Searchable abstracts of presentations at key conferences in endocrinology

ea0050p023 | Adrenal and Steroids | SFEBES2017

Quality of life in patients with adrenal disease: a systematic review

Ho Winnie , Druce Maralyn

Evaluating patients with adrenal disease is uniquely challenging as biochemical parameters for assessing disease control or adequacy of hormone replacement are imprecise or lacking. QOL measures are increasingly being used to assess patients with adrenal disease, using a range of generic and disease specific measures. Reduced quality of life has been observed in patients with adrenal disease, even when biochemical cure is possible. We performed a sys...

ea0050p023 | Adrenal and Steroids | SFEBES2017

Quality of life in patients with adrenal disease: a systematic review

Ho Winnie , Druce Maralyn

Evaluating patients with adrenal disease is uniquely challenging as biochemical parameters for assessing disease control or adequacy of hormone replacement are imprecise or lacking. QOL measures are increasingly being used to assess patients with adrenal disease, using a range of generic and disease specific measures. Reduced quality of life has been observed in patients with adrenal disease, even when biochemical cure is possible. We performed a sys...

ea0050cc02 | Featured Clinical Cases | SFEBES2017

A case of giant prolactinoma with JAK 2 positive mutation

Ho Winnie , Tufton Nicola , Druce Maralyn

We present the case of a 19-year old male who presented with a generalized tonic clonic seizure associated with visual loss. Examination revealed severe visual field defects and arrested pubertal development. Laboratory evaluation revealed a very elevated prolactin of 298 410 mU/l, hypogonadotrophic hypogonadism, secondary adrenal insufficiency, and secondary hypothyroidism. He was also found to have thrombocytosis due to JAK 2 essential thrombocythaemia. Pituitary MRI reveale...

ea0050cc02 | Featured Clinical Cases | SFEBES2017

A case of giant prolactinoma with JAK 2 positive mutation

Ho Winnie , Tufton Nicola , Druce Maralyn

We present the case of a 19-year old male who presented with a generalized tonic clonic seizure associated with visual loss. Examination revealed severe visual field defects and arrested pubertal development. Laboratory evaluation revealed a very elevated prolactin of 298 410 mU/l, hypogonadotrophic hypogonadism, secondary adrenal insufficiency, and secondary hypothyroidism. He was also found to have thrombocytosis due to JAK 2 essential thrombocythaemia. Pituitary MRI reveale...