Searchable abstracts of presentations at key conferences in endocrinology

ea0055p05 | Poster Presentations | SFEEU2018

Curious case of hypercalcemia in pregnancy

Pillai Sanesh , MaCinerney Ruth

Hypercalcaemia during pregnancy is unusual and primary hyperparathyroidism is the commonest cause: we present a more unusual case.Case history: 29-year woman, 34 weeks pregnant, was admitted with hypertension and oedema. She had gestational diabetes managed with diet alone. Initial calcium level was normal; it gradually increased in the next few days though this was not noted. She was diagnosed with preeclampsia and treated with steroids for foetal lung ...

ea0028p83 | Clinical practice/governance and case reports | SFEBES2012

When is a thyroid eye not a thyroid eye?

Greig Marni , Macinerney Ruth

A 63 year old female was referred to ophthalmology in December 2007 with a 10 day history of redness, itching and watering of her left eye: the eye had congestion, chemosis and mild proptosis, and ocular movements were mildly restricted. There was no reduction in visual acuity. MRI in January reported no intraocular or intraorbital lesion, and an inflammatory cause was sought - possibly thyroid eye disease. She did not improve on pressure lowering treatments but had some impro...

ea0065p300 | Neuroendocrinology | SFEBES2019

Oxaliplatin/raltitrexed-associated nephrogenic diabetes insipidus − a new finding

Goonoo Mohummad Shaan , Dewdney Alice , MacInerney Ruth

Background: Nephrogenic diabetes insipidus (DI) is characterized by polyuria with dilute urine due to the inability of the principal cells of the renal collecting ducts to respond to antidiuretic hormone and concentrate urine. It can be drug-induced and several chemotherapeutic agents, including the platinum derivative cisplatin and the antimetabolite pemetrexed, have been reported to cause nephrogenic DI, presumably via tubular damage.Case presentation:...

ea0028p72 | Clinical practice/governance and case reports | SFEBES2012

We should “ruddy well follow them up” - An unusual complication of suboptimally treated Congenital Adrenal Hyperplasia

Shillo Pallai Rappai , Macinerney Ruth , Robinson Robert

A 40 year old man with CAH and significant needle phobia presented with left leg pain in January 2011. He had been discharged from follow up at another trust. Medications were hydrocortisone 10 mg BD and fludrocortisone 100 mcg OD. Admission haemoglobin was 19.9 g/dl, haematocrit 0.554. A thorough work up to investigate causes of polycythaemia revealed the only significant abnormality as a testosterone of 45.7 nmol/L (8–27), with low gonadotrophins. The blood sample for 1...

ea0025p104 | Clinical biochemistry | SFEBES2011

Unwanted recovery from secondary hypogonadism: paradoxical effect of Zoladex

Muniyappa Suresha , MacInerney Ruth , Robinson Rob

We present the case of an 80-year-old man found to have a non-functioning pituitary macroadenoma causing secondary adrenal insufficiency and hypogonadism in 2006. Thyroid function and prolactin levels were normal. With hydrocortisone replacement he was doing well. There was no visual field defect and he continued with conservative management. On enquiring about testosterone treatment, it had been started in Oct 2008, but discontinued within a month as there was no change in hi...

ea0074ncc21 | Highlighted Cases | SFENCC2021

Steroid responsive encephalopathy associated with autoimmune graves thyroid disease, a rare presentation

Uchambally Manjima , Nahar Meheroon , Macinerney Ruth

Case History: We describe a case of a 30-year-old female who presented at 8 weeks postpartum with history of altered behaviour, clouding of consciousness and status epilepticus. She had been diagnosed with autoimmune graves thyroid disease and was commenced on carbimazole prior to this episode. She was treated as meningoencephalitis. Also, consideration was given for possibility of thyroid storm and post-partum eclampsia. She was intubated and ventilated, treated with IV acycl...

ea0094p95 | Neuroendocrinology and Pituitary | SFEBES2023

Pituitary apoplexy with a twist

Elamin Aisha , Pallai Shillo , Macinerney Ruth , Khalifa Mai , Went Richard

Introduction: Multiple myeloma (MM) is a haematological disorder characterised by an aberrant rise in monoclonal paraprotein. Intrasellar plasmacytomas can be infrequent MM manifestations. They are challenging to diagnose and frequently mimic pituitary adenomas; however rarely present with pituitary apoplexy. We describe a patient with pituitary apoplexy-like symptoms, subsequently diagnosed with MM, whose intrasellar mass entirely resolved after chemotherapy....

ea0091cb44 | Additional Cases | SFEEU2023

Severe Cushing’s Syndrome in a 24 year old female

Sloan Gordon , Macinerney Ruth , Pillai Anita , Robinson Robert , Pallai Shillo , Shahbuddin Ibrahim

A 24 year old female presented to her general practitioner with general malaise. She had a genetic diagnosis of hereditary non-polyposis colorectal cancer (Lynch syndrome), with no colonic lesions detected on screening. Routine biochemistry revealed a potassium of 2.1mmol/l, requiring admission for urgent investigation and intravenous replacement. Further clinical assessment found a past history of severe acute thoracic back pain (3-months prior to presentation), weight gain a...

ea0038p121 | Clinical practice/governance and case reports | SFEBES2015

A case of morning headache: Doege–Potter syndrome

Kassim Saifuddin , Pillai Anita , MacInerney Ruth , Vanheeswijk Isabelle , Harsimar Jhittay , Robinson Emma

Tumour induced hypoglycaemia is a rare disorder occurring in cancer patients caused by variety of tumours including islet and non-islet tumours. Non-islet cell tumour induced hypoglycaemia (NICTH) is rare paraneoplastic disorders normally associated with pleural solitary fibrous tumour but can also rarely occur in extra thoracic site.We describe an 86-year-old man not known to have diabetes mellitus who presented with 3-month history of early morning hea...