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Insulinomais a rare tumor of the pancreasbelonging to the group of functional neuroendocrine tumors, and isitsmostcommonform. It affects 1 to 4 individuals per 1 million of the general population. Neuroglycopenic manifestations are the most dominant, makingdiagnosisoftenlate, which has benefitedfrom the development of variousmorphologicalmeans of exploration. The management of thesetumorsincludes conservative treatment of hypoglycemiainduced by insulinhypersecretion, non-invasive procedures and

Author

IJAR JOURNAL

Language

EN