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Cushing's disease: pathobiology, diagnosis, and management
Open accessAbstract
Cushing's disease (CD) is the result of excess secretion of adrenocorticotropic hormone (ACTH) by a benign monoclonal pituitary adenoma. The excessive secretion of ACTH stimulates secretion of cortisol by the adrenal glands, resulting in supraphysiological levels of circulating cortisol. The pathophysiological levels of cortisol are associated with hypertension, diabetes, obesity, and early death. Successful resection of the CD-associated ACTH-secreting pituitary adenoma is the treatment of choice and results in immediate biochemical remission with preservation of pituitary function. Accurate and early identification of CD is critical for effective surgical management and optimal prognosis. The authors review the current pathophysiological principles, diagnostic methods, and management of CD.
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“Cushing disease, the most common cause of ACTH-dependent CS accounting for approximately 80% of cases, occurs when a pituitary adenoma secretes ACTH, which in turn stimulates supraphysiologic secretion of cortisol from the adrenal glands (2, 4, 5, 73).”
From Approach to the Patient: Diagnosis of Cushing Syndrome (2022) · cites this paper as [73]
In the citing paper
“Cushing disease, the most common cause of ACTH-dependent CS accounting for approximately 80% of cases, occurs when a pituitary adenoma secretes ACTH, which in turn stimulates supraphysiologic secretion of cortisol from the adrenal glands (2, 4, 5, 73).”
From Approach to the Patient: Diagnosis of Cushing Syndrome (2022) · cites this paper as [73]
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“72 surgical treatment selective adenomectomy Successful adenomectomy eradicates the ACTH-secreting adenoma and immediately eliminates excess cortisol production while maintaining normal pituitary function (Fig.”
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“After the isolation, sequencing, and synthesis of CRH by Vale and colleagues in 1983, 106 CRH stimulation was introduced as a diagnostic test for the differential diagnosis of ACTH-dependent causes of CS (Fig.”
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“Cushing disease, the most common cause of ACTH-dependent CS accounting for approximately 80% of cases, occurs when a pituitary adenoma secretes ACTH, which in turn stimulates supraphysiologic secretion of cortisol from the adrenal glands (2, 4, 5, 73).”
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Metadata
- Authors
- Lonser, R. R., Nieman, L., & Oldfield, E. H.
- Affiliations
- The Ohio State University Wexner Medical Center (US)
- National Institutes of Health (US)
- University of Virginia Health System (US)
- Corresponding author
- Lonser, Russell R.
- Venue
- Journal of Neurosurgery
- Published
- 2017-02
- Volume
- 126
- Issue
- 2
- Pages
- 404-417
- ISSN
- 0022-3085 (ISSN-L)
- 1933-0693
- OpenAlex
- W2340359999
- Cited by
- 215
- References
- 0
- Citations by year
- 2026: 16 · 2025: 27 · 2024: 19 · 2023: 25 · 2022: 33 · 2021: 25 · 2020: 21 · 2019: 18 · 2018: 16 · 2017: 11
- FWCI
- 2.35
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of neurosurgery (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Pituitary Gland Disorders and Treatments
- Health Sciences › Medicine › Surgery › Adrenal and Paraganglionic Tumors
- Health Sciences › Medicine › Oncology › Neuroendocrine Tumor Research Advances
- Keywords
- Cushing's disease, hypercortisolism, cortisol excess, hypertension, diabetes mellitus, obesity, pituitary surgery, biochemical remission, diagnosis, pathophysiology
- MeSH terms
- Humans, Pituitary ACTH Hypersecretion
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