Searchable abstracts of presentations at key conferences in endocrinology

ea0092ps1-01-01 | Cancer | ETA2023

Impact of the 3rd edition of bethesda system for reporting thyroid cytopathology on grey zone categories

Guerreiro Sofia , Baran Yunus , Tavares Paula , Pinto Marques Hugo , Bongiovanni Massimo , Canberk Sule

First TBSRTC editions have made advances in problems of thyroid management. However, the real grey zone ‘AUS/FLUS’ and ‘FN/SFN’categories have been remained to be problematic with the wide range of ROMs documented in the literature alongside two editions. The ROMs of ‘AUS/FLUS’ and ‘FN/SFN’ categories were defined as 5-15% and 15-30% and the management was ‘repeat FNA’ and ‘lobectomy’ -respectively- in the first editi...

ea0049ep1373 | Thyroid (non-cancer) | ECE2017

Unilateral Graves’ disease with papillary carcinoma of the hyperfunctioning lobe

Papadakis Georgios , Rodriguez Elena Gonzalez , Allenbach Gilles , Lalonde Marie Nicod , Gorostidi Francois , Sandu Kishore , Bongiovanni Massimo , Sykiotis Gerasimos P.

Background: Graves’ disease (GD) typically manifests as an autoimmune hyperfunction of both thyroid lobes. Less than 10 cases of unilateral GD have been described, and the pathophysiology of unilateral GD remains unknown. Co-existence of malignancy has never been reported. We report a case of GD of the left lobe with simultaneous discovery of a papillary carcinoma within the hyperfunctioning lobe.Case description: A 49-year-old patient of Middle-Eas...

ea0070aep965 | Thyroid | ECE2020

Constitutive activation of Nrf2 antioxidant pathway leads to age-dependent goiter and compensated hypothyroidism in mice

Chartoumpekis Dionysios , Ziros Panos , Renaud Cédric , Bongiovanni Massimo , Habeos Ioannis , Liao Xiao-Hui , Refetoff Samuel , Kopp Peter , Brix Klaudia , Sykiotis Gerasimos

Background: KEAP1 gene (Kelch-like ECH-associated protein 1) that encodes the main inhibitor of nuclear factor erythroid 2-related transcription factor 2 (Nrf2), a central mediator of antioxidant responses, has been found to be one of the mutated genes that lead to familial multinodular goiter (MNG). The proposed association of KEAP1 with familial MNG is based on only two loss-of-function mutations in respective Japanese families. To date, there is no experim...