Long-Term Follow-Up of Significant Improvement After CAPTEM Treatment for Rare Adrenocorticotropin-Producing Cardiac Neuroendocrine Tumor

Long-Term Follow-Up of Significant Improvement After CAPTEM Treatment for Rare Adrenocorticotropin-Producing Cardiac Neuroendocrine Tumor

Ectopic adrenocorticotropic hormone (ACTH) syndrome (EAS) is a rare cause of Cushing syndrome. If routine imaging examinations cannot identify the source of ACTH production, long-term follow-up observation is necessary to determine the etiology. We present the case of a middle-aged male with gradual...

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Bibliographic Details
Main Authors: Lin Lu, Qingqing Meng, Xiaoping Xing, Tao Yuan, Huabing Zhang, Naishi Li, Yining Wang, Yuejuan Cheng, Chunmei Bai, Hao Wang, Xin Cheng, Yu Xiao, Boju Pan, Yuan Li, Jian Sun, Zhiyong Liang, Huijuan Zhu, Renzhi Wang, Zhaolin Lu
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-10-01
Series:Frontiers in Endocrinology
Subjects:
Cushing syndrome
ACTH syndrome
ectopic
cardiac neoplasms
neuroendocrine tumor
chemotherapy
Online Access:https://www.frontiersin.org/article/10.3389/fendo.2019.00713/full

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https://www.frontiersin.org/article/10.3389/fendo.2019.00713/full

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