Abstract Library

#2218 More than Rare Pheochromocytomas: Bilateral and Hemorrhagic, Giant and Metastatic

Introduction: Pheochromocytomas (PCC) are rare neuroendocrine tumors. These catecholamine-secreting tumors, with an average size of 4.9cm, are multiple in 10% of cases. About 10% are malignant but distant metastases are rare. Non-traumatic adrenal hemorrhage is an unusual potentially fatal event seen in PCC.

Conference: 15th Annual ENETSConcerence (2018)

Presenting Author: Peralta Ferreira M

Authors: Peralta Ferreira M, Sousa Fernandes M, Roque R, Matos C, Strecht J,

Keywords: pheochromocytoma, giant, hemorrhagic, metastatic, bilateral,

#1530 Bizarre Neuroendocrine Tumour Presentations

Introduction: Herein we present two cases of neuroendocrine tumours (NET)with atypical presentations.

Conference: 13th Annual ENETSConcerence (2016)

Presenting Author: Palmela C

Authors: Palmela C, Cunha C, Costa Santos M, Glória L, Roque R,

Keywords: cutaneous metastasis, GI bleeding,

#1197 The Neuron-Specific Enolase Assessment in Patients with Neuroendocrine Tumors with or without Carcinoid Syndrome

Introduction: NeuroEndocrine Tumors (NETs) comprises a wide area of clinical presentations and neuroendocrine markers.

Conference: 12th Annual ENETSConcerence (2015)

Presenting Author:

Authors: Carsote M, Capatina C, Terzea D, Petris R, Goldstein A,

Keywords: neuron-specific enolase, neuroendocrine tumors,

#925 Negative Urinary Fractionated Metanephrines and Elevated Urinary Vanillylmandelic Acid in a Patient with a Sympathetic Paravesical Paraganglioma

Introduction: Paragangliomas have hereditary and sporadic presentations.

Conference: 11th Annual ENETSConcerence (2014)

Presenting Author:

Authors: Wandurraga E, Marín L,

Keywords: paraganglioma, pheochromocytoma, metanephrines, vanillylmandelic acid,

#829 On the Benign Side of Malignancy: How Neuroendocrine Tumors are Experienced by Patients and Their Family Carers

Introduction: Neuroendocrine tumors (NETs) are rare, slow-growing neoplasia with variable clinical presentations. Due to their non-specific symptoms and a lack of diagnostic tools, late diagnosis is common. There is little research relating to NETs as experienced by both patients and family carers.

Conference: 11th Annual ENETSConcerence (2014)

Presenting Author: Kall S

Authors: Kall S, Spichiger E, Stoll H,

Keywords: neuroendocrine tumors, rare diseases, qualitative research ,