Epibulbar osseous choristoma: Two case reports

BACKGROUND: Choristoma is a rare, benign, congenital proliferative tumor, with osseous choristoma being the rarest. Although the tumor is benign, effective identification is needed for its diagnosis and treatment. Here, we report the diagnosis and successful surgical treatment of two patients with o...

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Detalles Bibliográficos
Autores principales: Wang, Yu-Chen, Wang, Zi-Zhen, You, De-Bo, Wang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790453/
https://www.ncbi.nlm.nih.gov/pubmed/35127924
http://dx.doi.org/10.12998/wjcc.v10.i3.1093

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790453/
https://www.ncbi.nlm.nih.gov/pubmed/35127924
http://dx.doi.org/10.12998/wjcc.v10.i3.1093

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