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      Distinguishing Cushing's disease from the ectopic ACTH syndrome: Needles in a haystack or hiding in plain sight?

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          Abstract

          In the context of ACTH‐dependent Cushing's syndrome, ectopic ACTH secretion from a neuroendocrine tumour is not uncommon, and needs to be carefully differentiated from pituitary‐dependent Cushing's syndrome, Cushing's disease, in order to optimise therapy. Some cases may be quite obvious, while in others the diagnosis may be difficult to confirm and the source of ACTH problematic, as many clinical and biochemical tests may overlap with Cushing's disease. Imaging is essential, but needs to be interpreted in the light of both anatomical as well as functional imaging modalities. In this review we summarise some of the main diagnostic problems, and emphasise the multimodal and interdisciplinary nature of the diagnostic pathways.

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          Cushing's syndrome.

          Cushing's syndrome results from lengthy and inappropriate exposure to excessive glucocorticoids. Untreated, it has significant morbidity and mortality. The syndrome remains a challenge to diagnose and manage. Here, we review the current understanding of pathogenesis, clinical features, diagnostic, and differential diagnostic approaches. We provide diagnostic algorithms and recommendations for management.
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            Cushing's syndrome.

            Chronic exposure to excess glucorticoids results in diverse manifestations of Cushing's syndrome, including debilitating morbidities and increased mortality. Genetic and molecular mechanisms responsible for excess cortisol secretion by primary adrenal lesions and adrenocorticotropic hormone (ACTH) secretion from corticotroph or ectopic tumours have been identified. New biochemical and imaging diagnostic approaches and progress in surgical and radiotherapy techniques have improved the management of patients. The therapeutic goal is to normalise tissue exposure to cortisol to reverse increased morbidity and mortality. Optimum treatment consisting of selective and complete resection of the causative tumour is necessay to allow eventual normalisation of the hypothalamic-pituitary-adrenal axis, maintenance of pituitary function, and avoidance of tumour recurrence. The development of new drugs offers clinicians several choices to treat patients with residual cortisol excess. However, for patients affected by this challenging syndrome, the long-term effects and comorbidities associated with hypercortisolism need ongoing care.
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              Consensus on diagnosis and management of Cushing's disease: a guideline update

              Cushing's disease requires accurate diagnosis, careful treatment selection, and long-term management to optimise patient outcomes. The Pituitary Society convened a consensus workshop comprising more than 50 academic researchers and clinical experts to discuss the application of recent evidence to clinical practice. In advance of the virtual meeting, data from 2015 to present about screening and diagnosis; surgery, medical, and radiation therapy; and disease-related and treatment-related complications of Cushing's disease summarised in recorded lectures were reviewed by all participants. During the meeting, concise summaries of the recorded lectures were presented, followed by small group breakout discussions. Consensus opinions from each group were collated into a draft document, which was reviewed and approved by all participants. Recommendations regarding use of laboratory tests, imaging, and treatment options are presented, along with algorithms for diagnosis of Cushing's syndrome and management of Cushing's disease. Topics considered most important to address in future research are also identified.
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                Author and article information

                Contributors
                aimee.hayes@nhs.net
                Journal
                J Neuroendocrinol
                J Neuroendocrinol
                10.1111/(ISSN)1365-2826
                JNE
                Journal of Neuroendocrinology
                John Wiley and Sons Inc. (Hoboken )
                0953-8194
                1365-2826
                18 August 2022
                August 2022
                : 34
                : 8 , Cushing's Syndrome: one hundred years after Minnie G ( doiID: 10.1111/jne.v34.8 )
                : e13137
                Affiliations
                [ 1 ] Neuroendocrine Tumour Unit, ENETS Centre of Excellence Royal Free Hospital London UK
                [ 2 ] Centre for Endocrinology Barts and the London School of Medicine London UK
                [ 3 ] Green Templeton College University of Oxford Oxford UK
                Author notes
                [*] [* ] Correspondence

                Aimee R. Hayes and Ashley B. Grossman, Neuroendocrine Tumour Unit, Royal Free Hospital, Pond Street, London NW3 2QG, UK.

                Email: aimee.hayes@ 123456nhs.net and ashley.grossman@ocdem.ox.ac.uk

                Author information
                https://orcid.org/0000-0003-4417-7716
                https://orcid.org/0000-0003-1176-6186
                Article
                JNE13137
                10.1111/jne.13137
                9542389
                35980277
                a97ff788-0b9f-482c-a28d-6c55061fc090
                © 2022 The Authors. Journal of Neuroendocrinology published by John Wiley & Sons Ltd on behalf of British Society for Neuroendocrinology.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 02 March 2022
                : 11 January 2022
                : 25 March 2022
                Page count
                Figures: 2, Tables: 0, Pages: 8, Words: 6779
                Categories
                Editor Invited Review
                Editor Invited Review
                Custom metadata
                2.0
                August 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.0 mode:remove_FC converted:07.10.2022

                Endocrinology & Diabetes
                acth,carcinoid,cushing's,diagnosis,ectopic,neuroendocrine tumour
                Endocrinology & Diabetes
                acth, carcinoid, cushing's, diagnosis, ectopic, neuroendocrine tumour

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