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International Journal of Oral Science ; (4): 21-21, 2021.
Artículo en Inglés | WPRIM | ID: wpr-888698

RESUMEN

Ossifying fibroma (OF) and fibrous dysplasia (FD) are two fibro-osseous lesions with overlapping clinicopathological features, making diagnosis challenging. In this study, we applied a whole-genome shallow sequencing approach to facilitate differential diagnosis via precise profiling of copy number alterations (CNAs) using minute amounts of DNA extracted from morphologically correlated microdissected tissue samples. Freshly frozen tissue specimens from OF (n = 29) and FD (n = 28) patients were obtained for analysis. Lesion fibrous tissues and surrounding normal tissues were obtained by laser capture microdissection (LCM), with ~30-50 cells (5 000-10 000 µm


Asunto(s)
Humanos , Variaciones en el Número de Copia de ADN , Diagnóstico Diferencial , Fibroma Osificante/genética , Displasia Fibrosa Ósea/genética , Galactosiltransferasas , Maxilares , Recurrencia Local de Neoplasia , Proteínas Nucleares
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