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Copyright: ©Author(s) 2026. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution-NonCommercial (CC BY-NC 4.0) license. No commercial re-use. See permissions. Published by Baishideng Publishing Group Inc.
World J Gastroenterol. Apr 28, 2026; 32(16): 117236
Published online Apr 28, 2026. doi: 10.3748/wjg.v32.i16.117236
Silent progression and therapeutic reversibility of pediatric hepatitis B virus-related cirrhosis: Needs unmet
Larry Huang, Jialing Huang
Larry Huang, University of Pennsylvania, Philadelphia, PA 19104, United States
Jialing Huang, Department of Pathology, Geisinger Medical Center, Geisinger Commonwealth School of Medicine, Danville, PA 17822, United States
Co-first authors: Larry Huang and Jialing Huang.
Author contributions: Huang J collected data and revised the manuscript; Huang L collected and analyzed the data and wrote the manuscript.
Conflict-of-interest statement: All the authors report no relevant conflicts of interest for this article.
Corresponding author: Jialing Huang, MD, PhD, Associate Professor, Department of Pathology, Geisinger Medical Center, Geisinger Commonwealth School of Medicine, 100 N Academy Avenue, Danville, PA 17822, United States. jhuang1@geisinger.edu
Received: December 2, 2025
Revised: December 31, 2025
Accepted: February 25, 2026
Published online: April 28, 2026
Processing time: 136 Days and 11 Hours
Core Tip

Core Tip: This editorial emphasizes that pediatric hepatitis B virus-related cirrhosis is a silent yet rapidly progressive condition that is often overlooked, despite its potential reversibility with timely antiviral therapy. Unlike adult cirrhosis, pediatric cases frequently present without symptoms, making early detection through routine screening essential. The manuscript highlights the unique pathophysiology in children: Marked high viral replication, minimal inflammation, and strong regenerative capacity, which creates a critical therapeutic window for fibrosis regression and functional cure. We recommend structured pediatric programs emphasizing periodic virologic and biochemical testing, a low threshold for elastography and other noninvasive fibrosis tools, prompt initiation of antiviral therapy in high-risk children, and sustained adherence support. These measures, coupled with reinforced perinatal prevention, can materially improve long-term outcomes.