAN EPIDERMAL ALLOGRAFT IN A CHILD WITH RECESSIVE DYSTROPHIC EPIDERMOLYSIS-BULLOSA [J].
EISENBERG, M ;
LLEWELLYN, DM ;
MORAN, K ;
KERR, A .
MEDICAL JOURNAL OF AUSTRALIA, 1987, 147 (10) :520-521
[8]  
FAULK WP, 1980, LANCET, V1, P1156
[9]   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 [J].
FINE, JD ;
BAUER, EA ;
BRIGGAMAN, RA ;
CARTER, DM ;
EADY, RAJ ;
ESTERLY, NB ;
HOLBROOK, KA ;
HURWITZ, S ;
JOHNSON, L ;
LIN, A ;
PEARSON, R ;
SYBERT, VP .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1991, 24 (01) :119-135
[10]   Clinical trial of allogeneic cultured dermal substitute for the treatment of intractable skin ulcers in 3 patients with recessive dystrophic epidermolysis bullosa [J].
Hasegawa, T ;
Suga, Y ;
Mizoguchi, M ;
Ikeda, S ;
Ogawa, H ;
Kubo, K ;
Matsui, H ;
Kagawa, S ;
Kuroyanagi, Y .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2004, 50 (05) :803-804