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Recurrence in Oral Premalignancy: Clinicopathologic and Immunohistochemical Analysis
Maria Georgaki1, Dimitris Avgoustidis2, Vasileios Ionas Theofilou1,3
1Department of Oral Medicine & Pathology and Hospital Dentistry, School of Dentistry, National and Kapodistrian University of Athens, 11527 Athens, Greece.
Oral leukoplakia (OL) can recur and transform into cancer. Lower Bcl-xL and survivin levels predict recurrence, while recurrences show increased oncogenic molecule expression, suggesting distinct risk factors for recurrence versus malignant transformation.
Area of Science:
- Oral pathology
- Oncology
- Immunohistochemistry
Background:
- Oral leukoplakia (OL) frequently recurs and has potential for malignant transformation (MT).
- Predictive factors for OL recurrence and MT require further investigation.
- Understanding recurrence patterns is crucial for effective patient management.
Purpose of the Study:
- To identify sociodemographic, clinical, microscopic, and immunohistochemical predictors of OL recurrence.
- To compare primary OL lesions (PLs) with recurrent lesions.
- To analyze molecules in the STAT3 oncogenic pathway (pSTAT3, Bcl-xL, survivin, cyclin D1, Ki-67) in relation to recurrence.
Main Methods:
- Analysis of 135 OL lesions (97 PLs, 38 recurrences) from 33 patients.
- Evaluation of clinical and microscopic features, including homogeneity and dysplasia.
- Immunohistochemical analysis of STAT3 pathway molecules (pSTAT3, Bcl-xL, survivin, cyclin D1, Ki-67).
Main Results:
- Lower Bcl-xL and survivin expression were significant risk factors for OL recurrence.
- Recurrent lesions were often smaller, more homogeneous, and less dysplastic than PLs.
- Recurrences showed increased expression of pSTAT3 and Bcl-xL compared to PLs.
Conclusions:
- Distinct parameters may predict OL recurrence versus malignant transformation risk.
- Lower Bcl-xL and survivin levels are associated with increased OL recurrence.
- Excision and close monitoring are recommended for OL management, considering recurrence potential.
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