Searchable abstracts of presentations at key conferences in endocrinology

ea0031p312 | Pituitary | SFEBES2013

Metformin treatment of PCOS: St George's Hospital Endocrine Unit Clinical Experience

Walton Hannah , Mason Helen , Bano Gul

Polycystic ovary syndrome (PCOS) is the most common endocrine condition affecting women and is associated with hyperinsulinaemia and hyperandrogenism. Obesity is present in at least 30% of cases and plays a vital role in the development and maintenance of PCOS as well as affecting the severity of the clinical and endocrine features. Significant improvements in symptoms of androgen excess and ovulatory function are seen with even a modest weight loss of 5% in women with PCOS. M...

ea0021p73 | Clinical practice/governance and case reports | SFEBES2009

Recurrent pituitary apoplexy

Krishnan Binu , Loh Vooi , Bano Gul

Pituitary apoplexy is uncommon and the incidence is quoted to be between 5 and 16% in pre-existing pituitary adenomas. Recurrent pituitary apoplexy is rarer; we report 2 such cases.A 22-year-old female underwent transsphenoidal resection of an expanding intrasellar lesion in 1987. She was commenced on hydrocortisone for cortisol deficiency and on subsequent follow-up, on thyroxine. She required repeated surgery in 2003 and 2005 after she presented with h...

ea0015p61 | Clinical practice/governance and case reports | SFEBES2008

Like mother like son: a case of maternal and neonatal water intoxication

Simmgen Marcus , Nussey Stephen , Bano Gul

A 37-year old woman developed grand-mal seizures shortly after having given vaginal birth at term. Three hours later, her newborn son also had a tonic-clonic seizure. Following the convulsions, maternal fractures of the humerus and the neck of femur were detected.The pregnancy had been uneventful except for hip pains for 4 weeks prior to delivery. For years, the patient had been ingesting 5 l of bottled water daily. Labour had set in spontaneously and sh...

ea0056p107 | Clinical case reports - Thyroid/Others | ECE2018

Searching for the cause of high HCG in a man

Rehman Tejhmal , Hameed Ali , Bano Gul

Beta-human chorionic gonadotropin (β-hCG) is normally produced by syncytiotrophoblasts of the placenta and may also be secreted by germ cell neoplasms. An increase of serum hCG concentration in a male patient often suggests malignant neoplasms with a trophoblastic element. Common examples include classic seminoma with syncytiotrophoblast-like giant cells, combined germ cell tumour, and choriocarcinoma. Non-gestational choriocarcinomas typically arise from gonadal...

ea0094p201 | Endocrine Cancer and Late Effects | SFEBES2023

Paraganglioma syndromes data from a single centre

Tavoukjian Vera , Bano Gul , Alsters Suzanne

Paraganglioma syndromes (PGL) encompass a diverse group of rare neuroendocrine tumours that are characterised by hereditary predisposition and present unique diagnostic and management challenges. We performed an audit to assess the prevalence, presentation, testing, diagnosis, and treatment of these patients. We did a retrospective analysis of the genetic database and medical records of PGL patients diagnosed and managed at our hospital up till April 2023. A total of 119 cases...

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...

ea0055oc1 | National Clinical Cases | SFEEU2018

Testosterone secreting clear cell ovarian tumor in a patient with Von Hippel Lindau (VHL) disease

Rehman Tejhmal , Hameed Ali , Snape Katie , Hodgson Shirley , Bano Gul

The VHL gene is a tumor suppressor gene located on chromosome 3p25.3. Mutations in this gene prevent production of the VHL protein and as a result, cells grow and divide uncontrollably to form the tumors and cysts. Germline VHL gene mutations predispose to a variety of tumors, most commonly retinal and cerebellar haemangioblastomas, renal cell carcinoma and phaeochromocytoma. Papillary cystadenomas of the epidididymis are seen in 10–26% of men are rarely...

ea0055p11 | Poster Presentations | SFEEU2018

A challenging case of rapidly enlarging thyroid mass

Rehman Tejhmal , Hameed Ali , Kim Dae , Pettengell Ruth , Bano Gul

A 60 year old Caucasian woman presented with a three month history of rapidly enlarging neck swelling and hoarseness of voice. Her past medical history included Hypothyroidism. Her neck ultrasound scans showed 3.5 cm left thyroid nodule with bilateral lymphadenopathy (U5). The Fine needle aspiration (FNA) revealed densely grouped variable sized irregular epithelial cells with nuclear atypia and spindle shaped fragments with focal areas of lymphocytic thyroiditis. The different...

ea0082p24 | Poster Presentations | SFEEU2022

A tricky situation: hypercalcaemia in pregnancy

Dhar Mili , Smout Vera , Ahamed Sadiq Shafana , Bano Gul

Section 1: Case history: A 39-year-old Asian lady at 18 weeks of gestation, after in vitro fertilisation pregnancy, was found to have an adjusted calcium level of 3.08 (range 2.20-2.60 mmol/l) on routine blood tests. She was asymptomatic. Her Parathyroid hormone (PTH) was 14.1 (1.1-6.9pmol/l) and 25 hydroxy vitamin D 16 (15-174 nmol/l). She had insulin treated diabetes following an episode of pancreatitis for which no cause was identified. She was treated as an inpati...

ea0082p26 | Poster Presentations | SFEEU2022

An unusual cardiovascular manifestation of hyperthyroidism

Smout Vera , Dhar Mili , Ahamed Sadiq Shafana , Bano Gul

Case History: 41-year-old female presented with a 3-day history of fever, cough, and breathlessness. She had palpitations, diarrhoea and weight loss of 4-5 kg over 1 month. Graves” disease had been diagnosed 5 years prior to this episode and she had been treated with carbimazole but was not in remission. On this occasion, she was febrile and had atrial fibrillation. She also had right pleural effusion and bilateral pedal oedema.Investigations: Blood...