Searchable abstracts of presentations at key conferences in endocrinology

ea0065p333 | Neuroendocrinology | SFEBES2019

A rare case of metastatic insulinoma

Millar Kate , Sim Sing Yang , Haider Najaf , Kar Partha

A 24 year old gentleman presented following an episode where he became ‘sleepy’ and disorientated whilst driving and had to pull over. He was confused and lethargic and paramedics found blood glucose of 2 mmol/l. He gave a 3-week history of extreme lethargy, nausea, epigastric discomfort, blurring of vision and constant hunger. He denied recent weight changes and had no significant past medical/family history. Biochemical evaluation was as follows; Laboratory glucose...

ea0062p33 | Poster Presentations | EU2019

A case of thyrotoxic periodic paralysis

Sim Sing Yee , Pierides Michael , Patel Kishor , Mani Hamidreza

Case history: Thyrotoxic periodic paralysis (TPP) which was first described in 1902 is characterised by episodes of painless muscle weakness, hypokalaemia and thyrotoxicosis without any total body potassium deficit. It predominantly affects people of Asian descent between 20 and 40 years old with a 2 percent incidence compared to 0.2 percent in non-Asian descent. The pathogenesis of TPP is related to an increase Na+/K+-ATPase activity in the skeletal muscle leading to an influ...

ea0062cb6 | Additional Cases | EU2019

Resistant Grave’s disease not amenable to Thionamides, Thyroidectomy and Radioactive iodine

Haider Najaf , Sim Sing , Butt Nouman , Cranston Iain

Grave’s disease is an auto-immune condition associated with hyperthyroidism caused by TSH-receptor antibodies (TRAB) expressed by follicular cells of the thyroid gland. Grave’s ophthalmopathy has been reported in 25% of the patients and is rarely associated with dermopathy and thyroid acropachy. Management is by anti-thyroid drugs, radioactive iodine ablation or surgery, either alone or in combination. We present a rare case of resistant Graves who has detectable ant...

ea0063gp10 | Adrenal and Neuroendocrine - Tumour | ECE2019

Brown fat proliferation- A rare complication of Phaeochromocytoma

Sim Sing Yang , Haider Najaf , Meeking Darryl , Flowers David

Phaeochromocytoma is a catecholamine producing tumour arising from the adrenomedullary chromaffin cells. It produces hormones such as epinephrine, norepinephrine, catecholamine and dopamine. (1) There have been some case reports describing an association between Brown adipose tissue (BAT) accumulation due to catecholamine excess caused by a phaeochromocytoma. We present a similar case in this abstract. A 77 year old lady was referred to the community geriatricians with symptom...

ea0070aep82 | Adrenal and Cardiovascular Endocrinology | ECE2020

Malignant collision tumour in left adrenal gland- A rare tumour

Al-Mrayat Ma’en , Sim Sing Yang

We present a 41 years old lady who presented with non specifc symptoms- lethargy, general myalgia, memory impairment. She also complained of hot flushes, sweats and had a brief episode of panic attacks hence was commence on Sertraline by the GP. She has a past medical history of appendicectomy. Her mother had lymphoma and mother died from lung cancer. She is a smoker, however is teetotal. She has 3 children and works in a laundry. She was initially referred to the haematologis...

ea0070ep10 | Adrenal and Cardiovascular Endocrinology | ECE2020

Malignant neuroblastoma mimicking a metastatic paraganglioma – case report

Maciel Joana , Teresa Alexandre Maria , Simões Helder

Background: Neuroblastomas are malignant tumors that arise from sympathetic plexus or adrenal medulla. Their clinical behavior can range from spontaneous regression to aggressive disease. Like paragangliomas, they have the capacity to secrete catecholamines and to express somatostatin receptors, which is important for diagnostic and treatment purposes. However, the differential diagnosis with paraganglioma can be challenging. We present a case of a catecholamine-producing tumo...

ea0070ep52 | Adrenal and Cardiovascular Endocrinology | ECE2020

VHL-bilateral adrenalectomy with paragangliomas (A rare entity)

Yang Sim Sing , Al-Mrayat Ma’en

Von Hippel–Lindau (VHL) disease, attributable to germline mutations in the VHL gene on the short arm of chromosome 3 (3p25-26) is an inherited condition which can give rise to paragangliomas. We present a case of 47 year old gentleman with bilateral pheochromocytomas in the past resulting in both adrenalectomies as a child in the 1980. His routine follow up subsequently picked up elevated urine Normetanephrines at 14.3 µmol/24 h 25 years postoperatively. His CT abdo...

ea0070ep267 | Endocrine-related Cancer | ECE2020

Raised Metanephrines in SDHB mutation- the hunt for the source

Yang Sim Sing , Al-Mrayat Ma’en

We present a case of a 24 year old lady with known SDHB mutation. She was referred from the genetics clinic in view of a strong family history of premature paraganglioma at the age of 17. On initial clinic assessment she exhibits no symptoms suggestive of paraganglioma or pheochromocytoma. Her blood pressure is normal at 120/75. pulse of 60–80bpm. Physical examination was unremarkable Her Plasma normetanephrine done on two separate occasion were elevated at 1600 pmol/l a...

ea0070ep436 | Thyroid | ECE2020

Coexistent thyroid and lung cancers resembling flip flop phenomenon

Cavaco Daniela , Simões-Pereira Joana , Leite Valeriano

Introduction: Differentiated thyroid cancer (DTC) prognosis is usually favorable, even when metastatic radioiodine avid disease is present. Radioiodine-refractory disease, usually a sign of higher aggressiveness, can be detected by 18F-FDG-PET/CT. There is a reverse relationship between iodine and FDG accumulation in thyroid cancer lesions, the so-called ‘‘flip-flop’’ phenomenon: when thyroid cancer cells dedifferentiate they tend to lose the...

ea0070ep576 | Hot topics (including COVID-19) | ECE2020

Challenges in hyponatremia etiology and management in a child with a suprasellar tumour

Donato Sara , Figueiredo Ana , Simões-Pereira Joana

Introduction: Hyponatremia is the most common hydroelectrolytic disturbance in clinical practice. Multiple causes exist for its occurrence, being the etiological diagnosis sometimes complex. In patients with suprasellar tumours it is even harder due to several confounding factors. Management of these patients is difficult as it conflicts with chemotherapy-associated hyperhydration protocols. We present a case that exemplifies this.Clinical case: Four yea...