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©The Author(s) 2025. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Nephrol. Jun 25, 2025; 14(2): 99380
Published online Jun 25, 2025. doi: 10.5527/wjn.v14.i2.99380
Published online Jun 25, 2025. doi: 10.5527/wjn.v14.i2.99380
Paediatric renal tumors: An insight into molecular characteristics, histomorphology and syndromic association
Mousmi Agrawal, Amit K Chowhan, Department of Pathology and Lab Medicine, All India Institute of Medical Sciences (AIIMS), Raipur 492099, Chhattisgarh, India
Author contributions: Agrawal M contributed to material preparation, first draft of manuscript and literature search; Chowhan AK contributed to literature search and editing of manuscript.
Conflict-of-interest statement: All the authors report no relevant conflicts of interest for this article.
Open Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Amit K Chowhan, MD, Professor, Department of Pathology and Lab Medicine, All India Institute of Medical Sciences (AIIMS), Raipur 492099, Chhattisgarh, India. chowhanpath@aiimsraipur.edu.in
Received: July 21, 2024
Revised: December 19, 2024
Accepted: January 14, 2025
Published online: June 25, 2025
Processing time: 262 Days and 3.7 Hours
Revised: December 19, 2024
Accepted: January 14, 2025
Published online: June 25, 2025
Processing time: 262 Days and 3.7 Hours
Core Tip
Core Tip: This article outlines about paediatric renal tumors. They can have asymptomatic to symptomatic presentation. Every tumor has its own unique histomorphology, immunohistochemistry and molecular pathology. Certain tumors have association with genetic syndromes, which makes it prognostically more challenging for children. Knowledge and awareness of these tumors are essential for their accurate diagnosis and early treatment.