Searchable abstracts of presentations at key conferences in endocrinology

ea0052p34 | (1) | UKINETS2017

Grading systems in gastroenteropancreatic neuroendocrine tumours

Hobby Charlotte , Morgan Meleri , Rees Aled , Khan Mohid , Christian Adam

Objective: To compare 3 methods of generating Ki-67% in gastroenteropancreatic neuroendocrine tumours (GEP-NETs).Methods: Twenty-four slides were used to generate 49 images for analysis. Each image was analysed and 3 different methods were used to calculate Ki-67%.Results: The comparison of Ki-67% from counting and estimating using the diameter (shortcut method) was strongly positively correlated, whereas the Ki-67% from counting a...

ea0051p093 | Diabetes | BSPED2017

Transitional care pathway for diabetes at Darent Valley Hospital, Dartford

Khonji Mohamed , Khan Naveed , McEwan Kevin , Wijewarden Kishani , Gupta Alok

Introduction: Transition from paediatric to adult care is a challenging time for patients with long-term conditions (NICE, 2016), care should support patients to minimize further emotional, physical and social difficulties.Aims: To improve the quality of care for paediatric patients with diabetes through transition to adult care at Darent Valley Hospital (DVH). Our hypothesis is that is transitional care for diabetes at DVH meeting NICE guidelines or not...

ea0081ep10 | Adrenal and Cardiovascular Endocrinology | ECE2022

A case of ChAdOx1 vaccine-induced thrombocytopaenia and thrombosis syndrome leading to bilateral adrenal haemorrhage and adrenal insufficiency

Efthymiadis Agathoklis , Khan Dalia , Pavord Sue , Pal Aparna

Introduction: Vaccine-induced thrombosis and thrombocytopenia (VITT) after vaccination against SARS-CoV-2 with the adenoviral vector-based vaccines ChAdOx1 and Ad26.COV2.S has been associated with adrenal pathology, such as bilateral adrenal vein thrombosis, adrenal cortex haemorrhage and adrenal insufficiency in six percent of patients1.Case report: We report the case of a 23-year-old healthy woman who presented at eight days after ChAdOx1 va...

ea0081ep224 | Calcium and Bone | ECE2022

A pathological fracture of the femur and multiple pelvic osteolytic lesions mimicking bone metastases as the first presentation of Primary Hyperparathyroidism

Khan Haris , Nawaz Maimoona , Dang Cuong , Malik Isha

Introduction: Pathological fractures are uncommon in young patients and raise concern about malignancy. Brown tumour (osteitis fibrosa cystica) is a rare benign resorptive bone lesion reported in approximately 3% of patients with primary hyperparathyroidism (PHPT). These have become uncommon in contemporary practice and have the potential to be misdiagnosed because of radiological similarities to other bone diseases especially malignancy.We present a case where the first prese...

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...

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...

ea0082we9 | Workshop E: Disorders of the gonads | SFEEU2022

Primary female hypogonadism

Razi Ahmed Shaikh , Ali Mudassir , Devine Kerri , Iqbal Khan Irfan

Female with primary hypogonadism have inadequate function of the ovaries, with impaired production of germ cells (eggs) and sex hormones (oestrogen and progesterone). We recently came across a 22-year old female with short stature in childhood and adulthood she received growth hormone treatment (due to arrested puberty) between 3-5 years of age and further treatment at age of 10 years. She had history of IUGR, primary amenorrhoea, sensorineural deafness, congenitally missing t...

ea0082we12 | Workshop E: Disorders of the gonads | SFEEU2022

"Is there a right time to stop hormone replacement therapy?"

Iqbal Khan Irfan , Ali Rashid Razan , Razi Ahmed Shaikh

A 59-year-old woman with 46XY complete androgen insensitivity syndrome was referred back to our service. She also has history of hypertension and migraines. She was gonadectomised at the age of 15 years and treated with Ethinylestradiol. She married and was able to have enjoyable sex without the need for vaginoplasty or dilators. However, at 54 years she was firmly advised to stop Ethinylestradiol due to satisfactory bone density and “risks of HRT outweighing benefits&#14...

ea0082oc9 | Oral Communications | SFEEU2022

A case of ChAdOx1 vaccine-induced thrombocytopenia and thrombosis syndrome leading to bilateral adrenal haemorrhage and adrenal insufficiency

Efthymiadis Agathoklis , Khan Dalia , Pavord Sue , Pal Aparna

Case History: We report the case of a 23-year-old woman who developed adrenal insufficiency secondary to bilateral adrenal haemorrhage in the context of vaccine-induced thrombosis and thrombocytopenia (VITT). She presented with breathlessness and chest pain eight days after receiving her first dose of the adenoviral vector-based ChAdOx1 vaccine. Over the course of a week, she developed fulminant VITT. Her only comorbidity was obesity, with BMI of 35 kg/m2. <p class="abstex...

ea0086p307 | Adrenal and Cardiovascular | SFEBES2022

Pheochromocytoma in patient with Neurofibromatosis 1 (NF1) radiologically mimicking Neurofibroma

Tahir Chohan Muhammad , Pye So , Iqbal Khan Irfan

Introduction: NF1 or Von-Recklinghausen’s disease, an autosomal dominant neuro-cutaneous disorder results from NF1 (a tumour-suppressor gene) mutation, predisposing to neoplasms mainly affecting eye, skin and nervous system but rarely pheochromocytoma (0.1-5.7%). The incidence increases to 20-50% if NF1 is associated with hypertension.Case history: 30 years female, known NF1 since 2005 and multiple laparotomies for intra-abdominal neurofibromas pres...