Multiple unexpected lesions of metachondromatosis detected by technetium-99m methylene diphosphonate SPECT/CT: A case report

RATIONALE: Metachondromatosis (MC) is a very rare genetic disease, which is infrequently reported worldwide, which leads to osteochondroma and enchondromatosis. The disease has been shown to be associated with loss of function of the tumor suppressor gene “protein tyrosine phosphatase, non-receptor...

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Detalles Bibliográficos
Autores principales: Wang, Zi, Zou, Yuting, Chen, Yu, Chen, Yue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944487/
https://www.ncbi.nlm.nih.gov/pubmed/29703018
http://dx.doi.org/10.1097/MD.0000000000010512

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944487/
https://www.ncbi.nlm.nih.gov/pubmed/29703018
http://dx.doi.org/10.1097/MD.0000000000010512

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