Surufatinib related nephrotic syndrome in a pancreatic neuroendocrine tumor: a case report and review of literature

Surufatinib related nephrotic syndrome in a pancreatic neuroendocrine tumor: a case report and review of literature

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 targeted therapies have also been investig...

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Bibliographic Details
Main Authors: Chengqian Shi, Jinglian Lin, Xiadan Xiang, Wenlong Bao, Jie Yang
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-05-01
Series:Frontiers in Oncology
Subjects:
pancreatic neuroendocrine tumors
IgA nephropathy
nephrotic syndrome
surufatinib
podocyte
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2025.1546217/full
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