Searchable abstracts of presentations at key conferences in endocrinology

ea0034p303 | Pituitary | SFEBES2014

Differential p120 isoform distribution and splicing regulator ESRP1 expression distinguishes sparsely and densely granulated somatotroph adenomas

Larkin Sarah , Ansorge Olaf

Somatotroph adenomas (SA) causing acromegaly are histologically classified into densely (DG) and sparsely granulated (SG) subtypes. We1 and others have shown that these histological subtypes may be clinically relevant. In short, SGSAs are generally found in younger, mainly female patients. They are larger at presentation, more invasive and show higher proliferation indices compared with DGSAs. Fibrous bodies (FBs) are the histological hallmark of SGSAs; they consist...

ea0044p132 | Neoplasia, cancer and late effects | SFEBES2016

Sparsely granulated somatotroph adenomas display aspects of epithelial-mesenchymal transition

Dix Kathryn , Grossman Ashley , Ansorge Olaf , Larkin Sarah

Somatotroph adenomas (SA) causing acromegaly exist as two major pathological variants: densely and sparsely granulated, according to the number and distribution of growth-hormone-containing secretory granules. These variants are increasingly recognised by neuropathologists and endocrinologists, but the consequences for tumour behaviour and patient outcome remain to be defined. Sparsely granulated SAs are associated with younger, female patients and are more invasive and prolif...

ea0019p190 | Endocrine tumours and neoplasia | SFEBES2009

Expression of guanylyl cyclase-B (GC-B) receptors in a range of human pituitary adenomas: evidence for a local natriuretic peptide system

Thompson I , Ansorge O , Karavitaki N , Wass J , Fowkes R

Several recent studies have identified Npr2 gene mutations (encoding the guanylyl cyclase B (GC-B) receptor) as causing dwarfism and achondroplasia. Npr2 null mice have a similar bone phenotype, pituitary growth hormone deficiency and female infertility. As the endogenous ligand for GC-B, C-type natriuretic peptide (CNP) is expressed at high levels in the anterior pituitary of rats and mice, we examined whether components of the natriuretic peptide system were al...

ea0012p7 | Clinical case reports/Governance | SFE2006

Anaplastic astrocytoma co-existing with acromegaly: the first report

Karavitaki N , Fazal-Sanderson V , Ansorge O , Wass JAH

Co-existence of a brain tumour (not associated with previous irradiation) and a pituitary adenoma has been rarely described. Astrocytomas have an incidence of <5/100,000 and somototroph adenomas of <4/1,000,000. In astrocytomas, a positive correlation between IGF-I immunoreactivity and histopathological grade/cell proliferation rates have been proposed. Here, we report a case of acromegaly detected incidentally shortly after the diagnosis of an anaplastic astrocytoma.<...

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...

ea0009p110 | Endocrine tumours and neoplasia | BES2005

Symptomatic Rathke cleft cysts: systematic review of 10 cases with long follow-up

Karavitaki N , Georgas G , Ansorge O , Adams C , Wass J

Background: Rathke cleft cysts (RCC) are benign, epithelial-lined cystic lesions arising from remnants of Rathke's pouch. Although reported in 13-22% of normal autopsies, they are rarely symptomatic. Their outcome after surgery remains unclear.Aim: To analyse the clinical/laboratory features and treatment outcome of patients who presented to the Departments of Endocrinology and Neurosurgery with symptomatic RCC (histologically confirmed) between 1977-200...

ea0009p122 | Endocrine tumours and neoplasia | BES2005

Lymphocytic hypophysitis: What is the long-term outcome?

Tsametis C , Karavitaki N , Ansorge O , Turner H , Wass J

BACKGROUND: Lymphocytic hypophysitis (LHy) is an uncommon inflammatory disorder of the pituitary with features mimicking those of sellar tumours, thereby often being misdiagnosed. However, no long-term follow-up studies have been published.OBJECT: To evaluate the clinical/radiological characteristics and the prognosis of patients with LHy.PATIENTS-METHODS: The records of the patients who presented to the Department of Endocrinology...

ea0007p265 | Clinical case reports | BES2004

Cushing's disease and coexistent craniopharyngioma - report of a case

Karavitaki N , Hull R , Ansorge O , Brufani C , Wass J

Craniopharyngiomas are tumours of the squamous epithelium, which arise in the sellar and/or suprasellar regions from embryonic squamous cell rests of the involuted hypophyseal-pharyngeal duct. They account for approximately 3% of intracranial neoplasms, present with symptoms relating to pressure effects on adjacent organs and often have an unpredictable behaviour. Corticotroph adenomas, usually measuring a few millimeters in diameter, are found in 10-12% of surgically removed ...

ea0050ep067 | Neuroendocrinology and Pituitary | SFEBES2017

A case of plurihormonal TSHoma presenting as meningitis

Khan Shoaib , Grossman Ashley , Cudlip Simon , Mohammadi Bahram Jaffar , Ansorge Olaf , Pal Aparna

This 22 year old lady presented with Haemophilus Influenza meningitis. Given an unusual organism, she had an MRI which revealed an incidental pituitary macroadenoma extending into the right cavernous sinus and breaching the anterioinferior wall of the pituitary fossa. Thyroid function showed raised T4 (24.7 pmol/L) and T3 (8.3 pmol/L) with unsuppressed TSH (1.75 munit/L). IGF-1 was also raised at 56.7 nmol/L (12–50.1 nmol/L).<p c...

ea0050ep067 | Neuroendocrinology and Pituitary | SFEBES2017

A case of plurihormonal TSHoma presenting as meningitis

Khan Shoaib , Grossman Ashley , Cudlip Simon , Mohammadi Bahram Jaffar , Ansorge Olaf , Pal Aparna

This 22 year old lady presented with Haemophilus Influenza meningitis. Given an unusual organism, she had an MRI which revealed an incidental pituitary macroadenoma extending into the right cavernous sinus and breaching the anterioinferior wall of the pituitary fossa. Thyroid function showed raised T4 (24.7 pmol/L) and T3 (8.3 pmol/L) with unsuppressed TSH (1.75 munit/L). IGF-1 was also raised at 56.7 nmol/L (12–50.1 nmol/L).<p c...