medigraphic.com
ISSN 2395-9215 (Print)
Órgano Oficial de Difusión de la Facultad de Odontología de la UNAM

2014, Number 2

<< Back Next >>

Rev Mex Ortodon 2014; 2 (2)

Stomatologic management of dental malocclusion in patients with dystrophic epidermolysis bullosa using an interceptive guide of occlusion (IGO): Comparison of two cases

Portillo NE, de la Teja ÁE, Durán GA

Language: Spanish
References: 25
Page: 114-121
PDF size: 524.18 Kb.


ABSTRACT

Epidermolysis bullosa is a genetic syndrome that consists in the formation of blisters on the skin and oral epithelium in response to mechanical trauma. Epidermolysis bullosa is classified into three major categories, including epidermolysis bullosa simplex, junctional epidermolysis bullosa, and dystrophic epidermolysis bullosa. The dental treatment of patients with epidermolysis bullosa represents a challenge due to the difficulty of operative techniques and the risk of causing blisters in the oral mucosa and also because of the microstomia that results from the cicatrization of injuries in oral epithelium. The pediatric dentist should treat the patient with an integral approach not only by means of restauration or mutilatory treatments, but including an individual risk analysis and prediction for the long term to guide the patient to an excellent status of oral health.


REFERENCES

  1. Wright T, Fine J, Jonhson L. Hereditary epidermolysis bullosa: oral manifestations and dental management. Pediatr Dent. 1993; 15: 242-247.

  2. Baquero-Fernández M, Herrera-Ceballos E, López J, De Lucas R, Romero J, Serrano M et al. Guía de atención clínica integral para la epidermólisis bullosa hereditaria. Madrid: Ministerio de Sanidad y Consumo de Madrid, Centro de Publicaciones; 2008. pp. 33-43.

  3. Fine JD, Eady RA, Bauer EA, Bauer JW, Bruckner-Tuderman L, Heagerty 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; 58: 931-950.

  4. Salas-Alanis J, McGrath J. Las epidermólisis bullosas distróficas en México: 2470insG representa la mutación más común en 21 familias. Gac Méd Méx. 2006; 142 (1): 242-248.

  5. Lanier P, Posnick W, Donly K. Epidermolysis bullosa dental management and anesthesic considerations: case report. Pediatr Dent. 1994; 12 (4); 246-249.

  6. Rathna V, Rekka P, Ramesh S, Swathi S. Dental and anesthesic management of a child with epidermolysis bullosa. J Ind Soc Ped Prev Dent. 2011; 29 (2): 155-160.

  7. Torres CP, Gomes-Silva JM, Mellara TS, Carvalho LP, Borsatto M. Dental care management in a child with recessive dystrophic epidermolysis bullosa. Braz Dent J. 2011; 22 (6): 511-516.

  8. Harris J, Bryan R, Lucas V, Roberts G. Dental disease and caries related microflora in children with dystrophic epidermolysis bullosa. Pediatr Dent. 2001; 23: 438-443.

  9. Eswara U. Dystrophic epidermolyisis bullosa in a child. Contemp Clin Dent. 2012; 3: 90-92.

  10. Wright J, Gantt D. Epidermolysis bullosa associated with enamel hypoplasia and taurodontism. Jour of Oral Path Med. 1983; 12 (2): 73-83.

  11. Al-Jobeir A. Hereditary epidermolysis bullosa: report of two cases. Saudi Dent Journ. 2006; 18 (3).

  12. Espinosa-Ortega S, Cadena-Galdós A. Epidermólisis bullosa. Reporte de caso. Rev AMOP. 1995; 7 (2): 5-9.

  13. García M, Reyes O, López J, Márquez L, Bojorquez Y. Epidermólisis bullosa distrófica: reporte de un caso clínico. Oral. 2012; 42: 902-905.

  14. Takane-Torres JM, Álvarez-Aguirre ML, Daza-García RE, Blancas-Mendoza YL. Epidermólisis ampollar distrófica. Presentación de un caso. Rev ADM. 2012; 69 (2): 83-90.

  15. Kramer S, Serrano M, Zillmann G, Galvez P, Araya I, Yanine N et al. Oral health care for patients with epidermolysis bullosa – best clinical practice guidelines. Inter Jour Paediat Dent. 2012; 22: 1-35.

  16. Rigoni-Gürtler T, Martins-Diniz L, Filho JB. Recessive dystrophic epidermolysis bullosa mitis. Case report. An Bras Dermatol. 2005; 80 (5): 503-508.

  17. Wright JT, Fine JD, Johnson L. Oral soft tissues in hereditary epidermolysis bullosa. Oral Surg Oral Med Oral Pathol. 1991; 71: 440-446.

  18. Wright JT, Fine JD, Johnson L. Dental caries in hereditary epidermolysis bullosa. Pediatr Dent. 1994; 16: 427-432.

  19. Wright JT. Comprehensive dental care and general anaesthetic management of hereditary epidermolysis bullosa. A review of fourteen cases. Oral Surg Oral Med Oral Pathol. 1990; 70: 573-578.

  20. Fine JD, Mellerio J. Extracutaneous manifestations and complications of inherited epidermolysis bullosa. Part I. Epithelial associated tissues. J Am Acad Dermatol. 2009; 61: 367-384.

  21. Fine JD, Mellerio J. Extracutaneous manifestations and complications of inherited epidermolysis bullosa. Part II. Other organs. J Am Acad Dermatol. 2009; 61: 387-402.

  22. Featherstone J, Domejean-Orliaguet S. Caries risk assesment in practice for age 6 through adult. CDA Journ. 2007; 35: 703-713.

  23. Dale J. JCO interviews: Jack Dale on serial extraction. Part 3. Journal Clin Ortho. 1976; 3: 196-217.

  24. Kjellgren B. Serial extraction as a corrective procedure in dental orthopaedic therapy. European Journal of Orthodontics. 2007; 29: 323-325.

  25. Shah H, McDonald F, Lucas V, Ashley P, Roberts G. A cephalometric analysis of patients with recessive dystrophic epidermolysis bullosa. The Angle Orthodontist. 2002; 72 (1): 55-60.




2020     |     www.medigraphic.com