Searchable abstracts of presentations at key conferences in endocrinology

ea0070ep582 | Hot topics (including COVID-19) | ECE2020

Graves’ disease following Hashimoto’s thyroiditis. Case report

Nduwayo Leonard , Marie Florence Niyitegeka

Hyperthyroidism in Graves’ disease (GD) is caused by thyroid-stimulating autoantibodies to the TSH receptor. Hypothyroidism in Hashimoto’s thyroiditis (HT) is associated with thyroid peroxidase and thyroglobulin autoantibodies. Transformation of HT to GD has been rarely reported. We report a woman with history of HT, who then developed GD.Case presentation: A 50-year-old female with a past history of hypothyroidism due to HT treated with Levo...

ea0012p117 | Steroids to include Cushing's | SFE2006

An audit of diagnosis and management of Cushing’s syndrome in a district general hospital

Farooq A , Abdalla TME , Wilton D , Wayte A , Griffiths K , Khan N , Wilton A

Cushing’s syndrome is a rare endocrine disorder which the Royal College of Physicians/Society for Endocrinology Guidelines – Pituitary Tumours (1997) suggest should only be differentially diagnosed in centres with appropriate technical and enocrinological expertise. We conducted an audit against these guidelines of the management of Cushing’s syndrome in our unit (population covered 250, 000) over the 3-year period between January 2003 and January 2006. Aetiolog...

ea0073aep123 | Calcium and Bone | ECE2021

Prevalence, characteristics, and associated factors of Fahr’s syndrome in permanent hypoparathyroidism

Cherchir Faten , Oueslati Ibtissem , Yazidi Meriem , Boukriba Seif , Chaker Fatma , Mizouni Habiba , Chihaoui Melika

IntroductionFahr’s syndrome (FS) is a rare neurodegenerative disorder. It’s characterized by abnormal calcifications in basal ganglia and cerebral cortex inducing neuropsychiatric disorders and cognitive impairment. The aim of our study was to assess the prevalence of FS, its characteristics, and its associated factors in patients with permanent hypoparathyroidism.MethodsWe conducted a cross-section...

ea0014p81 | (1) | ECE2007

Diabetic patient’s evaluation of continuous glucose monitoring sensors versus capillary glucose measurements

De Pinillos Gordillo Guilermo Martínez , Fernández-Argüelles Amaya , Garcí-Quirós Jm Juan Manuel

Objective: To evaluate the monitoritation systems acceptance: capillary glucose measurements and continuous glucose sensors (CGSM and GUARDIAN).Research design and methods: 15 diabetics patients were monitoritatied in two diferents periods of time. (Period 1: Guardian, 86 hours long. Period 2: CGSM 72 hours long). Later, they had to fill a satisfaction questionnaire concerning several aspects which were valued from 0–6.<table boarder="1" cellpad...

ea0073aep838 | Late Breaking | ECE2021

Consecutive development of adrenal Cushing´s syndrome and Cushing´s disease in a female patient with somatic CTNNB1, USP8, and NR3C1 mutations

Detomas Mario , Altieri Barbara , Schlötelburg Wiebke , Appenzeller Silke , Sven-Martin Schlaffer , Roland Coras , Andreas Schirbel , Wild Vanessa , Kroiss Matthias , Sbiera Silviu , Fassnacht Martin , Deutschbein Timo

ContextThe occurrence of different subtypes of endogenous Cushing’s syndrome (CS) in single individuals is extremely rare. We here present the case of a female patient who was successfully cured from adrenal CS 4 years before being diagnosed with Cushing’s disease (CD).Case DescriptionA 50-year-old female was diagnosed with ACTH-independent CS and a left-sided adrenal adenoma in January 2015. After ...

ea0075p13 | Pituitary and neuroendocrinology | EYES2021

Consecutive adrenal cushing´s syndrome and cushing´s disease in a patient with somatic CTNNB1, USP8, and NR3c1 mutations

Detomas Mario , Altieri Barbara , Schlotelburg Wiebke , Appenzeller Silke , Schlaffer Sven , Coras Roland , Schirbel Andreas , Wild Vanessa , Kroiss Matthias , Sbiera Silviu , Fassnacht Martin , Deutschbein Timo

Context: The occurrence of different subtypes of endogenous Cushing’s syndrome (CS) in single individuals is extremely rare. We here present the case of a female patient who was successfully cured from adrenal CS 4 years before being diagnosed with Cushing&apos;s disease (CD).Case Description: A 50-year-old female was diagnosed with ACTH-independent CS and a left-sided adrenal adenoma in January 2015. After adrenalectomy and histopathological co...

ea0070aep938 | Thyroid | ECE2020

Severe hypothyroidism secondary to Hashimoto’s thyroiditis and its implications for surgery

Yu Xinming , Soong Elaine , Li Mengye , Majeed Joohi

Background: The prevalence of hypothyroidism is around 1–2% in the UK. Hashimoto’s thyroiditis is thought to cause 0.1–2% of overt disease and 10–15% of subclinical hypothyroidism. This case presents a patient with severe hypothyroidism, secondary to Hashimoto’s thyroiditis, found incidentally on a surgical admission. The case study discusses the challenges and management of severe hypothyroidism in the need for an acute surgical intervention....

ea0070aep1088 | Hot topics (including COVID-19) | ECE2020

Cushing’s disease recurrence during peripartum period: A case report

Fellipe Carvalho Viola Luiz , Muniz Raquel , Stefanello Lariana , Massucati Negri Maurício , Warszawski Leila

Introduction: Even with a high incidence of infertility owing to the suppressive effects of hypercortisolism in the gonadal axis, either associated or not to hyperandrogenism and ovulatory dysfunction, Cushing’s syndrome (CS) during pregnancy has been reported. This could be due to a greater rate of CS among women in reproductive age; however, it is a rare condition, with fewer than 200 cases reported in the literature. In general, CS affects 2–25 people to every 1...

ea0013p78 | Clinical practice/governance and case reports | SFEBES2007

Apparent hypopituitarism secondary to Cushing’s syndrome due to adrenal carcinoma

Revesz Sarah , Knox Andrew , Vaidya Bijay

A 75-year-old lady presented with hypertension, weight gain, ankle oedema and proximal myopathy. She had clinical features of Cushing’s syndrome. Blood pressure was 180/99 mmHg. Her visual fields were normal. Investigations confirmed Cushing’s syndrome with high 24-hour free urinary cortisol levels (2264 nmol/l and 3295 nmol/l; normal range 40–305) and a high serum cortisol level following overnight dexamethasone suppression test (serum cortisol 1,550 nmol/l). F...

ea0073aep379 | Endocrine-Related Cancer | ECE2021

Ectopic cushing’s syndrome due to an acinic type parotid carcinoma

Zerva Dimitra , Pappa Dimitra , Mparmpa Eleftheria , Anastasia –Κonstantina Sakali , Thoda Pinelopi , Georgiou Eleni , Gountios Ioannis , Alexandra Bargiota

IntroductionEctopic Cushing’s syndrome(ECS) is responsible for 15–20% of all cases of ACTH dependent Cushing’s syndrome. We present here a very rare case of ECS due to an acinic parotid carcinoma (ACC).PresentationA 44 year old woman with a medical history of metastatic ACC parotid carcinoma and type 1 diabetes mellitus (T1DM), referred to our department, due to cushingoid features, progressive...