Inter- and Intra-Observer Variability in Diagnosis of Oral Dysplasia
Background: Oral potentially malignant disorders (OPMDs) are lesions from which malignancy is more likely to develop that from other tissues. The potential for malignant transformation of OPMDs is estimated by determining the degree of dysplastic changes in the epithelium. Dysplasia grading has been...
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Veröffentlicht in: | Asian Pacific journal of cancer prevention : APJCP 2017-12, Vol.18 (12), p.3251-3254 |
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Zusammenfassung: | Background: Oral potentially malignant disorders (OPMDs) are lesions from which malignancy is more likely
to develop that from other tissues. The potential for malignant transformation of OPMDs is estimated by determining
the degree of dysplastic changes in the epithelium. Dysplasia grading has been criticized for lack of reproducibility
and poor predictive value but is still considered the gold standard for diagnosing OPMDs. Since grading of dysplasia
is based on architectural and cytological changes, there can be considerable inter- and intra-observer variability due
to subjective impressions. This aim in this study was to assess the degree of agreement between two pathologists
grading dysplasia in the same patients and review the existing grading system. Materials and Methods: In this
hospital-based cross-sectional study, 100 patients with clinically diagnosed OPMDs were subjected to biopsy followed
by histopathological examination. The slides were examined by two pathologists using WHO and binary systems of
classification and both were blinded to the clinical and each other’s histological diagnosis. For statistical analysis the
Chi square test was applied. Results: Statistical analysis showed poor inter-observer variability with P values of 0.8
using the WHO classification and 0.3 using the binary classification. Conclusion: Our study provides evidence that
the existing systems for grading dysplasia are not competent to rule out subjectivity. There is a need for a classification
system that can overcome this drawback. |
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ISSN: | 1513-7368 2476-762X |
DOI: | 10.22034/APJCP.2017.18.12.3251 |