Abstract Library

#4321 Insulinoma – A diagnostic challenge

Introduction: Insulinomas are rare pancreatic neuroendocrine neoplasms (pNEN). Operative resection is the treatment of choice.

Conference:

Presenting Author:

Authors: Ritter A, Poppinga J, Steinkraus K, von Kroge P, Amin T,

Keywords: Neuroendocrine neoplasia, insulinoma, pancreatic NEN, hypoglycaemia,

#3728 ACTH-secreting pancreatic neuroendocrine neoplasms – A case-series

Introduction: Ectopic Cushing’s syndrome occurs rarely in patients with pancreatic neuroendocrine neoplasms. Early recognition of symptoms is critical given the high morbidity and mortality associated with Cushing’s syndrome.

Conference:

Presenting Author: Al-Toubah T

Authors: Al-Toubah T, Pelle E, Hallanger-Johnson J, Haider M, Strosberg J,

Keywords: pancreatic neuroendocrine neoplasm, Cushing’s syndrome, ACTH, ectopic Cushing’s, neuroendocrine tumor,

#3307 Heterogenic clinical manifestation of hypoglycaemia in patients with insulinoma

Introduction: Insulinomas are very rare neuroendocrine tumors. Clinically, these tumors are manifested by episodes of hypoglycaemia. Classically, these symptoms are called as "Whipple's triad" and include symptoms of hypoglycaemia, low glycaemia, and disappearance of these difficulties after glucose ingestion. Recognition of clinical symptomatology of hypoglycaemia is essential for early diagnosis and treatment.

Conference: 18th Annual ENETS Concerence (2021)

Presenting Author: Nosakova L

Authors: Nosakova L, Bánovčin P, Uhrík P, Ďuríček M, Pindura M,

Keywords: insulinoma, hypoglycaemia, clinical signs,

#1414 Non-functioning Adrenal Composite Pheochromocytoma-Ganglioneuroma Simultaneous with Subclinical Cushing's Syndrome Due to Contralateral Adrenal Hyperplasia - An Unusual Presentation

Introduction: “Composite” pheochromocytoma is a rare tumor, consisting of pheochromocytoma and neuroblastic tumors. The definite diagnosis is histological. Subclinical Cushing's syndrome refers to autonomous glucocorticoid production without specific signs and symptoms of Cushing's syndrome.

Conference: 13th Annual ENETSConcerence (2016)

Presenting Author: Kiraly A

Authors: Kiraly A, Muntean V, Domsa I, Ghervan C,

Keywords: adrenal, composite, pheochromocytoma, ganglioneuroma, hypercorticism.,

#1329 The MEN2B Due to de Novo Mutation M918T at Algiers

Introduction: The MEN2B, or Gorlin syndrome is a very rare disorder where there are a medullary cancer of thyroide associated with pheochromocytoma and other clinical signs such as a ganglion – neuromatose or a Marfan syndrome. The MEN2B belongs MEN2 are rare hereditary disease, transmitted as an autosomal dominant mutations linked to the RET proto-oncogene.

Conference: 13th Annual ENETSConcerence (2016)

Presenting Author:

Authors: Chikouche A,

Keywords: MEN2B, de novo mutation, genotypic analysis,