Purpose Neuroendocrine neoplasms can occur as part of inherited disorders, usually in the
form of well-differentiated, slow-growing tumors (NET). The main predisposing syndromes …

Insulinoma and glucagonoma are two rare functioning neoplasms of the neuroendocrine
cells of the pancreas, respectively, characterized by an uncontrolled over-secretion of insulin …

Differential diagnosis of hypoglycemia in the non-diabetic adult patient is complex and
comprises various diseases, including endogenous hyperinsulinism caused by functional β …

Mahvash disease in Pancreas in 2008. 1 In the last 10 years, more than 10 cases of
Mahvash disease, including 3 in a family, have been identified, a murine model established …

Objective: Rare co-existance of disease or pathology Background: Nesidioblastosis is a rare
disease that is part of the differential diagnosis of pancreatogenic hyperinsulinemic …

Mahvash disease is a rare autosomal recessive hereditary pancreatic neuroendocrine tumor
syndrome characterized by inactivating mutations in the glucagon receptor …

Differential diagnosis of hypoglycemia in the non-diabetic adult patient is complex and
comprises various diseases, including endogenous hyperinsulinism caused by functional β …

Discussion: The pathophysiology of nesidioblastosis is unknown, its main differential
diagnosis is insulinoma and this should be suspected when the tumor can not be identified …

Cadmium is a soft silvery-white metal, one of the 126 priority pollutants, and is also classified
in the group of category I human carcinogens. The aim of the study is the …

Pancreatic neuroendocrine tumors (PanNETs) are relatively uncommon, accounting for
approximately 2% of all pancreatic neoplasms. They occur in a younger age group than …