Clinical and morphogenetic features of renal neuroendocrine tumors
#3686
Introduction: Renal neuroendocrine tumors (RenNETs) are extremely rare.
Aim(s): The aim of this study is to characterize a series of RenNETs in terms of their clinical, histopathological, immunohistochemical, and genetical features.
Materials and methods: Surgical samples of RenNETs from 13 patients were classified according to the 2022 WHO classification of endocrine tumors. The genomic profile was studied using a next generation sequencing (NGS) assay.
Conference:
Presenting Author: Kasajima A
Authors: Kasajima A, Pfarr N, von Werder A, Schwamborn K, Esposito I,
Keywords: Renal NET, WHO classification, Histology, immunohistochemistry, NGS,
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