Predictors of local invasion in infiltrative basal cell carcinoma: tumour budding outperforms the WHO subtyping
Autor/a
Fecha de publicación
2024ISSN
1651-2057
Resumen
Tumour budding (TB) correlates with increased local invasion in various neoplasms. Certain basal cell carcinomas (BCCs) exhibit local aggressiveness. Detecting adverse prognostic factors in partial biopsies could aid in identifying cases with heightened local risk. The absolute number of TB (≤ 3 tumour cells) in excision specimens of 271 infiltrative BCCs (0: absent; 1: 1–2 foci; 2: ≥ 3 foci; 3: ≥ 10 foci), the histopathological subtype and depth of infiltration, perineural invasion, and other histological features were evaluated. A significant correlation was found between TB and both depth of infiltration (rho 0.445, p < 0.001) and perineural invasion (p = 0.009). In the multivariate analysis of depth and perineural invasion (multiple regression, stepwise), TB was identified as a significant covariate together with diameter, inflammation, and perineural invasion for the former, and depth for the latter. Conversely, no correlation existed between the WHO histological subtypes (infiltrating, sclerosing, and micronodular), and depth of infiltration or perineural invasion. This study demonstrates the value of TB as a biomarker for local invasiveness in BCC. In routine practice, a count of ≥ 3 TB foci in lesions incompletely excised or with narrow tumour-free surgical margins would be a straightforward and reproducible method to guide BCC treatment.
Tipo de documento
Artículo
Versión del documento
Versión publicada
Lengua
Inglés
Materias (CDU)
61 - Medicina
616 - Patología. Medicina clínica. Oncología
Palabras clave
Páginas
6
Publicado por
Medical Journals Sweden
Colección
104
Publicado en
Acta Dermato-Venereologica
Citación recomendada
Fernandez Figueras, Maria Teresa; Perez Muñoz, Noelia; Puig, Luis [et al.]. Predictors of local invasion in infiltrative basal cell carcinoma: tumour budding outperforms the WHO subtyping. Acta Dermato-Venereologica, 2024, 104, adv40172. Disponible en: <https://medicaljournalssweden.se/actadv/article/view/40172>. Fecha de acceso: 17 dic. 2024. DOI: 10.2340/actadv.v104.40172
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