Treatment of feet deformities in epidermolysis bullosa

被引:5
|
作者
Sternick, Marcelo Back [1 ]
Ishida Formentini, Pierina Kaneno [1 ]
Costa de Souza, Gustavo Moreira [2 ]
Teixeira, Eduardo Cembranelli [1 ]
de Almeida Filho, Ildeu Afonso [1 ]
da Costa, Sergio Moreira [2 ]
机构
[1] Hosp Felicio Rocho, Orthopaed Surg & Traumatol Dept, Belo Horizonte, MG, Brazil
[2] Hosp Felicio Rocho, Dept Plast Surg, Belo Horizonte, MG, Brazil
关键词
Epidermolysis bullosa; Foot deformities; Rare diseases; MANIFESTATIONS; MANAGEMENT;
D O I
10.1007/s00264-016-3135-1
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Background Inherited epidermolysis bullosa is a rare disease characterised by mechanical fragility of the skin when under insignificant stress. The main consequences of epidermolysis bullosa, mainly the dystrophic type, despite pseudosyndactyly, are joint contractures and deformities in hands and feet. In this study, we describe our experience treating patients suffering from epidermolysis bullosa, as far as feet deformities are concerned. Methods This is a retrospective analysis of a consecutive series of patients presenting feet deformities related to epidermolysis bullosa. Extension contractures of the toes, equinus and cavus deformities were treated with soft tissues surgery. Results Thirteen surgical procedures were done in six patients with feet deformities caused by epidermolysis bullosa. Of the feet operated 85.7 % extension contracture of the toes was asymptomatic at follow-up. However, 42.9 % developed hammertoe deformities. There were no recurrence or complications for other deformities. Subjectively, all patients declared themselves very satisfied with the results. Conclusion Foot deformities must be treated as early as possible, due to progressive disability for walking and pain symptoms. We considered that, despite long term complications, treatment was adequate and we recommend it.
引用
收藏
页码:1361 / 1365
页数:5
相关论文
共 50 条
  • [1] Treatment of feet deformities in epidermolysis bullosa
    Marcelo Back Sternick
    Pierina Kaneno Ishida Formentini
    Gustavo Moreira Costa de Souza
    Eduardo Cembranelli Teixeira
    Ildeu Afonso de Almeida Filho
    Sérgio Moreira da Costa
    [J]. International Orthopaedics, 2016, 40 : 1361 - 1365
  • [2] Treatment of Severe Hand Deformities Caused by Epidermolysis Bullosa
    Tian, Feng
    Li, Bin
    Tian, Li-Jie
    [J]. ORTHOPEDICS, 2011, 34 (11) : E780 - E783
  • [3] EPIDERMOLYSIS BULLOSA WITH CHARACTERISTIC HAND DEFORMITIES
    BRINN, LB
    KHILNANI, MT
    [J]. RADIOLOGY, 1967, 89 (02) : 272 - &
  • [4] Surgical treatment of the hand deformities in dystrophic Epidermolysis bullosa.: Case report
    Pehle, B
    Siepe, P
    Roessing, C
    von Braunmühl, N
    Safi, A
    [J]. MONATSSCHRIFT KINDERHEILKUNDE, 2001, 149 (07) : 691 - 695
  • [5] MANAGEMENT OF ADVANCED FOOT DEFORMITIES IN DYSTROPHIC EPIDERMOLYSIS BULLOSA
    RESNICK, JI
    ROHRICH, RJ
    MAY, JW
    [J]. PLASTIC AND RECONSTRUCTIVE SURGERY, 1988, 82 (05) : 888 - 891
  • [6] Treatment of epidermolysis bullosa
    Beinhauer, LG
    [J]. ARCHIVES OF DERMATOLOGY AND SYPHILOLOGY, 1935, 32 (03): : 469 - 469
  • [7] EPIDERMOLYSIS BULLOSA HEREDITARIA - REPORT OF A CASE WITH UNUSUAL ASSOCIATED DEFORMITIES
    KITLOWSKI, EA
    BANFIELD, EE
    [J]. PLASTIC AND RECONSTRUCTIVE SURGERY, 1948, 3 (04) : 481 - 488
  • [8] An algorithmic approach for the management of hand deformities in dystrophic epidermolysis bullosa
    Tuncer, Serhan
    Sezgin, Billur
    Kaya, Basar
    Ayhan, Suhan
    Latifoglu, Osman
    [J]. JOURNAL OF PLASTIC SURGERY AND HAND SURGERY, 2018, 52 (02) : 80 - 86
  • [9] RECESSIVE DYSTROPHIC EPIDERMOLYSIS-BULLOSA - MANAGEMENT OF HAND DEFORMITIES
    LETOUZE, A
    VIAU, D
    MARTIN, L
    DEPONT, P
    ROBERT, M
    [J]. EUROPEAN JOURNAL OF PEDIATRIC SURGERY, 1993, 3 (06) : 352 - 355
  • [10] SURGICAL MANAGEMENT OF HAND DEFORMITIES IN RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA
    ZAREM, HA
    PEARSON, RW
    LEAF, N
    [J]. BRITISH JOURNAL OF PLASTIC SURGERY, 1974, 27 (02): : 176 - 181