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Subclinical Cushing's syndrome

Identifieur interne : 001D89 ( Main/Exploration ); précédent : 001D88; suivant : 001D90

Subclinical Cushing's syndrome

Auteurs : Michael Tsinberg [États-Unis] ; Chienying Liu [États-Unis] ; Quan-Yang Duh [États-Unis]

Source :

RBID : ISTEX:5300D73DBCC26F6BC77656733CAD3F8375E1A0F6

English descriptors

Abstract

Subclinical Cushing's syndrome (SCS) refers to subtle autonomous cortisol hypersecretion that is insufficient to generate the typical, clinically recognizable overt syndrome. Diagnosis of SCS is challenging. The combination of 1 mg overnight dexamethasone suppression test, serum ACTH level, and urinary cortisol level are used to diagnose SCS. Laparoscopic adrenalectomy is the treatment of choice for SCS. Patients with adrenal incidentalomas and SCS should be treated with perioperative steroids to prevent post‐operative hypocortisolism. J. Surg. Oncol. 2012; 106:572–574. © 2012 Wiley Periodicals, Inc.

Url:
DOI: 10.1002/jso.23143


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<term>Endocrine society</term>
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<term>Hypersecretion</term>
<term>Hypertension</term>
<term>Hypocortisolism</term>
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<div type="abstract" xml:lang="en">Subclinical Cushing's syndrome (SCS) refers to subtle autonomous cortisol hypersecretion that is insufficient to generate the typical, clinically recognizable overt syndrome. Diagnosis of SCS is challenging. The combination of 1 mg overnight dexamethasone suppression test, serum ACTH level, and urinary cortisol level are used to diagnose SCS. Laparoscopic adrenalectomy is the treatment of choice for SCS. Patients with adrenal incidentalomas and SCS should be treated with perioperative steroids to prevent post‐operative hypocortisolism. J. Surg. Oncol. 2012; 106:572–574. © 2012 Wiley Periodicals, Inc.</div>
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