Abstract
Ameloblastoma is a rare benign epithelial odontogenic neoplasm, but with great clinical implications, as despite its benignity and slow growth, most cases are locally aggressive with a significant recurrence rate. Histological, cellular, or molecular analyses of its pathogenesis have confirmed the complexity of this neoplasm. We present the case of a 20-year-old patient with a suggestive clinical and radiographic diagnosis of ameloblastoma. An incisional biopsy was obtained confirming the diagnosis of conventional ameloblastoma. Left hemimandibulectomy and plate reconstruction were performed. Histopathological analysis of the surgical specimen confirmed the conventional ameloblastoma with a plexiform pattern and significant areas of cystic degeneration and amyloid-like-like deposits. Additionally, a microarray was carried out with bioinformatic analysis for the enrichment, protein interaction, and determination of eight hub genes (CRP, BCHE, APP, AKT1, AGT, ACTC1, ADAM10, and APOA2) related to their pathogenesis.
Reference47 articles.
1. EI-Naggar, A.K., Chan, J.K.C., Grandis, J.R., Takata, T., and Slootweg, P.J. (2017). WHO Classification of Head and Neck Tumours, IARC. [4th ed.].
2. Advancements in MAPK signaling pathways and MAPK-targeted therapies for ameloblastoma: A review;You;J. Oral Pathol. Med.,2019
3. Recurrent Ameloblastoma: A surgical challenge;Aramanadka;Case Rep. Dent.,2018
4. Ameloblastoma: A succinct review of the classification, genetic understanding and novel molecular targeted therapies;Shi;Surgeon,2021
5. Ameloblastoma RNA profiling uncovers a distinct non-coding RNA signature;Davanian;Oncotarget,2017
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献