The Inflammatory Mosaic in the Histological Subtypes of Basal Cell Carcinoma

Introduction: Basal Cell Carcinoma (BCC) is defined as a slow-growing locally invasive tumor. As it spreads, it elicits a chronic inflammatory process with the recruitment of several cell types. Objective: To characterize the inflammatory infiltrate describing the different subtypes of BCC through t...

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Detalles Bibliográficos
Autores: Ramos Machado Braga, Jacqueline, Sadigursky, Moysés, de Almeida Barbosa Junior, Aryon
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2013
País:Brasil
Institución:Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)
Repositorio:Revista Brasileira de Cancerologia (Online)
Idioma:portugués
OAI Identifier:oai:rbc.inca.gov.br:article/971
Acceso en línea:https://rbc.inca.gov.br/index.php/revista/article/view/971
Access Level:acceso abierto
Palabra clave:Humanos
Neoplasias Cutâneas
Carcinoma Basocelular-fisiopatologia
Carcinoma Basocelular-patologia
Mastócitos
Humans
Skin Neoplasms
Carcinoma, Basal Cell-physiopathology
Carcinoma, Basal Cell-pathology
Mast Cells
Carcinoma Basocelular-fisiopatología
Carcinoma Basocelularfisiopatología
Mastocítos
Descripción
Sumario:Introduction: Basal Cell Carcinoma (BCC) is defined as a slow-growing locally invasive tumor. As it spreads, it elicits a chronic inflammatory process with the recruitment of several cell types. Objective: To characterize the inflammatory infiltrate describing the different subtypes of BCC through the identification and quantification of its cells. Method: This was a retrospective study of 71 paraffin blocks from patients diagnosed with non-recurrent BCC. The immunohistochemical analyses were performed using the Streptavidin-biotin-peroxidase technique (CD3, CD20, CD68, CD8, CD4, and Ki-67 cell MAST), and the toluidine blue technique for mast cells. Results: The most frequent subtypes found were infiltrating (26%) and superficial (23%) BCC. Regarding the composition of the inflammatory infiltrate, the TCD 4 + lymphocytes corresponded to the largest population (216.2 ± 22.23), followed by mast cells (111.0 ± 7.88), TCD8 + lymphocytes (57.38 ± 5.94), B lymphocytes (55.9±6.83) and macrophages (21.18 ± 2.58). The total cell proliferative activity was generally low (47.61 ± 7.48), except for more aggressive forms of the disease, in which infiltrates rich in mast cells could be found. The adenoid subtype showed a denser infiltrate, while the Cystic subtype presented a scanty infiltrate. There was an inverse relationship between the number of mast cells and the number of T lymphocytes, without correlation with aggressiveness. Conclusion: In the BCC, the peritumoral inflammatory infiltrates suggests an immune response mediated by TCD 4+ and a composition which varies according to the type of tumor. It has been suggested that the characteristics of each tumor type might reveal differences in the tumor tissue microenvironment, which cause alterations in the composition of the infiltrate, thereby favoring or impeding tumor growth.