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Adrenal News
Flushing, diaphoresis and palpitations in a woman with a retroperitoneal mass
A 34-year-old woman was referred for a four-year history of episodic hypertension, palpitations, flushing and diaphoresis.
LRP5 polymorphisms may be associated with increased bone mass in prepubertal children with premature adrenarche
Prepubertal children with premature adrenarche had higher bone mineral density when compared with healthy children in a new cross-sectional study. However, bone size-adjusted BMD or height-adjusted BMD was not significantly different between the two groups.
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Glucocorticoid treatment additionally affected bone mass in women treated for Cushing’s syndrome
Researchers have identified an additional deleterious effect of glucocorticoid therapy in women treated for Cushing’s syndrome.
Anti-21-hydroxylase antibodies, HLA class II predicted Addison’s disease
New observational Norwegian registry data reveal that Addisons disease is almost exclusively autoimmune, and is associated with high autoimmune comorbidity.
Subclinical hypercortisolism was associated with low BMD
Researchers have discovered a high prevalence of vertebral fractures and low bone mineral density among eugonadal men with adrenal incidentalomas.
Androstenediol predicted diaphyseal bone strength during late puberty
Late-pubertal diaphyseal bone mass, modeling and strength were predicted by renal excretion levels of androstenediol that were collected from healthy adolescents two years before puberty onset.
Hypertension, hypokalemia and a slightly enlarged left adrenal gland
A 35-year-old obese black woman with hypertension resistant to triple antihypertensive therapy including lisinopril 40 mg daily, atenolol 100 mg twice daily and hydrochlorothiazide 25 mg daily was referred to the endocrine clinic for the evaluation of an endocrine cause of hypertension.
Who should be tested for Cushing’s syndrome and what is the best testing method?
Screening should be based on clinical judgment.
The difficulties of Cushing’s syndrome
For as long as it has been described, Cushing’s syndrome has presented physicians with a problem. Harvey Cushing first described it in 1932, and the diagnosis, differential diagnosis and treatment of Cushing’s have remained a major challenge for endocrinologists ever since.
Pheochromocytoma imaging with an unremarkable biochemical evaluation
Patient is a 65-year-old white man with a past medical history significant for severe coronary artery disease, arrhythmias, hypertension, hyperlipidemia, anxiety and type 2 diabetes. He was referred to the endocrine clinic for the evaluation of a right adrenal nodule. The adrenal mass was found incidentally on an abdominal CT performed as part of an evaluation for epigastric pain caused by peptic ulcer disease.
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Headline News
‘Truly alarming’: Life expectancy gap in the US now up to 20 years
November 22, 20243 min read -
Headline News
Autoantibodies present in long COVID, but not a ‘smoking gun’ for new autoimmune disease
November 25, 20242 min read -
Headline News
Cardiovascular disease deaths rising among younger adults living in rural areas
November 15, 20243 min read