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Overview of the 2022 WHO Classification of Adrenal Cortical Tumors
Endocrine Pathology, 2022 The new WHO classification of adrenal cortical proliferations reflects translational advances in the fields of endocrine pathology, oncology and molecular biology.
Ronald R de Krijger +2 more
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Nature Reviews Disease Primers, 2021
Adrenal insufficiency can arise from a primary adrenal disorder, secondary to adrenocorticotropic hormone deficiency, or by suppression of adrenocorticotropic hormone by exogenous glucocorticoid or opioid medications.
Wiebke Arlt +2 more
exaly +3 more sources
Adrenal insufficiency can arise from a primary adrenal disorder, secondary to adrenocorticotropic hormone deficiency, or by suppression of adrenocorticotropic hormone by exogenous glucocorticoid or opioid medications.
Wiebke Arlt +2 more
exaly +3 more sources
Endocrine Reviews, 2020 An adrenal incidentaloma is now established as a common endocrine diagnosis that requires a multidisciplinary approach for effective management. The majority of patients can be reassured and discharged, but a personalized approach based upon image ...
Rosemary Dineen +2 more
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New England Journal of Medicine, 2019 Glucocorticoid replacement therapy, available since the 1950s, has prolonged the survival of patients with adrenal insufficiency.1 However, adrenal crises, which are life-threatening medical emergencies, still develop in many affected patients.
David J Torpy +2 more
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Adrenal insufficiency: physiology, clinical presentation and diagnostic challenges.
Clinica chimica acta; international journal of clinical chemistry, 2020Adrenal insufficiency (AI) is a serious condition, which can arise from pathology affecting the adrenal gland itself (primary adrenal insufficiency, PAI), hypothalamic or pituitary pathology (secondary adrenal insufficiency, SAI), or as a result of ...
J. Martin-Grace +3 more
semanticscholar +1 more source
Congenital Adrenal Hyperplasia
Journal of Pediatric and Adolescent Gynecology, 2017The congenital adrenal hyperplasias (CAH) comprise a family of autosomal recessive disorders that disrupt adrenal steroidogenesis. The most common form is due to21-hydroxylase deficiency associated with mutations in the CYP21A2 gene which is located at ...
S. Witchel
semanticscholar +1 more source
Hypothalamic-pituitary-adrenal axis, neuroendocrine factors and stress.
Journal of Psychosomatic Research, 2002C. Tsigos, G. Chrousos
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