Bilateral Glandular Odontogenic Cyst of the Maxilla: A Rare Case Report and Review of Literature

##plugins.themes.academic_pro.article.main##

Abhilasha Asthana
Amit Kumar Singh
Girish Suragimath
Prasad Kulkarni
Arun Kulkarni
Anand Nimbal

Abstract

The glandular odontogenic cyst (GOC) is a recently recognized rare developmental odontogenic cyst having an aggressive behavior and accounts for 0.012 to 1.3% of all jaw cysts. In 1992, the World Health Organization recognized this cyst as glandular odontogenic cyst (GOC). Clinically, GOC usually presents as a painless, slow-growing swelling that tends to affect the anterior part of the jaws. Many authors have suggested that the cyst mainly occurs in 4th and 5th decades and presents as an expansion of jaws with or without pain or Paraesthesia. The dental professionals must be aware of the clinical significance of this lesion as the aggressive nature of the lesion has been reported and at least 25% to 55% recur following curettage. Hence the treatment of choice is excision rather than enucleation in order to obviate recurrence. Here, we report a case of bilateral GOC in the anterior region of the maxilla, in a 29-year-old male patient, which is very unusual as it is the first bilateral case to be reported in the literature.

##plugins.themes.academic_pro.article.details##

How to Cite
Asthana, A., Singh, A. K., Suragimath, G., Kulkarni, P., Kulkarni, A., & Nimbal, A. (2014). Bilateral Glandular Odontogenic Cyst of the Maxilla: A Rare Case Report and Review of Literature. International Journal of Medical and Dental Sciences, 3(2), 512–517. https://doi.org/10.19056/ijmdsjssmes/2014/v3i2/81305

References

  1. Nunn JH, Carter NE, Gillgrass TJ, Hobson RS, Jepson NJ, Meechan JG, et al. The interdisciplinary management of hypodontia: background and role of paediatric dentistry. Br Dent J 2003;194:245–51.
  2. Vieira KA, Teixeira MS, Guirado CG, Gaviao MB. Prosthodontic treatment of hypohidrotic ectodermal dysplasia with complete anodontia: case report. Quintessence Int 2007;38:75–80.
  3. Freiman A, Borsuk D, Barankin B, Sperber GH, Krafchik B. Dental manifestations of dermatologic conditions. J Am Acad Dermatol 2009;60:289–98.
  4. Berg D, Weingold DH, Abson KG, Olsen EA. Sweating in ectodermal dysplasia syndromes: A review. Arch Dermatol. 1990;126:1075–9.
  5. Tarjan I, Gabris K, Rozsa N. Early prosthetic treatment of patients with ectodermal dysplasia: A clinical report. J Prosthet Dent 2005;93:419-24.
  6. Lamartine J. Towards a new classification of ectodermal dysplasias. Clin Exp Dermatol 2003;28:351-5.
  7. Murdock S, Lee JY, Guckes A, Wright JT. A costs analysis of dental treatment for ectodermal dyslasia. J Am Dent Assoc 2005;136:1273-6.
  8. Crawford PJ, Aldred MJ, Clarke A, Tso MS. Rapp-Hodgkin syndrome: An ectodermal dysplasia involving the teeth, hair, nails and palate. Report of a case and review of the literature. Oral Surg Oral Med Oral Pathol 1989;67:50-62.
  9. Ramos V, Giebink DL, Fisher JG, Christensen LC. Complete dentures for a child with hypohidrotic ectodermal dysplasia: A clinical report. J Prosthet Dent 1995;24:32931.
  10. Jain V, Prakash H. Prosthodontic rehabilitation for ectodermal dysplasia patients. J Indian Soc Pedo Prev Dent 2000;18:54-8.