IDH Mutations Are Potentially the Intrinsic Genetic Link among the Multiple Neoplastic Lesions in Ollier Disease and Maffucci Syndrome: A Clinicopathologic Analysis from a Single Institute in Shanghai, China

Background: This study aims to investigate isocitrate dehydrogenase gene mutations in patients with the non-hereditary skeletal disorders of Ollier disease and Maffucci syndrome, particularly in the extraosseous tumours. Methods: A total of 16 tumours from three patients with Ollier disease and thre...

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Detalles Bibliográficos
Autores principales: Chen, Chunyan, Li, Jian, Jiang, Ting, Tang, Juan, Zhang, Zhichang, Luo, Yanli, Wang, Xinpei, Sun, Keyang, Jiang, Zhiming, Zhou, Juan, Liu, Zhiyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9689145/
https://www.ncbi.nlm.nih.gov/pubmed/36428825
http://dx.doi.org/10.3390/diagnostics12112764

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9689145/
https://www.ncbi.nlm.nih.gov/pubmed/36428825
http://dx.doi.org/10.3390/diagnostics12112764

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