Endocrine Abstracts

Contents

• Society for Endocrinology National Clinical Cases 2020
• • Oral Communications
  • • Biochemical and clinical cure of primary aldosteronism by ultrasound-guided endoscopic radiofrequency ablation

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    • Paraneoplastic hypoglycaemia secondary to IGF-2 secretion from a metastatic gastrointestinal stromal tumour

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    • A rare case of bilateral carotid body paragangliomas and associated Burkitt's lymphoma in patient with a germline SDHB mutation

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    • Come out, come out, wherever you are…….

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    • A Rare Adrenal Tumour Presenting as an Adrenal Incidentaloma

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    • MGES: Monoclonal Gammopathy of Endocrine Significance?

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    • Management challenges in a patient with papillary thyroid carcinoma and resistance to thyroid hormone

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    • Bones, Moans and Groans: A Calcium Conundrum

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    • Should SHBG be measured in every patient before diagnosing hypogonadotrophic hypogonadism?

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    • Hiding in plain sight: A case of severe refractory primary hyperparathyroidism due to an intrathyroidal ectopic parathyroid adenoma

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  • Poster Presentations
  • • Two contrasting cases of spontaneous severe hypoglycaemia secondary to anti-insulin antibodies (Insulin Autoimmune Syndrome / Hirata disease)

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    • Non-islet cell tumour hypoglycaemia in a patient with type 1 diabetes mellitus

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    • Occult ectopic ACTH: controlling the disease to find the source, with a unique sequelae

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    • Applying a novel molecular imaging technique in a case of pseudo-phaeochromocytoma

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    • Isolated ACTH-deficiency following immune checkpoint inhibitors: diagnostic challenges demonstrated by a clinical case

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    • Once pituitary adenoma is not always an adenoma

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    • Synchronous phaeochromocytoma crisis and acute anaphylaxis, precipitated by intra-articular Triamcinolone injection

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    • Management of Adipsic Cranial Diabetes Insipidus while evading methotrexate toxicity

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    • Idiopathic spontaneous bilateral adrenal haemorrhage in pregnancy

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    • A rare case of thyrotoxicosis arising as a paraneoplastic syndrome of uterine choriocarcinoma

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    • Autoimmune hypophysitis induced by Anti-PD-1 Monoclonal Antibody, Nivolumab and anticytotoxic T-lymphocyte antigen-4 (CTLA-4) agent, Ipilimumab, presenting by compressive symptoms and treated with intravenous methyl-prednisolone

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    • A case of non-islet cell tumour hypoglycaemia due to advanced hepatocellular carcinoma secondary to previously undiagnosed chronic HBV-infection

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    • Etomidate for the management of acute psychosis due to Cushing's syndrome in a patient with a glucocorticoid-secreting adrenocortical carcinoma

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    • Follow your endocrine instincts: a neurosarcoid conundrum

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    • 'Tiger Woman Sign'; Hypercalcaemia Secondary to Atypical Isolated Sarcoid Myositis

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    • Feminising adrenal tumours (FAT): the most common rare tumours of the adrenal gland?

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    • An unusual Paraneoplastic Syndromes related to Neuroendorine Tumours

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    • Don't miss the pus-an abscess of the pituitary

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    • Hypoglycaemia associated with high grade transformation of a previously non-functioning pancreatic neuroendocrine tumour (pNET)

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    • Hypercalcemia and electric storm in patient with primary hyperparathyroidism

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    • Functional heterogeneity of pancreatic neuroendocrine tumours in multiple endocrine neoplasia type 1 (MEN-1)

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    • A Grave cause of hypercalcaemia in hypoparathyroidism

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    • Myxoedema crisis: The importance of establishing cardiac baseline at admission to guide optimum thyroid function correction rate

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    • Dopamine agonists (DA) therapy down-titration may prevent CSF leakage in cases of structurally responsive macroprolactinomas

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    • GCM2 variant - A rare genetic cause of Familial Isolated Hyperparathyroidism

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    • An unusual cause of primary amenorrhoea

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    • The normalisation of a serum testosterone using GnRH analogue therapy in a case of a single testosterone-secreting adrenal adenoma confirmed on adrenal vein sampling

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    • A case of macroTSH masquerading as subclinical hypothyroidism

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    • Calcium sensing receptor mutation causing familial hypocalciuric hypercalcaemia

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    • ADHD and Addison's: similar in name, similar in nature?

