Searchable abstracts of presentations at key conferences in endocrinology

ea0099ep978 | Adrenal and Cardiovascular Endocrinology | ECE2024

A middle aged man presented with hypertension and adrenal incidentaloma diagnosed with pheochromocytoma

Salah Uddin Mohammad , Abourawi Fathi

Pheochromocytomas are rare tumors located in the adrenal medulla, that derive from the chromaffin cells and produce catecholamines. They are an uncommon cause of hypertension, and only 50% of the patients present symptoms compatible with this pathology. Here we describe the case of a 67-year-old man who was referred with h/o mild headache, hypertension and adrenal incidentaloma detected by CT abdomen and pelvis which showed 4.5 cm indeterminate nodule in the left adrenal gland...

ea0091wa9 | Workshop A: Disorders of the hypothalamus and pituitary | SFEEU2023

First presentation of a prolactinoma with Pituitary Apoplexy

Salah Uddin Mohammad , Deshmukh Harshal , Kabir Afrin

Pituitary apoplexy is a rare but potentially life-threatening condition that occurs due to sudden hemorrhage or infarction in a pre-existing pituitary adenoma. Here, we present a case study of a 20-year-old girl who presented to the emergency department (ED) with severe headache due to pituitary apoplexy. The patient had a history of one-year intermittent headache, which was diagnosed as migraine/cluster headache in previous ED visits. She was on Mirena coil and had amenorrhea...

ea0094p253 | Neuroendocrinology and Pituitary | SFEBES2023

Young male presented with primary hyperparathyroidism secondary to Multiple Endocrine Neoplasia type 1 syndrome

Salah Uddin Mohammad , Mohammed Kamrudeen , Deshmukh Harshal , Taqi Muhammad , Akbar Shahzad

MEN1 is a rare hereditary tumor syndrome characterized by a predisposition to a multitude of endocrine neoplasms primarily of parathyroid, enteropancreatic, and anterior pituitary origin and non endocrine tumor. Here we will discuss a case of 36 yrs. old male who was referred for high calcium on routine blood test. Subsequent investigations confirmed primary hyperparathyroidism. His serum calcium level was 2.71, PTH 7.5 Pmol/l, and vitamin D 57.4 nmol/l on presentation and was...