Recurrence of a neuroendocrine tumor of adrenal origin: a case report with more than a decade follow-up

Abstract 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...

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Bibliographic Details
Main Authors: Fatemeh Rahmani, Maryam Tohidi, Maryam Dehghani, Behrooz Broumand, Farzad Hadaegh
Format: Article
Language:English
Published: BMC 2021-01-01
Series:BMC Endocrine Disorders
Subjects:
Online Access:https://doi.org/10.1186/s12902-020-00673-7