Searchable abstracts of presentations at key conferences in endocrinology

ea0041ep287 | Clinical case reports - Pituitary/Adrenal | ECE2016

An adrenal vascular cyst masquerading as malignancy

Seshadri Shyam Sundar , Krishnan Singhan , Mathews Anitha , Mathews John

Introduction: Adrenal vascular cysts are rare, in most cases incidentally discovered during abdominal imaging for other reasons. We present a case of adrenal endovascular cyst with initial suspicious features of adrenal malignancy and subsequent management and complications.Case report: This 72-year-old male was initially admitted with a weight loss over 2 months and new onset fever and rigors and right leg pain. He was noted to have an abdominal mass. H...

ea0028p264 | Pituitary | SFEBES2012

Neurosarcoidosis presenting with anterior hypopituitarism and hypothalamic syndrome

Bejinariu Emanuela , Mathews Anitha

Introduction: We present a case of neurosarcoidosis presenting with anterior hypopituitarism and hypothalamic syndrome.Case Report: A 38-years old Caucasian woman presented from primary care with six-month history of secondary amenorrhoea. Additionally she reported non-specific tiredness, postural dizziness, nausea and abdominal pains. Over the same period she noticed progressive weight gain of three stones, increased somnolence, lethargy and excessive s...

ea0031p173 | Neoplasia, cancer and late effects | SFEBES2013

Insulinoma in postprandial hypoglycaemia and aggressive behaviour

Pan Shwe Zin Chit , Mathews Anitha

Background: Fasting hypoglycaemia is a common presenting symptom of insulinoma. However, insulinoma should be considered as a potential cause in those presenting with symptoms of hypoglycaemia after meal (1, 2, 3). Here we report a case who initially presented with postprandial symptoms though there was evidence of fasting hypoglycaemia subsequently.Case report: A 57-year-old lady initially presented with a 2 years history of palpitation, feeling hot, sw...

ea0050ep066 | Neuroendocrinology and Pituitary | SFEBES2017

Case report: Indolent IgG4 hypophysitis with partial anterior pituitary failure

Cheah Seong Keat , Krishnan Singhan , Mathews Anitha , Seshadri Shyam

A 79-year-old man presented with a fall and vomiting. The finding of significant postural hypotension associated with severe hypotonic hyponatraemia (Na 114 mmol/L, Osmolarity 244 mmol/L) mandated a Short Synacthen Test (cortisol 98 mmol/L at baseline and 238 mmol/L 30-minute post synacthen) and ACTH (6 ng/L) which confirmed central hypoadrenalism. This led to revelation of multiple pituitary axes involvement: hypogonadism (testosterone 1...

ea0050ep066 | Neuroendocrinology and Pituitary | SFEBES2017

Case report: Indolent IgG4 hypophysitis with partial anterior pituitary failure

Cheah Seong Keat , Krishnan Singhan , Mathews Anitha , Seshadri Shyam

A 79-year-old man presented with a fall and vomiting. The finding of significant postural hypotension associated with severe hypotonic hyponatraemia (Na 114 mmol/L, Osmolarity 244 mmol/L) mandated a Short Synacthen Test (cortisol 98 mmol/L at baseline and 238 mmol/L 30-minute post synacthen) and ACTH (6 ng/L) which confirmed central hypoadrenalism. This led to revelation of multiple pituitary axes involvement: hypogonadism (testosterone 1...

ea0059cc3 | Featured Clinical Cases | SFEBES2018

A Rare Genetic Variant of Type 1 Familial Hypocalciuric Hypercalcaemia (FHH)

Cheah Seong Keat , Khan Sidrah , Mathews Anitha , Krishnan Singhan

A 60 year old Caucasian woman was referred to endocrine clinic with persistent hypercalcaemia between 2.8 and 2.9 mmol/l (2.2–2.6), with inappropriately normal PTH at 7 pmol/l (1.48–7.63). Her hypercalcaemia was noted first in 2008. She had no signs or symptoms associated with hypercalcemia. However, she has a strong family history of hypercalcaemia, where her mother required Cinacalcet to control her hypercalcaemia despite two previous parathyroid resections. She ha...

ea0031p278 | Pituitary | SFEBES2013

Unusual presentation of acromegaly and functioning pituitary gonadotrophinoma (FSHoma)

Pan Shwe Zin Chit , Bevan-Jones Richard , Mathews Anitha

Background: Gonadotroph adenomas are the most common non-functioning pituitary adenomas in adult1, 2. However, functioning gonadotrophinomas are rare. Here, we describe an unusual presentation of concurrent acromegaly and functioning FSHoma (FSH-secreting pituitary adenoma).A 39-year-old man presented with a vague visual disturbance to the optometrist and a bitemporal hemianopia was detected.Further questioning elicited ...

ea0050ep073 | Neuroendocrinology and Pituitary | SFEBES2017

Distracting spontaneous refractory hypoglycaemia

Cheah Seong Keat , Rajan Roby , Mathews Abraham , Grant John , Krishnan Singhan , Mathews Anitha , Seshadri Shyam

Case: A 79 years old frail lady with history of dementia and hypertension presented with refractory hypoglycaemia over a period of 3 months requiring multiple admissions. During her most recent admission, she required continuous dextrose infusion to maintain euglycaemia. The severe spontaneous hypoglycaemia in this non-diabetic lady, warranted a series of investigations. TFT and Short Synacthen Test excluded thyroid dysfunction and hypoad...

ea0050ep073 | Neuroendocrinology and Pituitary | SFEBES2017

Distracting spontaneous refractory hypoglycaemia

Cheah Seong Keat , Rajan Roby , Mathews Abraham , Grant John , Krishnan Singhan , Mathews Anitha , Seshadri Shyam

Case: A 79 years old frail lady with history of dementia and hypertension presented with refractory hypoglycaemia over a period of 3 months requiring multiple admissions. During her most recent admission, she required continuous dextrose infusion to maintain euglycaemia. The severe spontaneous hypoglycaemia in this non-diabetic lady, warranted a series of investigations. TFT and Short Synacthen Test excluded thyroid dysfunction and hypoad...

ea0059ep95 | Reproduction | SFEBES2018

Localisation Challenges in Postmenopausal Hyperandrogenism

Cheah Seong Keat , Miremadi Ahmad , Khan Sidrah , Mathews Anitha , Krishnan Singhan

A 48 years old lady with BMI of 46kg/m2 was postmenopausal since age 45. Due to abdominal discomfort she had an abdominal CT, which incidentally identified bilateral adrenal adenoma (9 mm on right, 18 mm on left, with fat content). This resulted in Endocrinology referral and a history of gradually worsening hirsuitism was uncovered. Her hyperandrogenism was confirmed biochemically with markedly elevated testosterone at 6.5 nmol/l (0.0–1.8), leading to a search ...