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Review
. 2025 Sep;60(9):1118-1144.
doi: 10.1007/s00535-025-02271-7. Epub 2025 Jul 2.

Expert consensus on diagnostic guidelines for pediatric inflammatory bowel disease in Japan

Affiliations
Review

Expert consensus on diagnostic guidelines for pediatric inflammatory bowel disease in Japan

Takahiro Kudo et al. J Gastroenterol. 2025 Sep.

Abstract

Background: Inflammatory bowel disease (IBD) can occur at any age. In pediatric patients, the disease may present with a broader range of symptoms and more severe course than in adults, due to ongoing growth and development. Therefore, pediatric IBD often exhibits an atypical clinical course and laboratory findings. It is essential to recognize differences in disease presentation, differential diagnoses, and evaluation strategies specific to children. The revised Porto criteria, proposed by the European Society for Paediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN) in 2014, are widely used globally, including in Japan, for the diagnosis of pediatric IBD.

Purpose: Despite the widespread use of these criteria, no formal diagnostic guidelines for pediatric IBD have been developed in Japan. We aimed to support future guideline development by summarizing important diagnostic considerations and clinical practices for pediatric IBD in Japan.

Methods: This review was developed based on relevant international diagnostic guidelines and the expert opinions of Japanese pediatric gastroenterologists. It outlines key clinical and laboratory evaluations, as well as current treatment and follow-up approaches.

Results: We summarized recommended diagnostic tests and clinical points that require special attention in children with suspected IBD. The article reflects both global standards and domestic clinical experience.

Conclusion: Although this article does not provide formal diagnostic criteria or assess evidence levels, it offers accurate and practical information to guide physicians and patients in the diagnosis and management of pediatric IBD in Japan.

Keywords: Children; Crohn’s disease; Inflammatory bowel disease; Pediatric; Ulcerative colitis.

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Conflict of interest statement

Declarations. Conflict of interest: Takashi Ishige received a consulting fee from AbbVie GK. Keisuke Jimbo received a grant Japan Society for the Promotion of Science KANENHI Grant-in-Aid for Scientific Research (c) [grant number 23K07361]. Fumihito Hirai received a consulting fee from AbbVie GK, EA pharma Co. Ltd., Janssen Pharmaceutical K.K., Mochida Pharmaceutical Co. Ltd., Mitsubishi Tanabe Pharma Corporation, Takeda Pharmaceutical Co. Ltd., Eli Lilly Japan K.K., MSD Co. Ltd., and a grant support from AbbVie GK, EA pharma Co. Ltd., Kyorin Pharmaceutical Co. Ltd., Mochida Pharmaceutical Co. Ltd.. Kenji Watanabe received a lecture fee from Takeda Pharmaceutical Co. Ltd., AbbVie GK, EA pharma Co. Ltd., Mitsubishi Tanabe Pharma Corporation, Mochida Pharmaceutical Co. Ltd., JIMRO Co. Ltd.. Toshiaki Shimizu received a research grant from The Food Science Institute Foundation (Ryoshoku-kenkyukai). Tadakazu Hisamatsu received a grant support from Mitsubishi Tanabe Pharma Corporation, EA pharma Co. Ltd., AbbVie GK, JIMRO Co. Ltd., Zeria Pharmaceutical Co. Ltd., Kyorin Pharmaceutical Co. Ltd., Nippon Kayaku Co. Ltd., Takeda Pharmaceutical Co. Ltd., Pfizer Inc., Mochida Pharmaceutical Co. Ltd., Boston Scientific Corporation, Kissei Pharmaceutical Co. Ltd., a consulting fee from Mitsubishi Tanabe Pharma Corporation, EA pharma Co. Ltd., AbbVie GK, Janssen Pharmaceutical K.K., Pfizer Inc., Eli Lilly, Gilead Sciences, Bristol Myers Squibb, Abivax, and a lecture fee from Mitsubishi Tanabe Pharma Corporation, AbbVie GK, EA pharma Co. Ltd., Kyorin Pharmaceutical Co. Ltd., JIMRO Co., Janssen Pharmaceutical K.K., Mochida Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co. Ltd., Pfizer Inc., Kissei Pharmaceutical Co. Ltd. All other authors declare no conflict of interest.

Figures

Fig. 1
Fig. 1
Diagnostic flowchart of pediatric inflammatory bowel disease (IBD) proposed by the European Society for Paediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN). Because of the risk of capsule retention in children, small bowel patency should be evaluated using a patency capsule before attempting small bowel capsule endoscopy (SBCE). BAE balloon enteroscopy, CD Crohn’s disease, IBD-U inflammatory bowel disease unclassified, MRE magnetic resonance enterography, UC ulcerative colitis
Fig. 2
Fig. 2
Algorithm of pediatric inflammatory bowel disease (IBD) classes used to determine the differential diagnosis of IBD subgroups. Adapted from [10], with partial modification. Upper row: number of applicable items among six features (no. 1–6 of class 1 of Table 4). Middle row: number of corresponding items among 12 features (no. 7–18 of class 2 of Table 4). Lower row: number of corresponding items among five features (no. 19–23 of class 3 of Table 4). CD Crohn’s disease, IBD-U inflammatory bowel disease unclassified, UC ulcerative colitis
Fig. 3
Fig. 3
Schematic diagram of clinical manifestations, pathological mechanisms, and therapeutic interventions associated with pediatric inflammatory bowel disease (IBD)-related stunted growth. Evidence for all pathways has not been fully established. Adapted from [10], with partial modification. GH growth hormone, IGF insulin-like growth factor, IL interleukin, QOL quality of life, TNF tumor necrosis factor

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