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Barts and the London School of Medicine, Centre for Endocrinology, William Harvey Institute, London, UK
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Obesity, Type 2 Diabetes and Immunometabolism Research Group, School of Cardiovascular and Metabolic Medicine & Sciences, Faculty of Life Course Sciences, King’s College London, London, UK
Division of Reproductive Health, Warwick Medical School, University of Warwick, Coventry, UK
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decades of life and occurring more commonly in females, there are some genetic predispositions to ACC, including Li–Fraumeni, Beckwith–Wiedemann, and Lynch syndromes ( 2 ). Around 50–60% of patients with ACC present with clinical features of steroid
Department of Endocrinology, Imperial College Healthcare NHS Trust, London, UK
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Department of Endocrinology, Imperial College Healthcare NHS Trust, London, UK
Department of Clinical Biochemistry, North West London Pathology, London, UK
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Department of Endocrinology, Imperial College Healthcare NHS Trust, London, UK
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Department of Endocrinology, Imperial College Healthcare NHS Trust, London, UK
Department of Clinical Biochemistry, North West London Pathology, London, UK
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titration remains a significant clinical challenge. Serum prednisolone levels can be used to optimise doses to ensure individuals receive the minimal effective dose and avoid excess steroid exposure. Dose decreases correlate well with clinical symptomatology
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specificity ( 4 , 5 , 6 ). Cortisol analyses using liquid chromatography tandem mass spectrometry (LC-MS/MS) have eliminated the problems of cross-reactivity with exogenous steroids and cortisol metabolites often found with immunoassays ( 7 , 8 , 9 , 10
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International Centre for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
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International Centre for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
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Pediatric Endocrinology Clinic, Department of Pediatrics, Aretaeio Hospital, Nicosia, Cyprus
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International Centre for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
Department of Clinical Medicine, University of Copenhagen, Denmark
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AM & Juul A . Isotope-dilution TurboFlow-LC-MS/MS method for simultaneous quantification of ten steroid metabolites in serum . Clinica Chimica Acta 2017 468 180 – 186 . ( https://doi.org/10.1016/j.cca.2017.03.002 ) 15 Søeborg T Frederiksen
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Division of Endocrinology, Diabetes and Metabolism, Department of Medical Sciences, University of Turin, Turin, Italy
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Department of Medicine, Haukeland University Hospital, Bergen, Norway
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Department of Medicine, Division of Endocrinology, Leiden University Medical Center, Leiden, The Netherlands
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distancing, possession of a ‘steroid emergency card’ and sufficient glucocorticoid supplies including emergency preparations for oral and systemic use were advised ( 24 ). In our study, the use of emergency hydrocortisone injection was described in 2 of 64
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Department of Medicine, Monash University, Clayton, Victoria, Australia
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exogenous steroid exposure was excluded in all individuals. Adrenal vein sampling protocol AVS was performed by an interventional radiologist as a day procedure, under local anesthesia and minor sedation, and after further informed consent had been
National Institute of Endocrinology CI Parhon, Bucharest, Romania
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adrenalectomy developed AI. In contrast, only 60% of patients with cortical-sparing adrenalectomy developed AI, requiring lifelong steroid replacement (mean dose 15 mg HC/day). Similar rates of AI after CSS (43%) in patients with bilateral PHEOs have been
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intervals of 3 months and subsequently 6-monthly. Recurrence of infection (fever, anorexia and weight loss) and adequacy of steroid replacement were ascertained at each visit. Patients were encouraged to contact the treating endocrinologist for any emergency
Faculty of Biology Medicine and Health, University of Manchester, Manchester, UK
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://doi.org/10.1111/joim.12162 ) 2 Speiser PW Arlt W Auchus RJ Baskin LS Conway GS Merke DP Meyer-Bahlburg HFL Miller WL Murad MH Oberfield SE , et al. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine
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Introduction Adrenocortical carcinoma (ACC) is a rare and aggressive cancer that affects both children and adults, having an overall incidence of 1–2 cases/million per year. In most cases, cancer presents with steroid hormone excess ( 1