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Endocrine Abstracts (2015) 37 EP700 | DOI: 10.1530/endoabs.37.EP700

11st Medical Propedeutic Department of Internal Medicine, AHEPA University Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece; 2Department of Endocrinoloy, Metabolism and Diabetes, Aretaeio Hospital, School of Medicine, University of Athens, Athens, Greece.


Introduction: Cushing’s syndrome is a rare (0.004%) hormonal disorder, which develops due to hypercortisolaemia. Cushing’s disease refers to a corticothroph cell pituitary tumour overproducing ACTH, which induces abnormally increased cortisol production from the adrenal glands. Cushing’s disease is a causative factor of osteoporosis, hypertension, glucose intolerance and dyslipidaemia.

Case report: A 50-year old woman was referred to our department for the investigation of osteoporosis. She reported a 2-year history of weight gain, hypertension and hair loss and currently a fracture of her left wrist. Reported age of menopause, 49 years. On physical examination her blood pressure was 140/90, she was overweight (BMI=25) and had bilateral supraclavicular fullness, buffalo hump, calf bruises and white striae on the abdomen. Laboratory examination revealed shortened APTT, eosinopenia, increased fasting glucose, dyslipidemia, high-normal sodium levels (Na+=145 mmol/l), mild hypokalemia (K+=3.4), hypercortisolaemia (cortisol=754 nmol/l, n.v. 171–536), FSH=132 mIU/ml, LH=36.9 mIU/ml, ACTH=136 pg/ml (n.v. 0–60), PTH=10.8 (n.v. 1.58–6.03) and 24-h urinary free cortisol=436.4 μg/dl (n.v.10–110). Estimation of lumbar spine bone mineral density by dual-energy X-ray absorptiometry was diagnostic of osteoporosis (T score −3.3). The patient underwent dynamic investigation with dexamethasone-suppressed CRH stimulation (Dex-CRH) test, which indicated ACTH-dependent Cushing’s disease. 3 Tesla MRI of the pituitary gland suggested the presence of a microadenoma. Bilateral inferior petrosal sinus sampling (IPSS) established the diagnosis of a microadenoma on the right anterior part of the pituitary gland. Treatment was started with pasireotide 2×900 μg daily.

Conclusion: Mortality in Cushing’s disease is by eight-times higher than in the general population, especially when the disease is not fully controlled. Unfortunately, many disease-related complications such as hypertension, dyslipidemia and osteoporosis are not completely reversible when diagnosis is delayed. We suggest the diagnosis of Cushing’s disease to be considered in the differential diagnosis of osteoporotic fractures or osteoporosis.

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