Searchable abstracts of presentations at key conferences in endocrinology

ea0081ep532 | Diabetes, Obesity, Metabolism and Nutrition | ECE2022

A case of idiopathic postprandial syndrome in a middle-aged nigerian woman

Jesuyajolu Damilola , Mohammed Abdulhafeez , Okeke Charles , Nicholas Armstrong

Introduction: Not much has been reported about Idiopathic Postprandial syndrome, especially in Africa. Many cases are often wrongly diagnosed as reactive hypoglycemia. Idiopathic postprandial syndrome refers to signs and symptoms of hypoglycemia in the absence of low blood sugar occurring after meals and is of unknown cause. Clinical case: We report a case of Idiopathic Postprandial Syndrome in a 44-year old woman living in Nigeria. We present a 44-year-...

ea0081ep580 | Endocrine-Related Cancer | ECE2022

Solitary fibrous tumors of the pleura with Doege-Potter syndrome: a case report

Douni Sohail , Elaamadi Wafae , Sabur Safa , Bouchikh Mohammed , Abdellah Achir

Background: Solitary fibrous tumor of the pleura is a rare primary intrathoracic tumor that arises from mesenchymal tissue. Hypoglycemia associated Solitary fibrous tumor of the pleura is referred to as the Doege-Potter syndrome and is caused by inappropriate secretion of an insulin-like growth factor II.Case presentation: We report 70-year-old women with no particular medical history, who present a right chest pain for 1 year with fatigue. The clinical ...

ea0050ep041 | Clinical Biochemistry | SFEBES2017

Sertraline-induced non-hyperinsulinemic hypoglycaemia in a non-diabetic patient : A case report

Karim Rehmat , Shah Najeeb , Jadoon Nauman , Mohammed Kamrudeen

Case: A 44-year-old patient presented with symptoms of sweating, shaking and hunger, which were all eased by eating. Her symptoms were suggestive of hypoglycaemia, experienced predominantly 2-3 hours after meals. Hypoglycaemia was confirmed during these episodes. She had normal liver and renal function. There was no history of Diabetes Mellitus.Her symptoms improved slightly with measures of adjusting her diet but did not sett...

ea0050ep098 | Reproduction | SFEBES2017

Siginificant hyperandrogenism in a postmenopausal woman from a likely ovarian source

Kamath Chandan , Routledge M , Ashraf M , Premawardhana Lakdasa , Adlan Mohammed

Introduction: The polycystic ovary syndrome is the commonest cause for hyperandrogenism in young women. However, in older women, adrenal and ovarian tumours are more common, particularly if (a) hyperandrogenism is of short duration, (b) causes significant clinical androgenisation, and (c) is biochemically severe. We present an elderly woman who presented diagnostic and therapeutic challenges on account of her comorbidities.Case Present...

ea0050ep100 | Thyroid | SFEBES2017

Thymic hyperplasia in Graves’ disease – wait and see, or intervene?

Kamath Chandan , MacAleer B , Adlan Mohammed , Premawardhana Lakdasa

Introduction: There is no consensus about the management of thymic enlargement in Graves’ disease (GD). If imaging indicates ‘benign’ thymic appearances, and interval scans are stable, most authorities advocate no intervention until thyrotoxicosis is controlled. We present 3 patients with GD and incidentally found thymic enlargement.Case presentations: a. A 37-year-old female presented acutely with osmotic symptoms, a weight ...

ea0050ep041 | Clinical Biochemistry | SFEBES2017

Sertraline-induced non-hyperinsulinemic hypoglycaemia in a non-diabetic patient : A case report

Karim Rehmat , Shah Najeeb , Jadoon Nauman , Mohammed Kamrudeen

Case: A 44-year-old patient presented with symptoms of sweating, shaking and hunger, which were all eased by eating. Her symptoms were suggestive of hypoglycaemia, experienced predominantly 2-3 hours after meals. Hypoglycaemia was confirmed during these episodes. She had normal liver and renal function. There was no history of Diabetes Mellitus.Her symptoms improved slightly with measures of adjusting her diet but did not sett...

ea0050ep098 | Reproduction | SFEBES2017

Siginificant hyperandrogenism in a postmenopausal woman from a likely ovarian source

Kamath Chandan , Routledge M , Ashraf M , Premawardhana Lakdasa , Adlan Mohammed

Introduction: The polycystic ovary syndrome is the commonest cause for hyperandrogenism in young women. However, in older women, adrenal and ovarian tumours are more common, particularly if (a) hyperandrogenism is of short duration, (b) causes significant clinical androgenisation, and (c) is biochemically severe. We present an elderly woman who presented diagnostic and therapeutic challenges on account of her comorbidities.Case Present...

ea0050ep100 | Thyroid | SFEBES2017

Thymic hyperplasia in Graves’ disease – wait and see, or intervene?

Kamath Chandan , MacAleer B , Adlan Mohammed , Premawardhana Lakdasa

Introduction: There is no consensus about the management of thymic enlargement in Graves’ disease (GD). If imaging indicates ‘benign’ thymic appearances, and interval scans are stable, most authorities advocate no intervention until thyrotoxicosis is controlled. We present 3 patients with GD and incidentally found thymic enlargement.Case presentations: a. A 37-year-old female presented acutely with osmotic symptoms, a weight ...

ea0086p309 | Adrenal and Cardiovascular | SFEBES2022

Case of herbal tea causing severe hypokalaemia and hypertension

Nizami Atif , Bilal Aziz Mohammed , Hasan Ahmed Ikram , Baig Irfan

Liquorice intake is an uncommon but familiar cause of hypokalaemia and hypertension. Liquorice tea is available over the counter as herbal tea to promote general wellbeing. This case report describes a 64-year-old male patient who presented to hospital with severe hypokalaemia and hypertension. During the in-patient stay, patient was managed with potassium replacement and anti-hypertensives (avoiding medications that interfere with endocrine investigations), investigations wer...

ea0086p310 | Adrenal and Cardiovascular | SFEBES2022

Pheochromocytoma masquerading as acute coronary syndrome

Awadelkareem Abuzar , Elsaify Wael , Nag Sath , Ashwell Simon , Mohammed Azmi

Pheochromocytoma is a rare catecholamine-secreting tumor. It is potentially curable but can cause life-threatening hypertension or cardiac arrhythmias. We report a 58- years- old woman with no significant past medical history who was admitted through the emergency department with complaints of chest pain, palpitation, and nausea. She reported six months history of episodic palpitation and throbbing headaches, sometimes associated with light-headedness and dizziness. Hence, she...