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Recurrence of a neuroendocrine tumor of adrenal origin: a case report with more than a decade follow-up
BACKGROUND: Neuroendocrine tumor (NET) with adrenocorticotropic hormone (ACTH) secretion are very rare. To our knowledge, no follow-up study is published for ACTH-secreting NET, regardless of the primary site, to show second occurrence of tumor after a long follow-up, following resection of primary...
Autores principales: | Rahmani, Fatemeh, Tohidi, Maryam, Dehghani, Maryam, Broumand, Behrooz, Hadaegh, Farzad |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791754/ https://www.ncbi.nlm.nih.gov/pubmed/33413271 http://dx.doi.org/10.1186/s12902-020-00673-7 |
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