Rare Bone Metastasis of Neuroendocrine Tumors of Unknown Origin: A Case Report and Literature Review

BACKGROUND: The neuroendocrine tumor (NET) is rare, accounting for about 0.5% of all tumors. NETs have the characteristics of metastasis, especially lymph nodes, liver, spleen, and bone. CASE PRESENTATION: We report a 30‐year‐old man diagnosed with a NET with bone metastasis and presented with waist...

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Detalles Bibliográficos
Autores principales: Pan, Qing, Yang, Wenbo, Zhang, Zhicai, Shao, Zengwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2022
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9531072/
https://www.ncbi.nlm.nih.gov/pubmed/35856167
http://dx.doi.org/10.1111/os.13384

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9531072/
https://www.ncbi.nlm.nih.gov/pubmed/35856167
http://dx.doi.org/10.1111/os.13384

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