Results 81 to 90 of about 15,083 (188)
Journal of Diabetes Investigation, Volume 17, Issue 8, Page 1254-1256, August 2026.
Nozomi Kido, Shun‐ichiro Asahara
wiley +1 more source
Insulinoma; a diagnostic challenge: a case report
Insulinoma is a pancreatic neuroendocrine tumour that primarily leads to episodes of hypoglycaemia due to inappropriate and excessive secretion of insulin.
Wania Rafaey +4 more
doaj +1 more source
Introduction: Endogenous hyperinsulinaemic hypoglycaemia (EHH) is characterized by inappropriate insulin secretion from pancreatic beta cells despite low blood glucose concentrations.
Setu Gupta +7 more
doaj +1 more source
CLINICAL CASE OF DIFFERENTIAL DIAGNOSIS OF HYPOGLYCEMIA SYNDROME
The article presents a clinical case of insulinoma, which is the most common, hormone-producing tumor of the pancreas, manifested by hyperinsulinemic hypoglycemia. The prevalence of insulinoma in the general population is estimated to be about
Елизавета Эдуардовна Епифанова +4 more
doaj
Low sensitivity of chromogranin A in the diagnosis of insulinoma: a single-center study
Background: Insulinoma is a neuroendocrine tumor (NET), with its main clinical manifestation being the hypoglycemic syndrome. The symptoms of hypoglycemia are nonspecific, and therefore, in most cases, the diagnosis is made untimely. The Russian clinical
Marina Y. Yukina +5 more
doaj +1 more source
Background. Insulinoma is one of the causes of recurrent hypoglycemia, one of the chief complaints for emergency department admission. The gold standard in diagnosing insulinoma is a 72-hour fasting test which is inconvenient and inefficient as it ...
Fransiskus Mikael Chandra +1 more
doaj +1 more source
Introduction: Insulinoma during pregnancy is a rare condition with vague clinical symptoms, making diagnosis challenging. The standard treatment for insulinoma is surgical tumor removal, preferably using a minimally invasive method.
Voraboot Taweerutchana +5 more
doaj +1 more source
Rare disease. Insulinomas are pancreatic neuroendocrine tumors that cause non-ketotic hypoglycemia due to hyperinsulinism; they are extremely rare, especially in children. We present a case of a sporadic insulinoma in an 11-year-old boy who had episodes of self-limited drowsiness and behavior changes over a 3-month period, thought to be caused by ...
Escartín, Rocío|| +4 more
+6 more sources

