Searchable abstracts of presentations at key conferences in endocrinology
Previous issue | Volume 102 | EYES2024

ESE Young Endocrinologists and Scientists (EYES) 2024

ea010229 | Interdisciplinary Endocrinology | EYES2024

Similar recurrence and survival in pre- and post-renal transplant papillary thyroid cancer: data from a 1507 recipient registry

Turkum Atikcan Deniz , Gul Kose Hamidi Ece , Senturk Mustafa , Turhan Iyidir Ozlem , Nar Aslı , Bascil Tutuncu Neslihan , Haberal Mehmet

Introduction: Thyroid nodules discovered during pre-transplant evaluation may delay the transplantation process. While studies suggest an increased incidence of thyroid cancer following solid organ transplantation, the impact on prognosis in papillary thyroid cancer (PTC) among renal transplant recipients remains unclear.Methods: We conducted a retrospective review of renal transplant recipients with a history of PTC at our institution between 1998 and 2...

ea0102129 | Interdisciplinary Endocrinology | EYES2024

Retinal microvascular changes with OCT angiography and serum gremlin-1 levels in acromegaly: a case-control study

Unal Kocabaş Gokcen , Kuşat Damla , Furundaoturan Onur , Değirmenci Cumali , Ozgur Su , Şarer Yurekli Banu

Introduction: Increased GH and IGF-1 levels in acromegaly results in several micro and macrovascular changes. There are controversial results about the effects of GH/IGF-1 on retinal vasculature. Gremlin-1 is a BMP-4 antagonist which binds to VEGFR to activate its pathway and has demonstrated angiogenic properties on several tissues. We aimed to detect retinal changes in acromegaly and examine its association with serum gremlin-1 levels.Methods: We inclu...

ea010251 | Interdisciplinary Endocrinology | EYES2024

Putting two and two together: a rare case of mccune-albright syndrome

Luca Celina , Popescu Diana-Ioana , Chelaru Nicoleta , Adam Viviana-Elena , Iancu Ionut-Daniel , Vasiliu Ioana , Preda Cristina , Cristea Cristina

Introduction: McCune-Albright syndrome (MAS) is a rare genetic disorder caused by somatic gain-of-function mutations in the GNAS gene, leading to persistent activation of the stimulatory alpha subunit of the G protein cellular signaling complex and dysregulated cyclic AMP production in the target tissues. The phenotype, although highly variable, is classically defined as the triad of fibrous dysplasia of the bone, cafe-au-lait skin macules and hyperfunctioning endocrinopathies...

ea010249 | Interdisciplinary Endocrinology | EYES2024

Revealing fahr’s syndrome in a patient previously misdiagnosed and treated for epilepsy: a case report

Mikaberidze Ana , Gabidzashvili Nino , Nakaidze Nana , Dophidze Elene , Ambriashvili Kristine , Vinogradskaya Olga , Dushashvili Ioseb , Gzirishvili Nino , Vadachkoria Tamar

Introduction: Hypoparathyroidism with abnormal calcium deposits in the basal ganglia is known as Fahr’s syndrome, a rare condition affecting fewer than 1 in 1,000,000 people, typically those aged 40-60. In contrast, Fahr’s disease is characterized by isolated brain calcification without underlying metabolic or endocrine disorders. Both conditions often manifest with neurological and cognitive disorders, seizures, and sometimes psychosis. However, symptoms of Fahr&#14...

ea0102136 | Interdisciplinary Endocrinology | EYES2024

In vitro evaluation of the HEK293 cell line as a model to measure glucocorticoids activity

Rossi Lucrezia , Rosaria Ambrosio Maria , Marino Picciola Valentino , Bordignon Anna , Chiara Zatelli Maria

Introduction: Glucocorticoids (GCs) are closely related to cortisol and the dysregulation of its secretion can lead to the onset of disorders. Cushing’s syndrome (CS) is the clinical manifestation of hypercortisolism and can also develop in subjects who voluntarily or accidentally take high GCs doses. The aim of this study is to conduct preliminary investigations to characterize the HEK293 cell line, to evaluate its response to GCs and to compounds with GC-like activity.<...

ea0102132 | Interdisciplinary Endocrinology | EYES2024

Complexity and multimorbidity in autoimmune polyendocrine syndrome type 2 – a case report

Ziobro Lidia , Suchy Wiktoria

Introduction: Autoimmune polyendocrine syndrome type 2 (APS-II) is characterized by the presence of at least two of the following autoimmune disorders: Addison’s disease, and autoimmune thyroid disease or diabetes mellitus. It is the most prevalent form of autoimmune polyendocrine syndrome and can be accompanied by other autoimmune disorders, leading to a range of clinical pictures. Case description: We present the case of a 57-year-old woman with a...