Immunohistochemical Evaluation of Ki-67 Proliferation Marker in Various Biological Variants of Ameloblastoma

TL;DR

This study compares the Ki-67 proliferation marker in different types of ameloblastoma to assess their aggressiveness and recurrence risk.

Contribution

The study provides new evidence that Ki-67 labeling index can differentiate biological behavior among ameloblastoma subtypes.

Findings

SMA had significantly higher Ki-67 LI than UA and DA.

Ki-67 LI was lowest in desmoplastic ameloblastoma.

Ki-67 LI is a reliable marker for predicting aggressiveness and recurrence in ameloblastoma.

Abstract

Introduction

Ameloblastoma remains one of the most enigmatic and locally destructive benign odontogenic tumors, posing significant therapeutic challenges owing to its variable biological behavior across histopathological subtypes. The present study aimed to evaluate and compare the proliferative activity using Ki-67 labelling index (LI) among solid/multicystic ameloblastoma (SMA), unicystic ameloblastoma (UA), and desmoplastic ameloblastoma (DA), and to correlate the findings with their known clinical aggressiveness and recurrence potential.

Materials and methods

Thirty archival formalin-fixed, paraffin-embedded blocks of ameloblastoma were retrieved. The ameloblastoma cases comprised 12 SMA (predominant plexiform pattern), 10 UA, and 08 DA cases. Four or five micrometer sections were subjected to immunohistochemical staining using a ready-to-use mouse monoclonal anti-Ki-67 antibody. Three blinded oral pathologists independently counted Ki-67-positive tumor nuclei in three hot spot high-power fields (×100), and the labelling index was calculated as the percentage of positive nuclei per 1,000 tumor cells. Data were analyzed using one-way analysis of variance (ANOVA) and Tukey’s post-hoc test; p <0.05 was considered significant.

Results

Ki-67 LI was significantly higher in SMA (mean 75.44 ± 18.58%, range 20.56-93.89%), followed by UA (22.81 ± 4.81%), and lowest in the DA (11.7 ± 15.44%; p=0.001). Post-hoc analysis confirmed significantly higher expression in SMA than in UA (p=0.001) and DA (p=0.001), with no significant difference between UA and DA (p=0.353). Excellent interobserver agreement was achieved (ICC=0.99).

Conclusion

SMA exhibited markedly higher proliferative activity than UA and DA, explaining their greater local aggressiveness and recurrence risk. The Ki-67 LI is a reliable and reproducible immunohistochemical marker that can aid risk stratification, treatment planning, and prognostic prediction in ameloblastoma.

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