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Morphological and immunophenotypical differences between chronic periodontitis and peri-implantitis - a
European Journal of Oral Implantology
|December 14, 2017
Summary
Histopathological analysis revealed more severe inflammation and plasma cells in peri-implantitis (P-I) lesions compared to chronic periodontitis (CP). However, distinguishing between CP and P-I lesions based on these features showed poor diagnostic agreement among observers.
Area of Science:
- Oral pathology
- Periodontology
- Implant dentistry
Background:
- Chronic periodontitis (CP) and peri-implantitis (P-I) are inflammatory conditions affecting periodontal and peri-implant tissues, respectively.
- Histopathological examination is crucial for understanding disease mechanisms and differentiating between these conditions.
Purpose of the Study:
- To compare the morphology and immunophenotype of inflammatory infiltrate in CP and P-I lesions.
- To assess the diagnostic agreement among pathologists in distinguishing CP from P-I lesions based on histopathology.
Main Methods:
- Observational cross-sectional study involving 15 CP and 15 P-I gingival biopsies.
- Semiquantitative assessment of inflammatory infiltrate intensity and cellular composition (lymphocytes, plasma cells, monocytes/macrophages, granulocytes).
- Immunohistochemical analysis for CD45, CD38, CD68, myeloperoxidase (MPO)-positive cells, and vessel count.
- Evaluation of inter-observer diagnostic agreement using Kappa statistic.
Main Results:
- Peri-implantitis lesions exhibited significantly more severe inflammatory infiltrate and a higher percentage of plasma cells compared to chronic periodontitis lesions.
- Immunohistochemistry showed generally lower leukocyte subset percentages in CP (CD38: 32.05%; CD68: 6.45%; MPO: 8.62%) versus P-I (CD38: 61.13%; CD68: 9.09%; MPO: 7.47%).
- Inter-observer diagnostic agreement for differentiating CP from P-I lesions was poor to slight (Kappa = -0.18 to 0.13).
Conclusions:
- While peri-implantitis shows more severe inflammation and plasma cell infiltration, reliable differential histopathological features between CP and P-I soft-tissue lesions are difficult to establish.
- Low inter-observer agreement highlights challenges in histopathological diagnosis for distinguishing these conditions.
- Further research may be needed to identify more definitive diagnostic markers.

