Searchable abstracts of presentations at key conferences in endocrinology

ea0099p330 | Pituitary and Neuroendocrinology | ECE2024

A case of type 2 diabetes masked by insulinoma

Li Adrian , Khalilova Samira

Introduction: Insulinomas are the most common functioning endocrine neoplasms of the pancreas. 53% of patients are diagnosed within five years of experiencing their first symptoms. Surgical resection is the primary treatment modality. However, patients awaiting surgery or who are not surgical candidates have achieved symptomatic relief from medical therapy. Cases of insulinoma masking diabetes has been described but are rare and diabetes often presents following surgery. Here,...

ea0099p544 | Pituitary and Neuroendocrinology | ECE2024

A case of sporadic metastatic medullary cancer with distant metastases and negative RET mutation

Khalilova Samira , Li Adrian

Introduction: Medullary thyroid cancer accounts only 1% to 4% of thyroid cancer cases (1). 25% of cases are familial secondary to germline RET mutation, while the remaining 75% are sporadic and also harbour a somatic RET mutation in more than half of all cases. Up to 15–20% of patients will present with distant metastatic disease. The standard treatment for MTC is total thyroidectomy and dissection of cervical lymph node compartments. Post-operative levels of serum calcit...

ea00100wh2.2 | Workshop H: Miscellaneous endocrine and metabolic disorders | SFEEU2024

A case of type 2 diabetes masked by insulinoma

Khalilova Samira , Li Adrian

Introduction: Insulinomas are the most common functioning endocrine neoplasms of the pancreas. 53% of patients are diagnosed within five years of experiencing their first symptoms. Surgical resection is the primary treatment modality. However, patients awaiting surgery or who are not surgical candidates have achieved symptomatic relief from medical therapy. Cases of insulinoma masking diabetes has been described but are rare and diabetes often presents following surgery. Here,...

ea0062wc3 | Workshop C: Disorders of the thyroid gland | EU2019

When TFTs just don’t add up

Li Adrian , Saqib Aaisha , Carroll Paul

A 31-year-old man originally from Ukraine attended the clinic having been started on Carbimazole 20 mg by his GP. His symptoms included intermittent palpitations, sweating and poor sleep and they had improved since starting anti-thyroid therapy. He was originally diagnosed with thyrotoxicosis in Germany in 1999 but was not treated and he re-presented in 2005. This time he was started on Carbimazole but stopped treatment on his own accord after a month because his symptoms impr...

ea0062wc9 | Workshop C: Disorders of the thyroid gland | EU2019

When thyroid function tests remain deranged despite treatment

Saqib Aaisha , Li Adrian , Carroll Paul

A 60 year old lady was diagnosed with thyrotoxicosis in 1985 (aged 28) five months postpartum. She underwent partial thyroidectomy in 1990 (age 32). Thyroid tests remained abnormal and in 1992, she underwent radio-iodine treatment requiring post-treatment. She remained under endocrine supervision and the TSH was found to be persistently elevated with normal free thyroid hormone levels (whilst on Levothyroxine). Issue with compliance and assay interference were considered. She ...

ea0074ncc13 | Highlighted Cases | SFENCC2021

Refractory Graves’ disease following total thyroidectomy caused by concurrent ectopic thyroid tissue in the anterior mediastinum

Sathyanarayan Sheela , Li Adrian , Arshad Sobia , Dimitriadis Georgios K

Case History :A 34-year-old Caucasian female patient presented in May 2015 to A&E with symptoms of overt thyroid dysfunction. She was managed medically until June 2016 when thionamide treatment was withdrawn. Unfortunately, this lady had a first disease relapse in July 2018 whilst she was pregnant at 35 weeks of gestation and then further disease relapse in January 2020 during her second pregnancy. Investigations: Initial biochemistry in 2015 confirm...

ea0074ncc14 | Highlighted Cases | SFENCC2021

Multiple electrolyte disturbances as the presenting feature of MEN-1

Li Adrian , Sathyanarayan Sheela , Arshad Sobia , Aylwin Simon , Dimitriadis Georgios

Case history: A 49-year-old teacher presented to his GP with lethargy and lower limb weakness. He had noticed polydipsia and polyuria, and had experienced weight loss albeit with an increase in central abdominal fat mass. He had previously undergone cholecystectomy and colonic polypectomy. He took no regular medications. Investigations: He had hypercalcaemia 3.34 mmol/l with PTH of 356 ng/l and hypokalaemia 2.7 mmol/l and was admitted for intravenous flu...

ea0055p18 | Poster Presentations | SFEEU2018

Type 1 diabetes presenting with unilateral left foot drop

Li Adrian P Z , Best Jonathan , Kariyawasam Dulmini , Brackenridge Anna , Thomas Stephen , Maltese Giuseppe

Case history: A 26-year-old lady presented with a two-week history of weakness associated with pins and needles affecting the lateral calf and dorsomedial aspect of her left foot. The patient denied any trauma or symptoms including weight loss. She had no drug allergies and was taking no regular medications. She had a vegan diet supplemented with multivitamins. Her past medical and family history was unremarkable. On examination, she had a narrow-based high-steppage-gait. Lowe...

ea0062wb1 | Workshop B: Disorders of growth and development | EU2019

Ectopic posterior pituitary syndrome with hypopituitarism and pubertal delay

Howells Lara , Saqib Aaisha , Bakhit Mohamed , Li Adrian , Joshi Mamta , Carroll Paul

A 19 year old Bangladeshi male attended ED with a fractured finger. He was noted to have a severely delayed bone age of 13.5 years, and no facial hair. He had moved to the UK aged 11 and could recall little information regarding his childhood or his parents. He had no significant medical co-morbidities, and in particular no history of mumps, measles or testicular injury. He reported being the shortest in his class, and being unable to keep up with his classmates in physical ac...

ea0050p285 | Neuroendocrinology and Pituitary | SFEBES2017

Prevalence of paraganglioma at first screen in SDH mutation carriers identified through family screening

Mohamed Isra Ahmed , Velusamy Anand , Izatt Louise , Li Adrian , Joshi Mamta , Breen Louise , McGowan Barbara , Powrie Jake , Obholzer Rupert , Carroll Paul V

Introduction: Mutations in the succinate dehydrogenase gene (SDH) predispose to the development of paraganglioma (PGL) which arise from parasympathetic and extra-adrenal sympathetic-associated chromaffin tissues. Identification of an index case results in family ‘cascade’ screening, often of asymptomatic individuals.Aims: To identify prevalence of PGL tumours and elevated plasma metanephrines at first scre...