Cushing's Syndrome Accompanied with Adrenal and Pancreatic Mass: A Case Report

A Amouzegar; A Ghanei; F Azizi

International Journal of Endocrinology and Metabolism

Research Institute for Endocrine Sciences

Current Issue All Issues In Press Search

Journal Information Boards and Committees Indexing and Listing Sources Journal Metrics Open Peer Review (OPR)Publication Ethics and Malpractice Statement Reviewer and AE Registration Form Support Contact Us

APC

Authors Guide Submit Manuscript

Cushing's Syndrome Accompanied with Adrenal and Pancreatic Mass: A Case Report

Author(s):

A Amouzegar

^1,*,

A Ghanei²,

F Azizi²

1Endocrine Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University (MC), [email protected], IR.Iran

2Endocrine Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University (MC), IR.Iran

International Journal of Endocrinology and Metabolism:Vol. 6, issue 3; 154-157

Published online:Jul 31, 2008

Article type:Case Report

Received:Jan 26, 2008

Accepted:Aug 04, 2008

How to Cite:Amouzegar A, Ghanei A, Azizi F. Cushing's Syndrome Accompanied with Adrenal and Pancreatic Mass: A Case Report. Int J Endocrinol Metab. 2008;6(3):. doi:

Abstract

Cushing's syndrome results from inappropriate excessive endogenous glucocorticoids secretion. It may be due to ACTH-producing pituitary adenoma, Adrenocortical adenoma, iatrogen glu-cocorticoid use, or ectopic ACTH production. Pa-tients, who remain untreated, have high morbid-ity and a significant mortality. We describe a very challenging case of Cushing's syndrome due an adrenal adenoma on a pancreatic mass. Material and Methods: A 20-year-old woman presented with sign and symptoms of Cushing syndrome. Thorough basal and dynamic hor-monal assessment. In addition, the results of im-aging studies are presented. Results: The source of ACTH secretion was adrenal adenoma, and hypercortisolism was con-trolled by adrenalectomy. A unique feature of this case is the fact that we observed an adrenal adenoma as a source of Cushing syndrome and an incidental nonfunctional pancreatic nesidiob-lastosis. Conclusion: The diagnosis of Cushing's syn-drome may turn out to be sometimes a complex and time-consuming challenge in clinical endo-crinology.

Keywords

Cushing's syndrome

Pancreatic tu-mor

Full Text

Full text is available in PDF

Import into EndNote Import into BibTex

Share on

Comments

Number of Comments:0

Cited by

Scopus by DOI: 0
Last Update: 4 days ago
Scopus by Title: 0
Last Update: 4 days ago
Scopus by Title (Ref): 0
Last Update: 4 days ago
CrossRef: 0
Last Update: 1 day ago

Metrics

Ordering Reprints

Articles are published under the Creative Commons license stated on each article. No permission or royalty fee is required for uses permitted by that license. CCC handles optional bulk and customized reprint orders. Any quotation covers production and delivery services only, not copyright permission. > Request Reprints from CCC

Search Relations

Author(s):

A Amouzegar:[PubMed][Scholar]
A Ghanei:[PubMed][Scholar]
F Azizi:[PubMed][Scholar]

Research Institute for Endocrine Sciences

Outlines

Cushing's Syndrome Accompanied with Adrenal and Pancreatic Mass: A Case Report

Abstract

Full Text

Last Update: 4 days ago

Last Update: 4 days ago

Last Update: 4 days ago

Last Update: 1 day ago