Title: Clinicopathological Profile and Treatment Outcomes of Ameloblastoma- A Single Institution Experience

Authors: Dr Anila. K.R., DNB (Pathology), Dr Lakshmi Rajagopal, MD (Pathology), Dr Sindhu Nair P, DNB (Pathology) , Dr Thara Somanathan, MD (Pathology), Dr Shaji Thomas, MCh, Dr Venugopal M, MD

 DOI: https://dx.doi.org/10.18535/jmscr/v9i12.27

Abstract

Introduction: Ameloblastoma is a benign slow growing tumour of odontogenic origin. How-ever, they are locally aggressive and can cause severe deformities of face. Surgery with adequate margins is the standard treatment.

Objective: This study aims to report the clinicopathologic and follow-up details of patients with ameloblastoma treated at a tertiary care centre.

Materials and Methods: This was a retrospective study where-in archived data of patients histologically diagnosed with ameloblastoma between January 2010 and December 2020 at our centre were retrieved. Information on demographic details, clinicopathologic features, treatment modality, follow‑up period, and recurrence were obtained. This study had approval of the institutional review board of our institute.

Results: A total of twenty-one patients were included in this study. Male preponderance was noted. Age predisposition was seen in the fourth decade. Most common site of involvement was posterior aspect of mandible. Most common histologic sub-type was follicular type. Radical surgery was the treatment done in most of the cases due to large size of tumour. Recurrences were noted as late as after 48 years of initial surgery.

Conclusion: Ameloblastoma though benign can attain huge sizes requiring radical surgery. Recurrences can occur many years after initial diagnosis, hence patients need to be kept on follow-up for long durations, preferably lifelong.

Keywords: Ameloblastoma, mandible, clinicopathologic features, recurrence.

References

  1. DG, Heikinheimo K, Shear M, et al. Ameloblastomas. In: Barnes L, Eveson JW, Reichart P, et al. Eds. World Health Organization Classification of Tumours. Pathology and Genetics of Head and Neck Tumours. Lyon: IARC Press, 2005:296–300.
  2. Shear M, Singh S. Age-standardized incidence rates of ameloblastoma and dentigerous cyst on the Witwatersrand, South Africa. Community Dent Oral Epidemiol 1978; 6:195–99.
  3. Oliveira LR, Matos BH, Dominguete PR, Zorgetto VA, Ribeiro-Silva A. Ameloblastoma: Report of two cases and a brief literature review. IntJ Odontostomatol 2011; 5:293-9.
  4. More C, Tailor M, Patel HJ, Asrani M, Thakkar K, Adalja C, et al.Radiographic analysis of ameloblastoma: A retrospective study.Indian J Dent Res 2012; 23:698.
  5. Kim SG, Jang HS. Ameloblastoma: A clinical, radiographic, andhistopathologic analysis of 71 cases. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2001; 91:649-53.
  6. Hasegawa T, Imai Y, Takeda D, Yasuoka D, Ri S, Shigeta T, et al. Retrospective study of ameloblastoma: The possibility of conservativetreatment. Kobe J Med Sci 2013;59: E112-21.
  7. Shoor H, Pai KM, Gupta S, Garg A, Sharma H, Kumar N. Clinical,radiographic and histopathologic features of ameloblastoma:A retrospective analysis of 21 cases. Int J Sci Stud 2014; 2:83-8.
  8. Carvalho KM, Dhupar A,Spadigam A, Syed S. Ameloblastoma: A 16-yearclinicopathological study on Goan population. Indian J Pathol Microbiol 2017; 60:157-60.
  9. Tatapudi R, Samad SA, Reddy RS, Boddu NK. Prevalence ofameloblastoma: A three‑year retrospective study. J Indian AcadOral Med Radiol 2014; 26:145.
  10. Selvamani M, Yamunadevi A, Basandi PS, Madhushankari GS.Analysis of prevalence and clinical features of multicystic ameloblastoma and its histological subtypes in South Indian sample population: A retrospective study over 13 years. J PharmBioallied Sci 014;6: S131‑4.
  11. Oomens MA, van der Waal I. Epidemiology of ameloblastomas of the jaws; a report from the Netherlands. Med Oral Patol Oral Cir Bucal 2014;19: e581‑3.
  12. Ibikunle AA, Taiwo OA,Braimah RO, Adeyemi M, Abdullahi K, Sahabi SM. Ameloblastoma: Clinicopathologic and therapeutic analysis of 67 cases seen at Usmanu Danfodiyo University Teaching Hospital Sokoto, Nigeria. Int JHealth Allied Sci 2018;7:240-5.
  13. de Moraes FB, Cardoso RM, Rodrigues SV, Dutra MV, Pereira UR,Borges TR. Ameloblastoma: A clinical and therapeutic analysis on sixcases. Rev Bras Ortop 2014; 49:305-8.
  14. Adebiyi KE, Ugboko VI, Omoniyi‑Esan GO, Ndukwe KC,Oginni FO. Clinicopathological analysis of histological variants of ameloblastoma in a suburban Nigerian population. Head FaceMed 2006; 2:42.
  15. Ladeinde AL, Ogunlewe MO, Bamgbose BO, Adeyemo WL,Ajayi OF, Arotiba GT, et al. Ameloblastoma: Analysis of 207 casesin a Nigerian teaching hospital. Quintessence Int 2006; 37:69‑74.
  16. Naik BR. Clinicopathological study of ameloblastomas: Case study intribal areas. Int J Head Neck Surg 2011; 2:1-4.
  17. McClary AC, West RB, McClary AC, Pollack JR, Fischbein NJ,Holsinger CF, et al. Ameloblastoma: A clinical review and trendsin management. Eur Arch Otorhinolaryngol 2016; 273:1649‑61.
  18. Olusanya AA, Adisa AO, Lawal AO, Arotiba JT. Gross surgical features and treatment outcome of ameloblastoma at a Nigerian tertiary hospital. Afr J Med Med Sci 2013; 42:59‑64.
  19. Dandriyal R, Gupta A, Pant S, Baweja HH. Surgical management of ameloblastoma: Conservative or radical approach. Natl J Maxillofac Surg 2011; 2:22‑7.
  20. Santos Tde S, Piva MR, Andrade ES, Vajgel A, Vasconcelos RJ, Martins‑Filho PR, et al. Ameloblastoma in the Northeast regionof Brazil: A review of 112 cases. J Oral Maxillofac Pathol2014;18: S66‑71.

Corresponding Author

Dr Anila.KR

Associate Professor, Department of Pathology, Regional Cancer Centre, Thiruvananthapuram,

Kerala-695011,India