CC BY-NC-ND 4.0 · Ibnosina Journal of Medicine and Biomedical Sciences 2016; 08(04): 120-124
DOI: 10.4103/1947-489X.210224
Case Report

Ectopic ACTH syndrome caused by hepatic metastases from previously non-functional pancreatic neuroendocrine tumor

Rafik El Mehdawi
1   Department of Medicine, Faculty of Medicine, University of Benghazi, Benghazi, Libya
2   Department of Hematology and Oncology, Benghazi Medical Center, Benghazi, Libya
,
Abdulwahab Elbarsha
1   Department of Medicine, Faculty of Medicine, University of Benghazi, Benghazi, Libya
2   Department of Hematology and Oncology, Benghazi Medical Center, Benghazi, Libya
,
Najat Buzaid
1   Department of Medicine, Faculty of Medicine, University of Benghazi, Benghazi, Libya
2   Department of Hematology and Oncology, Benghazi Medical Center, Benghazi, Libya
,
Adel Attia
1   Department of Medicine, Faculty of Medicine, University of Benghazi, Benghazi, Libya
3   Department of Medicine, Benghazi Medical Center, Benghazi, Libya
,
Maisoon El Hemri
2   Department of Hematology and Oncology, Benghazi Medical Center, Benghazi, Libya
› Author Affiliations

Background: Pancreatic neuroendocrine tumors (NETs) are rare; representing less than 10% of all primary pancreatic tumors. The minority of these tumors are functional producing a clinical syndrome according to the hormone secreted. ACTH production by pancreatic NETs is rare and even rarer, it occurs from liver metastasis later in the course of the disease. Case Report: We report a case of a 30-year-old Libyan man who presented with Cushing's syndrome due to ectopic ACTH production from liver metastases of a pancreatic NET. The pancreatic NET was diagnosed 7 years previously when it was considered a nonfunctional at the time of diagnosis; the tumor was resected completely then. In the current presentation there was no evidence of the primary tumor but multiple liver metastases were present. Conclusions: This report highlights the fact that initially non-functional pancreatic NETs may present later with a functional hormonal syndrome either from the primary tumor itself or from its metastatic secondary tumors elsewhere.



Publication History

Received: 28 May 2016

Accepted: 10 June 2016

Article published online:
07 July 2022

© 2016. The Libyan Authority of Scientific Research and Technologyand the Libyan Biotechnology Research Center. All rights reserved. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License,permitting copying and reproductionso long as the original work is given appropriate credit. Contents may not be used for commercial purposes, oradapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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