Searchable abstracts of presentations at key conferences in endocrinology

ea0037ep578 | Obesity and cardiovascular endocrinology | ECE2015

A 5-year review of the metabolic changes after laparoscopic sleeve gastrectomy among obese Hong Kong Chinese in a regional hospital

Ho Cheuk Wah , Kam Grace , Tsang Man Wo

Background and aims: Obesity is a global problem. Laparoscopic sleeve gastrectomy (LSG) was introduced in our hospital since 2008. This study aimed at reviewing the metabolic changes after LSG among Hong Kong Chinese in a regional hospital.Materials and methods: 47 patients who received LSG in our hospital from June 2008 to October 2012 were retrospectively reviewed. Change in body weight (BW) and glycaemic control up to 5 years were evaluated. Rate of r...

ea0090p387 | Endocrine-related Cancer | ECE2023

Don’t let your guard down – aggressive, hereditary paraganglioma associated with SDHD gene nonsense variant: c.33C>A (p.(Cys11Ter))

Szatko Alicja , Leszczynska Dorota , Woźniak Beata , Papierska Lucyna , Zgliczyński Wojciech , Glinicki Piotr

Introduction: Paragangliomas belong to the neuroendocrine tumours arising from autonomic nervous system. Various localizations, symptoms that can mimic a wide range of diseases and often unpredictable ability to metastasize are the reasons why paragangliomas pose a significant diagnostic challenge. More than one third of paragangliomas is associated with germline mutations –succinate dehydrogenase (SDH) subunit genes are among the most common susceptibility genes. SDHD wa...

ea0070aep26 | Adrenal and Cardiovascular Endocrinology | ECE2020

Genetic alterations and clinical features in 16 brazilian patients with pheochromocytomas and paragangliomas

Naliato Erika , Araujo Paula , Soares Paula , Lima Jorge , Lima Vinicius , Wo Julia , Sanchez Mirna , Carvalho Denise , Violante Alice

Introduction: Pheochromocytomasand paragangliomas are tumors derived from chromaffin cells which result from mutations of at least six different genes as autosomal dominant disorders.Aim: To evaluate the existence of correlations between genetic alterations and clinical data in 16 patients with pheochromocytomas and/or paragangliomas.Methods: From 2007 to 2009, 13 patients with pheochromocytoma [3 men, medium age 39 years (14&#8211...

ea0049oc9.3 | Thyroid Disease 2 | ECE2017

How much of the genetic predisposition to Hashimoto’s thyroiditis can be explained by genes commonly associated with the disease?

Skalniak Anna , Jabrocka-Hybel Agata , Piętkowski Jakub , Turek-Jabrocka Renata , Pach Dorota , Ludwig-Gałęzowska Agnieszka , Machlowska Julita , Kapusta Przemysław , Wołkow Paweł , Hubalewska-Dydejczyk Alicja

Background: Hashimoto’s thyroiditis (HT) is a common autoimmune disorder of the thyroid (AITD) which affects about 1–2% of the European population. The disease often clusters in families, which is why many attempts have been undertaken to find the genetic background that would underly the predisposition to HT. In contrast to another AITD - Graves’ disease, results of genetic analyses have been ambiguous and have failed to find a major genetic locus that would be...