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...

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Detalles Bibliográficos
Autores principales: Rahmani, Fatemeh, Tohidi, Maryam, Dehghani, Maryam, Broumand, Behrooz, Hadaegh, Farzad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
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

Internet

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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