Searchable abstracts of presentations at key conferences in endocrinology

ea0049ep1022 | Pituitary - Clinical | ECE2017

Non-functioning pituitary adenoma; improved endocrine outcomes with increasing surgical experience: The Manchester Cohort

Giritharan Sumithra , Kearney Tara , Gnanalingham Kanna

Case notes of 150 consecutive patients (58% male) who underwent pituitary surgery by a single surgeon for non-functioning pituitary adenoma and endocrine follow up at our centre between July 2005 and February 2015 were reviewed. All patients underwent endoscopic transsphenoidal surgery as the first approach. Post-operative pituitary function was assessed by measurement of baseline pituitary hormonal profile and a glucagon stimulation test to assess ACTH and GH axis. Mean age a...

ea0044p146 | Neuroendocrinology and pituitary | SFEBES2016

Low risk of GH deficiency post subarachnoid haemorrhage

Giritharan Sumithra , Gnanalingham Kanna , Kearney Tara

Introduction: Current literature suggests that the incidence of GH deficiency (GHD) post subarachnoid haemorrhage (SAH) ranges from 0 to 37%. We present the results from a large single centre study and discuss factors that should be considered when testing for GHD in this population.Method: One hundred survivors of SAH were screened with a glucagon stimulation test (GST) for pituitary hormone deficiency. Participants with isolated GHD were required to un...

ea0031p285 | Pituitary | SFEBES2013

Rapidly progressive pituitary carcinoma in a young female

Giritharan Sumithra , Kearney Tara , Gnanalingham Kanna

A 32-year-old female presented with a 6-week history of worsening headaches associated with bitemporal visual field defects. An urgent MR scan demonstrated a sizeable pituitary lesion with chiasmal compression and suprasellar extension. Endocrine tests revealed hyperprolactinaemia (2550 mU/l) with hypocortisolaemia (<37 nmol/l). Cabergoline and hydrocortisone replacement were initiated. Unfortunately, 24 h later her visual fields deteriorated further and the patient underw...

ea0038p329 | Pituitary | SFEBES2015

Management of pituitary apoplexy: the greater Manchester experience

Giritharan Sumithra , Gnanalingham Kanna , Karabatsou Tina , Kearney Tara

Objective: To describe the experience of pituitary apoplexy from a single-centre modern series.Methods: We retrospectively reviewed the case notes of patients presenting to Salford Royal NHS Foundation Trust between February 2005 and April 2014 with pituitary apoplexy.Results: A total of 32 cases (20 males) presenting with classical apoplexy were identified, with a mean age at presentation of 54 years (range 22–88 years). 11 p...

ea0034p297 | Pituitary | SFEBES2014

Just another ‘incidental finding’?

Giritharan Sumithra , Kearney Tara , Doran Helen , Gnanalingham Kanna

A 60-year-old female was referred to the department in October 2010 after a CT thorax revealed an incidental finding of a right adrenal nodule. On questioning, the patient reported some sweats but otherwise no other symptoms of hormonal excess. Adrenal functional studies were normal and it was therefore decided that the patient should have a repeat CT scan in 6 months. Repeat CT adrenal glands in April 2011 did not show any changes to the size of the nodule but gave indetermin...