Cargando…
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...
Autores principales: | Pan, Qing, Yang, Wenbo, Zhang, Zhicai, Shao, Zengwu |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2022
|
Materias: | |
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 |
Ejemplares similares
-
Thoracic dumbbell spinal metastasis secondary to neuroendocrine tumor of unknown origin: Case report and literature review
por: Costanzo, Roberta, et al.
Publicado: (2022) -
An abdominal wall neuroendocrine tumor of unknown primary origin: A case report and review of the literature
por: Jagiella‐Lodise, Olivia, et al.
Publicado: (2022) -
Spontaneous Tumor Lysis Syndrome Secondary to Small-Cell Neuroendocrine Carcinoma of Unknown Origin: A Rare Case Report and Literature Review
por: Myint, Phyo Thazin, et al.
Publicado: (2019) -
Cutaneous Metastasis of Neuroendocrine Carcinoma with Unknown Primary Site: Case Report and Review of the Literature
por: Amorim, Gustavo Moreira, et al.
Publicado: (2015) -
Tumor‐induced Osteomalacia: A Case Report and Etiological Analysis with Literature Review
por: Zhang, Zhenhao, et al.
Publicado: (2023)