Abstract Library
Welcome to the open-access search for all ENETS abstracts presented at the Annual ENETS Conferences.
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ENETS Abstract Search
#4608 A complex and rare association of neuroendocrine and endocrine neoplasms: A case report
Introduction: Neuroendocrine tumours (NETs) are sporadic or genetically inherited heterogenous neoplasms affecting multiple sites.
Conference:
Presenting Author: Cerroni L
Authors: Cerroni L, Filice A, Feola T, Sesti F, Vincenzi L,
Keywords: cushing disease, atypical carcinoid, ileal net, genetics,
#4606 Neuroendocrine mess – Ectopic Cushing syndrome and severe hypokalaemia
Introduction: Cushing Syndrome (CS) is the condition resulting from hypercortisolaemia. Ectopic Cushing Syndrome (ECS) is responsible for up to 20% of all CS cases. Pancreatic neuroendocrine neoplasms (pNEN) are responsible for 10-20% of those cases.
Conference:
Presenting Author:
Authors: Corrêa Figueira C, Alves H, Bento A, Cardoso Gomes C, Oliveira A,
Keywords: Pancreatic neuroendocrine neoplasm, Hepatic neuroendocrine metastasis, Paraneoplastic syndrome, Cushing syndrome, Ectopic Cushing syndrome,
Introduction: The most common side effect of radioligand therapy is renal damage, early or late. However, limited data exist for the long-term side effects and impact of additional risk factors on renal function in patients treated with PRRT.
Conference:
Presenting Author: Sygula A
Authors: Sygula A, Kropinska A, Kotecka-Blicharz A, Gawlik T, Wycislik M,
Keywords: Neuroendocrine tumour, PRRT, nephrotoxicity, yttrium-90, lutetium-177,
Introduction: PRRT an established treatment for neuroendocrine tumours (NETs). Therapy requires prophylactic positively charged amino acid (AA) co-infusion to reduce renal radiation exposure. AA infusion has been associated with metabolic acidosis and electrolyte abnormalities, particularly hyperkalaemia; comprehensive data on the prevalence and severity of these complications remains limited.
Conference:
Presenting Author:
Authors: Osher E, Wolf I, Geva R, Sofer Y, Greenman Y,
Keywords: PRRT, hyperkalaemia, amino acid infusion, neuroendocrine tumour, adverse effects,
#4317 Late diagnosis of MEN2A syndrome: Ten cases in one family
Introduction: Multiple endocrine neoplasia type 2 (MEN2) constitutes a rare hereditary cancer syndrome affecting various endocrine glands.
Conference:
Presenting Author:
Authors: Asanova A, Shutova A, Dzeranova L, Przhiyalkovskaya E, Pigarova E,
Keywords: MEN2A, RET, MTC, THYROIDECTOMY,