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    • A rare case of carotico-cavernous sinus fistula associated with pituitary enlargement

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    • An illustrative case highlighting the risk of nephrocalcinosis with 1-alfacalcidol in chronic hypoparathyroidism

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    • Gynaecomastia as a paraneoplastic syndrome secondary to hCG secreting lung cancer

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    • Radio-iodine treatment for thyrotoxicosis in unsuspected pregnancy

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    • 'I have type 2, my brother has type 1, I can't hear you doctor! Metformin give me diarrhoea'

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    • Somatostatin analogue therapy in a patient with von Hippel-Lindau Disease and multiple pancreatic neuroendocrine tumours

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    • Liquorice: a sweet root with a sour aftertaste: A case of pseudoaldosteronism, cardiomyopathy and an upper gastrointestinal bleed

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    • Requirement of staged interventions in a complex case of Acromegaly and Obstructive Sleep Apnoea

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    • Primary hyperparathyroidism in pregnancy: Uncommon manifestation of significant weight loss

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    • The great masquerader-Phaechromocytoma presenting as ST elevation Acute Coronary Syndrome

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    • Metastatic phaeochromocytoma and catecholamine-induced cardiomyopathy

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    • Urinary retention causing severe hyponatremia, an association often missed

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    • Case report: Dramatic improvement in severely constricted visual fields within days of bromocriptine treatment in a patient with giant prolactinoma

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    • Lymphocytic Hypophysitis and Pituitary Adenoma - The diagnostic conundrum and how differentiating between the two masquerading entities forms a pivotal role in management

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    • Chronic urticaria as a rare presentation of primary hyperparathyroidism

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    • Diabetic neuropathic cachexia

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    • Fact or fiction? A discussion on the subject of Hashimoto's Encephalopathy and presentation of a case study

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    • Metabolic bone disease as presentation for primary hyperparathyroidism

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    • Amiodarone induced thyrotoxicosis presenting as significant heart failure

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    • Pregnancy against the odds

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    • Incidental diagnosis of Bilateral Adrenal Myelolipomas in a patient with Congential Adrenal Hyperplasia results in enhanced adherence to treatment, with limited evidence to guide management

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    • Hypercalcemia of advanced chronic liver disease: a forgotten clinical entity!

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    • Hyperparathyroidism and severe vitamin D deficiency: a bone breaking combination

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    • Seeing beyond a diagnosis of familial short stature

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    • 'A Case Report on Eruptive Xanthoma as the First Presentation of Undiagnosed Diabetes Mellitus'

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    • A tale of two siblings; the importance of urine calcium creatinine clearance ratio

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    • Severe symptomatic hyponatremia with SIADH picture due to influenza A

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    • Unexplained hypercortisolaemia in a patient without a Cushing's phenotype: potential for cortisol receptor mutation?

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    • Massive asymptomatic creatine kinase elevation (MACKE) as a result of aripiprazole and quetiapine use

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    • Recurrent hypoglycaemia - beyond Whipples Triad

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    • A case of pulmonary neuroendocrine tumours secreting ACTH and GHRH

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    • Breast Cancer in MEN1: Coincidence or association?

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    • Coexistence of Refetoff syndrome and papillary thyroid carcinoma

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    • So Close, Yet so Fahr!

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    • Fluctuating adrenal hyperplasia

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    • A case of sellar paraganlioma; rarest of the rare

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    • Complete recovery following osmotic demyelinating syndrome in a patient with craniopharyngioma

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    • Refractory cyclical cushing's - clinical challenges

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    • Isolated Langerhans cell histiocytosis in hypothalamic-pituitary region

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    • Insulinoma diagnosed in a patient with learning disability with presentation of seizure being treated as epilepsy for two years

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    • Metastatic clear cell renal carcinoma with initial presentation of thyroid mass

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    • Parathyroid adenoma in a young man <35 years old

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