Endocrine Abstracts

Introduction: The non-insulinoma pancreatogenous hypoglycemia syndrome (NIPHS) identifies a group of hyperinsulinemic hypoglycemic patients with unique clinical, diagnostic, surgical, and pathologic features. A selective arterial calcium stimulation test (SACST) with hepatic venous sampling can be performed to distinguish between a focal abnormality (insulinoma) and a diffuse process (islet-cell hypertrophy/nesidioblastosis). In patients with insulinoma, the response is positi...

Introduction: The most frequently secreted hormone in pituitary adenomas is prolactin, but prolactin and growth hormone co-secretion are also seen at not an uncommon frequency. Co-secretion of growth hormone has also been reported after long-term follow up in the prolactinoma patients which well controlled with cabergoline therapy. In this case report, we aimed to discuss the results of cabergoline therapy in a case of co-secreting GH and prolactine with a normal IGF1 level an...

Introduction: Pheochromocytomas are rare catecolamin-secreting neoplasms. The classic triad of symptoms in patients with a pheochromocytoma consists of episodic headache, sweating and tachycardia. Gastrointestinal spectrums have been reported such as chronic constipation, intestinal pseudo-obstruction or even intestinal perforation. We describe patient who presented with non-mechanical bowel obstruction and interestingly hydronephrosis and acute kidney injury as a consequence ...

Introduction: High thyroid hormone levels with unsupressed TSH (atypical hyperthyroxinemia) is one of the difficult endocrinologic conditions. When the conditions leading to euthyroid hyperthyoxinism are excluded, TSH secreting pituitary adenomas (TSHoma) and thyroid hormone resistance beta syndrome (THRB) lead to this picture as rare diseases. This report aims to evaluate the diagnostic and therapeutic stages in the case of TSH-secreting pituitary microadenoma which response ...