To the content
2 . 2015

Surgical treatment of hand pseudosyndactily in patient with epidermolis bullosa: clinical case and skin care

Abstract

Epidermolis bullosa (EB) – a group of rare highly polymorphic inherited disorders characterized by erosions and bullas on the skin and mucosa due to minimal exposure. Hands and feet pseudosyndactily is a severe extra-skin complication of EB which develops due to regular blistering on the hands and feet surface, and common in patients with dystrophic EB. In this manuscript we present a clinical case of effective surgical treatment of pseudosyndactily in patient with an autosomal recessive dystrophic EB, and discuss the features of post-operative and daily skin care in patients with EB.

Keywords:epidermolis bullosa, pseudosyndactily, COL7A1

Clin. Experiment. Surg. Petrovsky J. 2015. № 2. Р. 76–82.

References

1. Fine J.D., Johnson L.B., Suchindran C.M. The National Epidermolysis Bullosa Registry. J Invest Dermatol. 1994; Vol. 102: 54S–6S.

2. Fine J.D. Rare disease registries – lessons learned from the National Epidermolysis Bullosa Registry. J Rare Dis. 1996; Vol. 2: 5–14.

3. Fine J.D., Bauer E.A., McGuire J., Moshell A. Epidermolysis bullosa: clinical, epidemiologic, and laboratory advances, and the findings of the National Epidermolysis Bullosa Registry. Baltimore: Johns Hopkins University Press, 1999.

4. Fine J.D., Hintner H. Life with Epidermolysis Bullosa (EB): Etiology, Diagnosis, Multidisciplinary Care and Therapy. Wien; New York: Springer-Verlag, 2009.

5. Fine J.D., Eady R.A., Bauer E.A., et al. The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB. J Am Acad Dermatol. 2008; Vol. 58, N 6: 931–50.

6. Fine J.D., Bruckner-Tuderman L., Eady R.A., Bauer E.A., et al. Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification. J Am Acad Dermatol. 2014; Vol. 70, N 6: 1103–26.

7. Epidermolysis bullosa / Ed. J.-D. Fine, H. Hintnera; Trans. from English. ed. Yu.Yu. Kotalevskaya. Moscow: Praktika, 2014. 358 p. (in Russian)

8. Fonkalsrud E.W., Ament M.E. Surgical management of esophageal stricture due to recessive dystrophic epidermolysis bullosa. J Pediatr Surg. 1977; Vol. 12: 221–6.

9. Azizkhan R., Stehr W., Cohen A.P., et al. Esophageal strictures in children with recessive dystrophic epidermolysis bullosa: an 11-year experience with fluoroscopically guided balloon dilatation. J Pediatr Surg. 2006; Vol. 41: 55–60.

10. Ergun G.A., Lin A.N., Dannenberg A.J., Carter D.M. Gastrointestinal manifestations of epidermolysis bullosa. A study of 101 patients. Medicine (Baltimore). 1992; Vol. 71: 121–7.

11. Anderson S.H., Meenan J., Williams K.N., et al. Efficacy and safety of endoscopic dilatation of esophageal strictures in epider- molysis bullosa. Gastrointest Endosc. 2004; Vol. 59: 28–32.

12. Fine J.-D., Johnson L.B., Weiner M., Suchindran C. Gastrointestinal complications of inherited epidermolysis bullosa: cumula- tive experience of the National EB Registry. J Pediatr Gastroenterol Nutr. 2008; Vol. 46: 147–58.

13. Rodriguez-Baez N., Andersen J.M. Management of esophageal strictures in children. Curr. Treat. Options Gastroenterol. 2003; Vol. 6: 417–25.

14. Castillo R.O., Davies Y.K., Lin Y.-C., et al. Management of esophageal strictures in children with recessive dystrophic epi- dermolysis bullosa. J Pediatr Gastroenterol Nutr. 2002; Vol. 34: 535–41.

15. Heyman M.B., Zwass M., Applebaum M., et al. Chronic recurrent esophageal strictures treated with balloon dilatation in children with autosomal recessive epidermolysis bullosa dystrophica. Am. J. Gastroenterol. 1993; Vol. 88: 953–7.

16. Becker M.H., Swinyard C.A. Epidermolysis bullosa dystrophica in children: radiologic manifestations. Radiology. 1968; Vol. 90: 124–8.

17. Greider J.L.Jr, Flatt A.E. Surgical restoration of thehandin epidermolysis bullosa. Arch Dermatol. 1988; Vol. 124: 765–7.

18. Fine J.-D., Johnson L.B., Weiner M. et al Pseudosyndactyly and musculoskeletal deformities in inherited epidermolysis bullosa (EB): experience of the National EB Registry, 1986–2002. J Hand Surg (British and European Volume). 2005; Vol. 30B: 14–22.

19. Pope E., Lara-Corrales I., Mellerio J., Martinez A., et al. A consensus approach to wound care in epidermolysis bullosa. J Am Acad Dermatol. 2012; Vol. 67, N 5: 904–17.

20. El Hachem M., Zambruno G., Bourdon-Lanoy E., Ciasulli A., et al. Multicentre consensus recommendations for skin care in inherited epidermolysis bullosa. Orphanet J Rare Dis. 2014; Vol. 9: 76.

21. Mellerio J.E., Weiner M., Denyer J.E., et al. Medical management of epidermolysis bullosa: Proceedings of the 2nd international symposium on epidermolysis bullosa, Santiago, Chile, 2005. Int J Der- matol. 2007; Vol. 46: 795–800.

All articles in our journal are distributed under the Creative Commons Attribution 4.0 International License (CC BY 4.0 license)

CHIEF EDITOR
CHIEF EDITOR
Sergey L. Dzemeshkevich
MD, Professor (Moscow, Russia)

Journals of «GEOTAR-Media»