Surufatinib related nephrotic syndrome in a pancreatic neuroendocrine tumor: a case report and review of literature
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Pancreatic neuroendocrine tumors (pNETs) are rare, heterogenous neoplasms originating from pancreatic neuroendocrine cells, which regulate hormone secretion and metabolic homeostasis. Surgery is the primary method of control and potential cure for pNETs and ta... ...
