Searchable abstracts of presentations at key conferences in endocrinology

ea0032p909 | Pituitary – Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2013

PONV prophylaxis alters postoperative cortisol-measurement in transphenoidal pituitary surgery

Burkhardt Till , Rotermund Roman , Kiefmann Rainer , Westphal Manfred , Flitsch Jorg

Objective: Postoperative nausea and vomiting is common after general anaesthesia and is reported by ~20–25% of all patients. The standard prophylaxis at the authors department is a single treatment of 4 mg of dexamethasone before initiating anesthesia. Dexamethasone is known to suppress ACTH and cortisol levels. The objective was to find out whether the standard PONV-prophylaxis of 4 mg of dexamethasone has an effect on postoperative levels of cortisol in patients undergo...

ea0041ep899 | Pituitary - Clinical | ECE2016

Surgical Treatment and outcome of TSH-producing pituitary adenoma

Burkhardt Till , Rotermund Roman , Sauer Nina , Matschke Jakob , Schmidt Nils-Ole , Flitsch Jorg

Objectives: TSH-producing pituitary adenomas account for 1–2% of all pituitary tumors and there is debate wether transsphenoidal surgery or medical treatment should be recommended as first-line treatment. This study summarizes the authors surgical experience and puts it into context of literature concerning non-surgical treatment of TSHomas.Methods: A retrospective analysis of 12 patients including imaging, laboratory testing, short-term and long-te...

ea0035p581 | Endocrine tumours and neoplasia | ECE2014

Is early repeat surgery a feasible concept for potential incomplete resection in acromegaly?

Rotermund Roman , Lautenbach Anne , Burkhardt Till , zur Wisch Clarissa Schulze , Aberle Jens , Flitsch Jorg

Transsphenoidal surgery is the treatment of choice for acromegaly. Cure is defined by normalization of age-related IGF1 and sufficient suppression of GH in the oral glucose tolerance test (OGTT). We investigated, if early postoperative hormone testing gives reliable information whether complete resection of a tumor was achieved and compared these findings with further follow-up data.So far, 22 patients underwent OGTT within a week after surgery, starting...

ea0070yi4 | Young Investigators | ECE2020

Evidence for increased SSTR5 expression and improved pasireotide response in USP8 mutant corticotroph tumours

Albani Adriana , Perez-Rivas Luis Gustavo , Sicheng Tang , Buchfelder Michael , Rotermund Roman , Flitsch Jörg , Losa Marco , Stalla Günter , Reincke Martin , Theodoropoulou Marily

The somatostatin analogue pasireotide is approved for the treatment of Cushing’s disease, where it achieves biochemical normalization in ~40% of patients. Predicting pasireotide resistance would help avoid unnecessary treatment. Pasireotide mediates its antisecretory action by binding to somatostatin receptor 5 (SSTR5). Almost half of corticotroph tumours carry mutations in the ubiquitin specific protease 8 (USP8) gene that encodes for a deubiquitinase. Pre...

ea0073oc8.1 | Oral Communications 8: Pituitary and Neuroendocrinology | ECE2021

Expression and putative role of 14–3-3 proteins in corticotroph tumours

Tang Sicheng , Perez-Rivas Luis Gustavo , Albani Adriana , Rotermund Roman , Flitsch Jörg , Honegger Jürgen , Rachinger Walter , Sigrun Röber , Herms Jochen , Reincke Martin , Theodoropoulou Marily

IntroductionSomatic USP8 mutations are found in around 50% of Cushing’s disease tumours and are located in a single mutational hotspot that contains the recognition site for 14–3-3. These proteins bind to phosphoserine recognition motifs to alter the function and location of their target proteins, and are deregulated in several cancers. AimTo explore the expression and function of 14–3-3 prot...

ea0073oc13.1 | Oral Communications 13: Pituitary and Neuroendocrinology | ECE2021

TP53 mutations in functional corticotroph tumours: prevalence and clinical relevance

Perez-Rivas Luis Gustavo , Simon Julia , Albani Adriana , Rotermund Roman , Hermus Perez-Rivas , Guillaume Assié , Gadelha Monica , Deutschbein Timo , Flitsch Jörg , Honegger Jürgen , Rachinger Walter , Stalla Günter , Reincke Martin , Theodoropoulou Marily

IntroductionTP53 mutations have been rarely reported in pituitary tumours. Recently two exploratory exome sequencing studies have identified somatic TP53 mutations in a small number of functional corticotroph tumours (6/18 and 4/10) with USP8 wild type (wt) status, suggesting that they may be more frequent than previously thought. Nevertheless, the clinical impact of those mutations is still unknown.AimTo det...