Searchable abstracts of presentations at key conferences in endocrinology

ea0011p636 | Neuroendocrinology and behaviour | ECE2006

The incidence of spontaneous cerebro-spinal fluid rhinorrhea in a large series of patients with macroprolactinoma

Suliman SGI , Byrne J , Ansorge O , Wass JAH

Cerebro-spinal fluid (CSF) rhinorrhea is a recognised complication of pituitary surgery, and occasionally occurs following pituitary radiotherapy. Macroprolactinomas (MPRL) may result in spontaneous or dopamine-agonist-induced CSF leaks, however no detailed large comparisons have been made with non-functioning adenomas (NFA). The incidence of this phenomenon and the mechanisms underlying it are not understood.We have performed a retrospective review of s...

ea0013p244 | Neuroendocrinology and behaviour (including pituitary) | SFEBES2007

Non-surgical cerebro-spinal fluid rhinorrhea in invasive macroprolactinoma: incidence, radiological and clinicopathological features

Suliman SGI , Gurlek A , Byrne J , Sullivan N , Thanabalasingham G , Cudlip S , Ansorge O , Wass JAH

Objective: Macroprolactinomas (MPRL) may result in spontaneous or dopamine-agonist-induced CSF rhinorrhoea. The incidence of, and mechanisms underlying this phenomenon are poorly understood. In this study, we aimed to determine the incidence of non-surgical (spontaneous and dopamine-agonist-induced) rhinorrhoea, and to identify biochemical, radiological and histopathological factors associated with this phenomenon.Methods: We retrospectively reviewed MPR...

ea0011p159 | Clinical case reports | ECE2006

Not-so-silent, silent corticotroph adenomas

Suliman SGI , Baldeweg SE , Ansorge O , Clark A , Powell M , Wass JAH

Late onset Cushing’s disease, occurring years following the diagnosis of a silent corticotroph adenoma (SCA) is rare, with very few previously reported cases. We present a series of 5 subjects with SCA, aggressive tumour recurrences and late onset Cushing’s disease.The mean age of subjects at initial presentation was 41 yrs (35–52), sex 3:2 (M:F). There were no clinical features of hypercortisolism at diagnosis. Two subjects had hypocortis...