Searchable abstracts of presentations at key conferences in endocrinology

ea0079022 | Abstracts | BES2021

Isomorphic (KOEBNER) phenomenon induced by insulin injections in psoriasis: a case report

Saartje Thijs , Corinne Degraeve , Peter Coremans

Introduction: Lipohypertrophy is by far the most common skin-related complication of insulin therapy. Less common dermatological complications of insulin injections include lipoatrophy, localized allergic reaction, subcutaneous abscess, localized amyloidosis and hyperpigmentation of the skin at the site of injection. We describe the Koebner phenomenon in an insulin requiring type 2 diabetic patient during a psoriasis flare-up.Case report: A 56-year old w...

ea0081p36 | Calcium and Bone | ECE2022

Denosumab vs. zoledronic acid treatment in post-menopausal breast cancer: a 2-year prospective observational study

Buch-Larsen Kristian , Marina Djordje , Schwarz Peter

Adjuvant treatment for post-menopausal women with early breast cancer (BC) includes aromatase inhibitors (AI), known to decrease bone mineral density (BMD). In this study, we investigate whether denosumab is a valid second option for patients unable to receive standard adjuvant i.v. zoledronic acid (ZA). In total, 212 patients have been evaluated after they did not receive ZA. Of those 194 were included. After evaluation by an endocrinologist, all patients were offered ZA as t...

ea0050p222 | Diabetes and Cardiovascular | SFEBES2017

Screening for coeliac disease in type 1 DM – A retrospective observational study in Harrogate District Foundation Hospital

Shankaran Vani , Ray Sutapa , Hammond Peter

Coeliac disease is more common in people who have Type 1 diabetes mellitus (DM) because of their autoimmune co-existence. Between 4 and 9% of people with Type 1 DM will also have coeliac disease. The updated NICE guideline (NG 20 coeliac screening) recommends that adult with Type 1 DM should be tested for coeliac disease at diagnosis and retested if any symptoms of coeliac disease develop.Study method & Result: Newly...

ea0050p382 | Thyroid | SFEBES2017

A population-based study of the Epidemiology of Chronic Hypoparathyroidism

Vadiveloo Thenmalar , Donnan Peter , Leese Graham

Aim: We aimed to undertake a population-based approach to describing the prevalence and incidence of chronic hypoparathyroidism. There are very few reports on the epidemiology of this condition.Methods: Data linkage of all biochemistry, hospital admissions, prescribing and death records was undertaken in Tayside Scotland (population 400,000) from 1988 to 2015. Patients with at least 3 serum calcium concentrations below the reference range f...

ea0050p389 | Thyroid | SFEBES2017

Morbidity and Mortality in patients with Chronic Hypoparathyroidism

Vadiveloo Thenmalar , Donnan Peter , Leese Graham

Aim: We aimed to investigate mortality and morbidity in patients who were identified with primary hypoparathyroidism, post-surgical and non-surgical hypoparathyroidism.Methods: The patients who were previously identified with hypoparathyroidism, were linked to hospital admission dataset, renal registry, biochemistry dataset and prescribing dataset. In this study, death and 6 morbidities; cataract, circulatory system, infection, fracture, me...

ea0050p222 | Diabetes and Cardiovascular | SFEBES2017

Screening for coeliac disease in type 1 DM – A retrospective observational study in Harrogate District Foundation Hospital

Shankaran Vani , Ray Sutapa , Hammond Peter

Coeliac disease is more common in people who have Type 1 diabetes mellitus (DM) because of their autoimmune co-existence. Between 4 and 9% of people with Type 1 DM will also have coeliac disease. The updated NICE guideline (NG 20 coeliac screening) recommends that adult with Type 1 DM should be tested for coeliac disease at diagnosis and retested if any symptoms of coeliac disease develop.Study method & Result: Newly...

ea0050p382 | Thyroid | SFEBES2017

A population-based study of the Epidemiology of Chronic Hypoparathyroidism

Vadiveloo Thenmalar , Donnan Peter , Leese Graham

Aim: We aimed to undertake a population-based approach to describing the prevalence and incidence of chronic hypoparathyroidism. There are very few reports on the epidemiology of this condition.Methods: Data linkage of all biochemistry, hospital admissions, prescribing and death records was undertaken in Tayside Scotland (population 400,000) from 1988 to 2015. Patients with at least 3 serum calcium concentrations below the reference range f...

ea0050p389 | Thyroid | SFEBES2017

Morbidity and Mortality in patients with Chronic Hypoparathyroidism

Vadiveloo Thenmalar , Donnan Peter , Leese Graham

Aim: We aimed to investigate mortality and morbidity in patients who were identified with primary hypoparathyroidism, post-surgical and non-surgical hypoparathyroidism.Methods: The patients who were previously identified with hypoparathyroidism, were linked to hospital admission dataset, renal registry, biochemistry dataset and prescribing dataset. In this study, death and 6 morbidities; cataract, circulatory system, infection, fracture, me...

ea0082we5 | Workshop E: Disorders of the gonads | SFEEU2022

A challenging case of hypogonadism

Lei Yin Win , Witczak Justyna , Taylor Peter

Gonadal dysgenesis with DAX1 duplication as the cause of XY disorder of sexual development is a rare condition. Duplication of this causes male to female sex reversal while mutation or deletion can cause adrenal hypoplasia congenita with hypogonadotropic hypogonadism. We present a case of 37-year-old lady who was referred to endocrine clinic with ongoing symptoms of fatigue. She was diagnosed with 46 XY gonadal dysgenesis when she presented with groin swelling at the ...

ea0090ep221 | Calcium and Bone | ECE2023

Our experience with the treatment of pseudohypoparathyroidism

Pavaiova Anna , Pavai Dušan , Vanuga Peter

Pseudohypoparathyroidism (PHP) is a group of rare hereditary diseases caused by tissue resistance to parathyroid hormone (PTH), there are two main types I and II. Type I is divided into subtypes. The authors present a case of PHP Ib, with hypocalcemia (level of total calcium 1.41 mmol/l), accidentally detected at childbirth. After the unsuccessful treatment of hypocalcemia, the etiology was considered, but the confirmation of the diagnosis were not adequately tightened. Due to...