Searchable abstracts of presentations at key conferences in endocrinology

ea0094p92 | Neuroendocrinology and Pituitary | SFEBES2023

A functioning gonadotroph macroadenoma presenting with features of OHSS and sustained remission 4-years after TSS

Khalilova Samira , Gonzales Christine , E Drakou Eftychia , K Dimitriadis Georgios

It is well established that the majority of the immunohistochemically confirmed gonadotroph adenomas are hormonally silent, accounting almost 64% of all clinically nonfunctioning pituitary adenomas. Whereas clinically functioning gonadotroph adenomas (FGA) are very rare and the exact prevalence is not known. We present the case of a FGA in a premenopausal. A 31-year-old female presented in the ED with oligomenorrhea for 11 months, abdominal pain and distention over the precedi...

ea0094p239 | Neuroendocrinology and Pituitary | SFEBES2023

An aggressive prolactinoma with orbital involvement and excellent response to treatment with temozolamide. A case report and systematic literature review

Khalilova Samira , Gonzales Christine , E Drakou Eftychia , K Dimitriadis Georgios

A proportion of prolactinomas exhibit aggressive features (including invasiveness, relevant growth despite adequate dopamine agonist treatment, and recurrence potential) and few may exhibit metastasizing potential (carcinomas). We present an uncommon case of intra-orbital spread from a large infiltrative prolactinoma, with excellent response to temozolomide and a systematic review of the literature. A 55y.o male patient presented with generalized weakness and hyponatraemia. Fu...

ea0050ep061 | Neoplasia, Cancer and Late Effects | SFEBES2017

Hypertestosteronemia and primary infertility from a mediastinal extragonadal germ cell tumor

Dimitriadis Georgios K , Mytilinaiou Maria , Davasgaium Allan , Sambrook Diane , Drakou Eftychia E , Hewins Claire , Nalawade Nilisha , Randeva Harpal S

A 26-year-old Caucasian male presented to the joint infertility outpatients clinic with primary infertility. His medical history included hypertrophic cardiomyopathy (HCM) due to genetically confirmed MYH7 sarcomere protein mutation, treated with implantable cardioverter-defibrillator while his partner was a healthy 24-year-old Caucasian nulliparous female. Initial investigations showed hypertestosteronemia (Testosterone: >...

ea0050ep061 | Neoplasia, Cancer and Late Effects | SFEBES2017

Hypertestosteronemia and primary infertility from a mediastinal extragonadal germ cell tumor

Dimitriadis Georgios K , Mytilinaiou Maria , Davasgaium Allan , Sambrook Diane , Drakou Eftychia E , Hewins Claire , Nalawade Nilisha , Randeva Harpal S

A 26-year-old Caucasian male presented to the joint infertility outpatients clinic with primary infertility. His medical history included hypertrophic cardiomyopathy (HCM) due to genetically confirmed MYH7 sarcomere protein mutation, treated with implantable cardioverter-defibrillator while his partner was a healthy 24-year-old Caucasian nulliparous female. Initial investigations showed hypertestosteronemia (Testosterone: >...

ea0069oc2 | Oral Communications | SFENCC2020

Paraneoplastic hypoglycaemia secondary to IGF-2 secretion from a metastatic gastrointestinal stromal tumour

Onyema Michael , Drakou Eftychia , Giovos Georgios , Leca Bianca , Ganguly Ratnadeep , Murthy Narasimha , Grossman Ashley , Randeva Harpal , Dimitriadis Georgios

Case history: Herein, we report the case of a 79-year-old male who presented acutely to A&E with recurrent episodes of symptomatic hypoglycaemia. A random glucose at presentation was low at 1.4 mmol/l and upon correction symptoms resolved. While hospitalized, he continued having episodes of symptomatic hypoglycaemia, requiring treatment with intravenous dextrose and per os steroids. Once stable, he was discharged with advice.Investigations: ...