Searchable abstracts of presentations at key conferences in endocrinology

ea0091wc2 | Workshop C: Disorders of the thyroid gland | SFEEU2023

Amiodarone induced thyrotoxicosis- A challenging case to manage

Faheem Muhammad , Aziz Umaira , Malhotra Gaurav

Amiodarone is commonly prescribed anti-arrhythmic drug which can lead to thyroid dysfunction manifesting as either hypothyroidism or hyperthyroidism. This clinical case of amiodarone induced thyrotoxicosis is being reported to highlight the challenges faced during its management. A 72-year-old gentleman was admitted with history of recurrent falls. He had past medical history of non-ischemic cardiomyopathy, CRT, atrial fibrillation, vascular dementia, osteoporosis, primary hyp...

ea0091cb50 | Additional Cases | SFEEU2023

Cushing’s syndrome due to ectopic ACTH secretion

Faheem Muhammad , Malhotra Gaurav , Aziz Umaira

Ectopic ACTH is an infrequent cause of Cushing’s syndrome which can be severe in its presentation and needs immediate management to in order to prevent the complications associated with severe hypercortisolism. This case of ectopic ACTH secretion is being reported who presented clinically as Cushing’s syndrome and later diagnosed to have small cell carcinoma of lung. A 62-year-old previously normally fit and well lady presented with 1-month history of feeling unwell,...

ea00100wd3.3 | Workshop D: Disorders of the adrenal gland | SFEEU2024

Bilateral phaeochromocytoma heralding a diagnosis of MEN 2A

Faheem Muhammad , Casey Ruth , Stokes Victoria , Schoenmakres Nadia

Pheochromocytoma is a rare catecholamine producing neuroendocrine tumor arising from the adrenal medulla. Approximately 40% of cases are hereditary and the remaining are sporadic. There are several familial syndromic disorders associated with phaeochromocytoma including: von Hippel-Lindau (VHL) syndrome, multiple endocrine neoplasia type 2 (MEN2) and, neurofibromatosis type 1 (NF1). Bilateral phaeochromocytoma should prompt suspicion of a hereditary familial syndrome such as M...