#4218
Primary hepatic neuroendocrine tumor in a series of 8 cases
Introduction:
Primary neuroendocrine (NET) tumors of the liver are extremely rare, accounting for 0.3% of all NETs; unlike metastatic neuroendocrine tumors, rarely cause carcinoid syndrome. Edmonson reported the first case in 1958. Since then, fewer than 150 cases have been reported in the literature. Before making the diagnosis of primary hepatic neuroendocrine tumor it is imperative to explore the patients, several radiological investigations can help to pinpoint the primary which is most often digestive.
Conference:
Presenting Author:
Authors:
Samia K,
Fatima H,
Benali T,
Nabil B,
Aisha B,
Keywords:
neuroendocrine tumor,
primary,
hepatic,
metastasis,
rare,
neuroendocrin carcinoma,
#4142
Metastatic insulinoma – A clinical conundrum
Introduction:
We present a case series of metastatic insulinoma from a single tertiary referral centre, highlighting heterogeneity in presentations, management, and multimodal therapy.
Conference:
Presenting Author:
Authors:
Mathara Diddhenipothage S,
Matheou M,
Wilson S,
Naseer A,
Moore N,
Keywords:
Metastatic insulinoma,
hepatic metastases,
peri-lesional steatosis,
#3748
Association of MINEN with GIST on neurofibromatosis – A case report
Introduction:
Although most digestive neuroendocrine tumors (NETs) are sporadic, around 5% of NETs occur in a context of hereditary predisposition, mainly type 1 multiple endocrine neoplasia (NEM1) and Von Hippel-Lindau disease (VHL).
Conference:
Presenting Author:
Authors:
Samia K,
Fatima H,
Nabil B,
Benali T,
Aisha B,
Keywords:
NEN,
GIST,
MINEN,
DOG1,
