Searchable abstracts of presentations at key conferences in endocrinology

ea0050cc08 | Featured Clinical Cases | SFEBES2017

Pseudohypervitaminosis D due to assay interference

Khan Muhammad Ilyas , Ali Shah Syed Saad , Chikthimmah Vineeth

Assay interference with various laboratory measurements has been reported in the presence of paraproteins. We report a case of a 57 year old woman, who was referred to endocrine clinic after being found to have elevated total vitamin D levels of 369 and 336 nmol/l (normal 50–100 nmol/l). She was not known to be on any Vitamin D supplements that could account for such high levels. Around the time of referral, she was also diagnosed with IgM paraproteinaemia. Therefore, pos...

ea0086p340 | Metabolism, Obesity and Diabetes | SFEBES2022

"Severe Lipaemia" with triglyceride levels above 100 mmol/L: successfully treated with insulin therapy alone

Tahir Chohan Muhammad , Aboushareb Fathy , Shah Ahmad , Jones Susan

Introduction: Commonest causes of pancreatitis are alcohol and gallstones but less common causes like hypertriglyceridemia should also be considered as management may differ.Case history: 47 years old gentleman with history of pancreatitis and hyperlipidaemia type1 taking atorvastatin and bezafibrate, admitted with severe abdominal pain and vomiting. He was non-smoker and non-drinker. No history of cholelithiasis or medications causing pancreatitis. He w...

ea0086p368 | Thyroid | SFEBES2022

Falsely elevated serum TSH in a mother and her four children

Darrat Milad , Shah Shilpa , Halsall David , Schoenmakers Nadia , Bradley Una

Background: Elevated TSH concentration should be assessed and treated with caution because of the possibility of transient thyroid dysfunction, or, in rare cases, measurement interference. We describe a case with a rare cause of elevated TSH level in a 39-year-old mother and her four children.Case Summary: A 39-year-old lady was referred with a long history of high serum TSH ranging between 18.9 to 38.7 (reference interval 0.4-4.0 mU/l) with FT4 concentr...

ea0090p344 | Diabetes, Obesity, Metabolism and Nutrition | ECE2023

Changes in Glycemic Risk Index (GRI) and its Association with other Continuous Glucose Monitoring (CGM) Metrics after Automated Insulin Delivery System Initiation in Adults with Type 1 Diabetes

Akturk Halis , Karakus Kagan , Klonoff David , Shah Viral

Objective: To evaluate the GRI and its association with other CGM metrics after initiation of automated insulin delivery (AID) system in adults with type 1 diabetes (awT1D).Methods: Up to 90 days of CGM data before and after initiation of an AID system from 185 awT1D were collected. GRI with hypoglycemia and hyperglycemia components and other CGM metrics were calculated using cgmanalysis R software and analyzed for 24-hour, nighttime, and daytime. GRI va...

ea0090p162 | Pituitary and Neuroendocrinology | ECE2023

An unusual sellar dermoid cyst

Akbar Shahzad , Taqi Muhammad , Shah Najeeb , Mongolu Shiva , Aye Mo

Introduction: Dermoid cysts are rare (0.5% of intracranial tumours). They are best considered a spectrum: from epidermoid cysts containing desquamated squamous epithelium to teratomas containing all three embryonic tissues. Sellar dermoid cysts are even rarer [Orpha.net ID: ORPHA:91351]. Case: A 47-year old white British male was referred following incidental discovery of bitemporal field defect on routine eye test. He was otherwise completely asymptomat...

ea0090ep740 | Pituitary and Neuroendocrinology | ECE2023

Pituicytoma – case report of an extremely rare and little-studied primary tumour of the adult neurohypophysis

Taqi Muhammad , Akbar Shahzad , Malik Shah Rukh , Mongolu Shiva

The pituicytomas are extremely rare and little-studied primary tumours of the adult neurohypophysis. These are low-grade (World Health Organization [WHO] grade 1), indolent gliomas which present as a sellar mass, which is usually mistaken for a pituitary adenoma, and has no known hormonal secretory function. A 63 years old retired paediatrician was referred to the neurology clinic with the history of constant severe headache ongoing for a few weeks. It involved the whole of th...

ea0069p16 | Poster Presentations | SFENCC2020

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

Deshmukh Harshal , Shah Najeeb , Sathyapalan Thozhukat , Mongolu Shiva

Case history: Adrenal masses are often a diagnostic challenge and can present with unusual symptoms. We describe a case of a 37-year-old male with a background of ulcerative colitis, who presented with bilateral gynecomastia in the breast clinic of, worsening over last one year. He had marked breast tenderness, a decline in his libido but no erectile dysfunction. There was no history of recreational drug use.Investigations: His serum biochemistry showed ...

ea0068p20 | Abstracts | UKINETS2019

A retrospective study of FDG uptake in pathologically confirmed DIPNECH and its contributing variables

Odedra Krishan , Shah Tahir , Geh Ian , Hughes Simon

Introduction: Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia (DIPNECH) is documented as a pre-malignant condition by the World Health Organisation. Patients with pulmonary nodules typically undergo 5′-18fluoro-deoxy-D-glucose (FDG) positron emission tomography combined with computed tomography (PETCT) for further diagnostic investigation. DIPENCH is widely accepted as an FDG negative pathology. The purpose of this analysis was to a...

ea0065p425 | Thyroid | SFEBES2019

Severe proximal myopathy with high creatine kinase levels secondary to Hashimoto’s thyroiditis

Shah Najeeb , Jervis William , Mongolu Shiva , Sathyapalan Thozhukat

A 30-year-old teacher with no past medical history presented with a 3 month history of muscle weakness, pain and spasms together with cold intolerance, weight gain and fatigue. She had a baby 4 months prior to this and 2 months after delivery noticed palpitations, insomnia and tiredness which resolved spontaneously. She was a non-smoker who did not consume alcohol. She was not on any medication. There was no family history of endocrinopathy. Clinical examination revealed proxi...

ea0049ep190 | Endocrine tumours and neoplasia | ECE2017

A challenging case of metastatic paraganglioma and metastatic melanoma and prolactinoma

Karim Rehmat , Mohammed Kamrudeen , Zaheer Shah Najeeb , Fahad Arshad Muhammad

Background: Paragangliomas are extremely rare endocrine tumours and can cause diagnostic difficulty, especially with a coexistent metastatic malignancy.Case: A 78-year-old man with diagnosed metastatic melanoma underwent a PET scan for staging of the malignancy. It showed a left upper quadrant mass with multiple skeletal deposits and a lesion in the pituitary all with intense focal uptake. The mass was unusual for a metastatic lesion from melanoma althou...