Editorial
Copyright ©The Author(s) 2024. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastrointest Oncol. Nov 15, 2024; 16(11): 4309-4314
Published online Nov 15, 2024. doi: 10.4251/wjgo.v16.i11.4309
Navigating the complex landscape of crawling-type gastric adenocarcinomas: Insights and implications for clinical practice
Hai-Bo Yu, Ke-Feng Jia, Xing-Fen Wang, Bao-Yu Li, Qi Xin
Hai-Bo Yu, Laboratory, The Second Hospital of Tianjin Medical University, Tianjin 300211, China
Ke-Feng Jia, Department of Radiology, Tianjin Third Central Hospital, Tianjin 300170, China
Xing-Fen Wang, Department of Pathology, The Second Hospital of Tianjin Medical University, Tianjin 300211, China
Bao-Yu Li, Department of Gastrointestinal Surgery, The Second Hospital of Tianjin Medical University, Tianjin 300211, China
Qi Xin, Department of Pathology, The Third Central Hospital of Tianjin, Tianjin 300170, China
Co-first authors: Hai-Bo Yu and Ke-Feng Jia.
Author contributions: Yu HB contributed to data collection; Wang XF evaluated the images; Xin Q contributed to the pathological analysis; Yu HB, Jia KF, and Li BY contributed to revision of the manuscript; All authors agreed to publication of the manuscript.
Supported by The Third Central Hospital of Tianjin, No. 2019YNR3.
Conflict-of-interest statement: The authors declare that they have no conflict of interest.
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: Qi Xin, PhD, Associate Chief Physician, Department of Pathology, The Third Central Hospital of Tianjin, No. 83 Jintang Road, Tianjin 300170, China. xinqi19820204@126.com
Received: March 18, 2024
Revised: June 3, 2024
Accepted: June 26, 2024
Published online: November 15, 2024
Processing time: 221 Days and 7.7 Hours
Abstract

In this editorial, we comment on an article by Xu et al. This article describes a case of crawling-type gastric adenocarcinoma (CRA) distinguished by its rare occurrence and diagnostic complexity. We reviewed the detailed case-report findings showcasing clinical, pathological, and molecular characteristics of CRA that shed light on its elusive nature and challenges for early detection and treatment. This case underscored the significance of advanced diagnostic tools such as endoscopic submucosal dissection. Emphasis was placed on the molecular peculiarities of CRA, including the higher mutation rates of genes such as TP53 and RHOA and the notable absence of HER2 amplification, differentiating it from more conventional forms of gastric adenocarcinoma. In this editorial, we advocate for a multidisciplinary approach to effectively manage this rare subtype and highlight the necessity for precision in both diagnostic and therapeutic strategies. Moreover, a heightened awareness urging the adoption of advanced diagnostic techniques and collaborative approaches is necessary among clinicians and researchers. We aim to contribute to the ongoing discourse in gastrointestinal oncology, emphasizing the importance of recognizing and addressing the complexities associated with rare cancer subtypes such as CRA.

Keywords: Crawling-type gastric adenocarcinoma; Diagnosis; Pathology; Endoscopy; Treatment

Core Tip: Crawling-type gastric adenocarcinoma (CRA) is characterized by its elusive presentation and propensity for lateral expansion within the mucosal layer, posing significant challenges to early detection. This study emphasizes the need for a multidisciplinary approach to achieve accurate diagnosis and effective treatment. The findings reveal distinct molecular features of CRA including the notably increased mutation frequencies in the TP53 and RHOA genes, and the absence of HER2 amplification. These characteristics highlight the critical need for precision in diagnostic and therapeutic modalities. The objective is to augment clinical awareness, thereby facilitating prompt identification and efficient management of this subtype of gastric cancer.