Abstract Library

#4577 Diagnosis of a cervical carotid paraganglioma: A case report and review of diagnostic imaging approaches

Introduction: Cervical paragangliomas are rare, often non-secreting tumours of neuroectodermal origin. Their diagnosis can be challenging due to the variability of clinical presentations and the diagnostic tests required.

Conference:

Presenting Author: Otmane R

Authors: Otmane R, Boudersa A, Kouadri N,

Keywords: Paraganglioma, cervical, octreoscan,

#3570 Metastatic middle ear neuroendocrine tumor treated with Somatostatin analogues and PRRT – A case report

Introduction: Neuroendocrine adenomas of the middle ear (NEAME) are rare tumors. They have mostly indolent biological behaviour, however, reports of an aggressive course and metastasis have been described.

Conference:

Presenting Author: Gomes Martins R

Authors: Elvas A, Magalhães J, Monteiro J, Barros J, Rei L,

Keywords: Neuroendocrine adenomas of the middle ear, somatostatin analogues, peptide receptor radionuclide therapy,

#3286 MEN1 syndrome and neuroendocrine tumor of unknown primary

Introduction: Multiple Endocrine Neoplasia type 1 (MEN1) is a hereditary condition associated with tumors of endocrine glands. NeuroEndocrine Neoplasms (NENs) are characterized as rare neoplasms.

Conference: 18th Annual ENETS Concerence (2021)

Presenting Author: Tsoukalas N

Authors: Tsoukalas N, Sakellaridis T, Kyriakopoulos G, Arvanitou E, Tsitsimpis A,

Keywords: neuroendocrine neoplasm, multiple endocrine neoplasia type 1 (MEN1), unknown primary, atypical carcinoid of thymus,

#3150 A case report of familial paraganglioma syndrome type 4 caused by the SDHB mutation gene

Introduction: Paraganglioma type 4 syndrome is associated with SDHB mutation with a higher risk of malignancy.

Conference: 18th Annual ENETS Concerence (2021)

Presenting Author:

Authors: Ciobanu O, Lambrescu I, Leca B, Nistor I, Martin S,

Keywords: paraganglioma, sdhb mutation,

#1640 SDHB Mutation in a Young Patient with a Metastatic Paraganglioma of the Urinary Bladder

Introduction: Paragangliomas are rare tumors that arise from the sympathetic and parasympathetic ganglia that can possess an inherited trait.

Conference: 14th Annual ENETSConcerence (2017)

Presenting Author:

Authors: Lambrescu I, Cima L, Leca B, Martin S, Fica S,

Keywords: paragangliomas, SDHB mutation,