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Cortisol production is normally governed by the hypothalamic–pituitary–adrenal (HPA) axis, which maintains hormonal balance through tightly regulated feedback mechanisms. Disruption of this regulatory system is central to the development of Cushing syndrome, whether the excess cortisol originates from external medications or internal pathology. Persistent cortisol elevation alters metabolism, immune function, and endocrine signaling, producing the characteristic clinical features...
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Cushing syndrome refers to the collection of clinical manifestations that arise when tissues are exposed to excessive amounts of cortisol or cortisol-like medications over an extended period. Cortisol, a glucocorticoid produced by the adrenal cortex, regulates metabolism, immune responses, and the body’s adaptation to stress. When its concentration remains chronically elevated, these physiological pathways become dysregulated, resulting in the characteristic features of the...
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Related Experiment Video

Updated: May 2, 2026

Endoscopic Endonasal Trans-sphenoidal Approach: Minimally Invasive Surgery for Pituitary Adenomas
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[Acromegaly masked by symptomatic hyperprolactinaemia].

Jakob Dal1, Charlotte Steffensen, Troels K Hansen

  • 1Medicinsk Endokrinologisk Afdeling, MEA, Aarhus Universitetshospital, Nørrebrogade 44, 8000 Aarhus C. jakob.dal@dadlnet.dk.

Ugeskrift for Laeger
|March 18, 2014
PubMed
Summary
This summary is machine-generated.

Acromegaly should be considered in patients with hyperprolactinemia and pituitary adenomas. This condition can develop over time, even with treatment for high prolactin levels.

Area of Science:

  • Endocrinology
  • Neuroendocrinology
  • Oncology

Background:

  • Pituitary macroadenomas can present with hyperprolactinemia.
  • Acromegaly is a condition characterized by excessive growth hormone production.

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  • Dopamine receptor agonists are a common treatment for hyperprolactinemia.