Searchable abstracts of presentations at key conferences in endocrinology

ea0099ep374 | Endocrine-Related Cancer | ECE2024

Refractory hypokalaemia secondary to an aggressive adrenal cortical carcinoma – a case report

Choo Charlotte

Adrenal cortical carcinoma (ACC) is notorious for its aggressiveness and poor prognosis. A 71-year-old woman was found to be hypokalaemic with a serum potassium of 2.6 mmol/l [reference 3.6-5.0 mmol/l] on routine blood screening. Previous serum potassium readings were normal. She was asymptomatic and reported no gastro-intestinal losses. Her medical history was significant for hypertension, hyperlipidemia and hypothyroidism following total thyroidectomy for GravesÂ’ Diseas...

ea0099ep421 | Calcium and Bone | ECE2024

Tumour-induced osteomalacia secondary to a toe mesenchymal tumour – a case report

Choo Charlotte , Sachdev Nikhel

Tumour-Induced Osteomalacia (TIO) is a rare paraneoplastic syndrome that is often underdiagnosed given its non-specific manifestations. A 64-year-old Chinese male presented with chest discomfort and generalized weakness. He was treated for symptomatic iron deficiency anaemia, with two units of blood transfusion given his low haemoglobin of 6.1 g/dl; no intravenous iron replacement was given. Concurrently, laboratory results revealed a low phosphate level of 0.4 mmol/l [referen...

ea0099ep1010 | Endocrine-Related Cancer | ECE2024

Ectopic adrenocorticotropic hormone secretion secondary to recurrent olfactory neuroblastoma – a case report

Sachdev Nikhel , Choo Charlotte

Background: Severe hypercortisolism from ectopic adrenocorticotropic (ACTH) secretion may be life-threatening. The lung is the most common site of ACTH secreting tumours, ranging from bronchial carcinoids to small cell lung carcinoma. Olfactory neuroblastomas (ONB) are rare malignant neuroectodermal tumours. They show neuroendocrine differentiation and may exhibit a wide variety of paraneoplastic syndromes including ectopic ACTH secretion (EAS). We report a case of EAS from a ...