Searchable abstracts of presentations at key conferences in endocrinology

ea0077p220 | Neuroendocrinology and Pituitary | SFEBES2021

Multiple Cell Line Pituitary Adenoma associated with PIT-1 and TPIT lineage cells resulting in acromegaly with ACTH dependent Cushing’s: a case report

Joshi Hareesh , Ye Kyaw , Bridges Leslie , Martin Andrew , Bano Gul

Introduction: Anterior pituitary cells are characterised by functional lineages based on the expression pattern of transcription factors. Functional differentiation in the form of pituitary adenomas co-secreting ACTH and growth hormone is very rare. We report a case of multiple cell line pituitary adenoma resulting in acromegaly and ACTH dependent Cushing’s.Case: A 52-year-old woman of Ghanian origin (BMI of 57.5 kg/m2) presented with pro...

ea0077lb27 | Late Breaking | SFEBES2021

Efficacy of oestrogen implant in transwomen as hormone replacement therapy

Joshi Hareesh , Gezer Emre , Espina Maricel , Seal Leighton

Background: Hormone therapy is an important part of transition for many gender nonconforming people and implant treatment is an alternative route of oestrogen administration. We assessed the efficacy of oestrogen implant in transwomen for hormone replacement therapy.Methods: 83 transgender women had 100 mg estradiol implant inserted subcutaneously in the anterior abdominal wall. All subjects graded their energy, drive and libido from a scale of 0 to 10 p...

ea0065p55 | Adrenal and Cardiovascular | SFEBES2019

Unexplained adrenal insufficiency after gastric bypass surgery

Baskaralingam Nishani , Hikmat Mondy , Joshi Hareesh , Rajkanna Jeyanthy , Oyibo Samson O , Sagi Satyanarayana V

Introduction: Gastric bypass surgery is performed for intractable severe reflux oesophagitis not amenable to vagotomy and pyloroplasty. Long-term complications include dumping syndrome, nutritional deficiencies, incisional hernia and weight loss. We report a case of unexplained adrenal insufficiency in a patient who had gastric bypass surgery.Case: A 77-year-old gentleman presented with a history of recurrent hypoglycaemic episodes. Hypoglycaemic symptom...

ea0065p127 | Bone and calcium | SFEBES2019

Severe hypercalcaemia and acute kidney Injury in a patient with sarcoidosis

Whiles Emily , Joshi Hareesh , Perumalthiagarajan Arun P , Mohammed Amina , Oyibo Samson O , Sagi Satyanarayana V

Introduction: Sarcoidosis is a multisystem granulomatous disorder. It commonly causes mild hypercalcemia in up to 10–20% of the cases and renal involvement can be a feature. Presentation with severe symptomatic hypercalcaemia (>3.5 mmol/l) and acute kidney injury is rare. We present an interesting case.Case: A 58 year old female was referred to the emergency department by her general practitioner with a one month history of polyuria, generalised wea...

ea0065p269 | Metabolism and Obesity | SFEBES2019

Severe symptomatic hyponatraemia following a minor surgical procedure

Nawaz Zahrah , Joshi Hareesh , Mehmood Taiyyab , Ukpabi Oyidiya , Oyibo Samson O , Sagi Satyanarayana V

Introduction: Hyponatraemia following surgery is usually due to a mismatch between fluid input and output peri- and post-operatively. Syndrome of inappropriate antidiuretic hormone secretion (SIADH) is another important cause of hyponatraemia, commonest cause being medications, and intrathoracic and intracranial infections and neoplasia. SIADH has been reported to occur after pituitary surgery but rarely after other types of surgery. We present a severe case of SIADH-related h...

ea0065p359 | Reproductive Endocrinology and Biology | SFEBES2019

Normosmic idiopathic hypogonadotrophic hypogonadism in two homozygous siblings with a familial novel GnRH1 gene mutation

Joshi Hareesh , Whiles Emily , Puthi Vijith , Oyibo Samson O , Sagi Satyanarayana V

Introduction: Idiopathic hypogonadotrophic hypogonadism (IHH) with normal sense of smell is a complex and rare disease entity characterised by insufficient gonadotropin releasing hormone (GnRH) neuronal action on an intact hypothalamo–pituitary–gonadal axis. IHH has an incidence of 1–10 in 100 000 live births with a variable mode of inheritance and five-fold male predominance. Gene mutations have been discovered of which 10–40% of the familial cases are due...