Clinico-Pathologic Profile of a Cohort of Patients with Actinic Keratosis in a Tertiary Center in Romania
- PMID: 40563573
- PMCID: PMC12190252
- DOI: 10.3390/cancers17121923
Clinico-Pathologic Profile of a Cohort of Patients with Actinic Keratosis in a Tertiary Center in Romania
Abstract
Background/objectives: Actinic keratosis (AK) is considered to be the most common form of in situ carcinoma and typically arises on skin that has been chronically exposed to ultraviolet radiation. The need for early diagnosis, using non-invasive methods, has allowed for a non-surgical approach to these conditions with a significant impact on the quality of life of patients.
Methods: A retrospective study was conducted on 58 patients diagnosed with AK who underwent surgical excision at a tertiary center in Bucharest, Romania between 2018 and 2023. Clinical parameters (age, sex, lesion size, anatomical location, comorbidities) and histopathological variables (AK subtype, KIN grade, pleomorphism, solar elastosis, inflammatory infiltrate) were analyzed. Statistical associations between histological findings and clinical features were assessed using Fisher's exact test.
Conclusions: The study confirmed a predominance of AK among elderly patients, with hypertrophic lesions and moderate dysplasia (KIN II) being most common. Higher KIN grades correlated significantly with more severe pleomorphism, solar elastosis, and inflammatory response, suggesting progressive UV-induced skin damage. The findings underscore the importance of clinicopathological correlation for risk stratification and support the integration of non-invasive diagnostic tools to improve early detection and management of AK.
Keywords: actinic keratosis; epidemiology; histological subtypes; squamous cell carcinoma.
Conflict of interest statement
The authors declare no conflicts of interest.
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References
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- Stockfleth E., Ferrandiz C., Grob J.J., Leigh I., Pehamberger H., Kerl H. Development of a Treatment Algorithm for Actinic Keratoses: A European Consensus. Eur. J. Dermatol. 2008;18:651–659. - PubMed
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