Abstract Library

#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,

#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,

#3632 Medullary thyroid carcinoma and somatostatin analogues, a possible therapeutic choice in asymptomatic and slow radiological progression metastatic recurrent disease after surgery – Case report of a 22-years long term survival patient

Introduction: Medullary thyroid carcinoma (MTC) is a well-differentiated neuroendocrine tumor of the thyroid and accounts for 1%-2% of thyroid cancers in the United States. MTCs present with locoregional metastasis in 50% of patients and distant metastasis in 10%-15% at diagnosis. Treatment options for recurrent or progressive disease according to RECIST 1.1 criteria, are limited. Tyrosine kinase-inhibitors (TKI) are preferred as first-line systemic therapy. Although somatostatin analogues (SSA) may play a role in MTC, limited evidence is available.

Conference:

Presenting Author: Raia S

Authors: Raia S, Chiloiro S, Maratta M, Giampietro A, de Marinis L,

Keywords: medullary thyroid carcinoma (MTC), somatostatin analogues, survival,

#3538 A challenging diagnosis of a neuroendocrine tumor of unknown origin associated with primary aldosteronism

Introduction: Neuroendocrine tumors (NETs) of unknown primary site account for 10 to 14 percent of all neuroendocrine neoplasms.

Conference:

Presenting Author: Ciobanu O

Authors: Ciobanu O, Martin S, Fica S,

Keywords: neuroendocrine tumor, unknown origin, primary hyperaldosteronism, challenging diagnosis,

#3496 Children with Primary Hyperparathyroidism After Parathyroidectomy

Introduction: Surgical treatment is the radical and most effective treatment for primary hyperparathyroidism (PHP). According to a number of studies, it has been shown that parathyroidectomy leads to an improvement in the quality of life in patients.

Conference:

Presenting Author:

Authors: Rixsieva N, Ismailov S,

Keywords: primary hyperparathyroidism, parathyroidectomy, children, quality of life,