ReviewClinical journal of gastroenterology2015
Clinicopathologic features of chronic nonspecific multiple ulcers of the small intestine.
Review in Clinical journal of gastroenterology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.
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Who cites it
21 citing papers in PubMed, 31 citations in OpenAlex.
- BiallelicFrontiers in endocrinology · 2026Article
- A pediatric patient with chronic enteropathy associated with SLCO2A1 who underwent multimodal treatment including several surgeries: a case report.Frontiers in surgery · 2025Article
- Indolent T-cell Lymphoproliferative Disorder of the Gastrointestinal Tract Mimicking Crohn's Disease.Cureus · 2024Article
- First case report of dichorionic diamniotic twins with chronic enteropathy associated with the SLCO2A1 gene.Clinical journal of gastroenterology · 2024Article
- A rare case of bleeding jejunal ulcer diagnosed by intraoperative use of enteroscopy.International journal of surgery case reports · 2024Article
- A Novel Chronic Enteropathy Associated withKorean journal of radiology · 2023Article
- Clinical and Genetic Characteristics of Korean Patients Diagnosed with Chronic Enteropathy Associated withGut and liver · 2022Article
- Chronic Enteropathy Associated with Solute Carrier Organic Anion Transporter Family, Member 2A1 (SLCO2A1) with Positive Immunohistochemistry for SLCO2A1 Protein.Internal medicine (Tokyo, Japan) · 2022Article
- Four Variants of SLCO2A1 Identified in Three Chinese Patients with Chronic Enteropathy Associated with the SLCO2A1 Gene.Digestive diseases and sciences · 2021Article
- A case report of intestinal obstruction caused by cryptogenic multifocal ulcerous stenosing enteritis.BMC gastroenterology · 2020Article
- Fatal course of idiopathic chronic ulcerative enteritis with panenteritis and perforation: a case report and review of literature.BMC surgery · 2020Review
- Chronic Enteropathy Associated with SLCO2A1 with Pachydermoperiostosis.Internal medicine (Tokyo, Japan) · 2020Article
- Cryptogenic Multifocal Ulcerating Stenosing Enteropathy(CMUSE) and/or Chronic Non-specific Multiple Ulcers of the Small Intestine(CNSU) and Non-granulomatous Ulcerating Jejunoileitis (NGUJI).Current gastroenterology reports · 2019Review
- Measurement of prostaglandin metabolites is useful in diagnosis of small bowel ulcerations.World journal of gastroenterology · 2019Observational
- Distinction between Chronic Enteropathy Associated with theGut and liver · 2019Article
- Clinical features of chronic enteropathy associated with SLCO2A1 gene: a new entity clinically distinct from Crohn's disease.Journal of gastroenterology · 2018Article
- Genetic analysis is helpful for the diagnosis of small bowel ulceration.World journal of gastroenterology · 2018Article
- Immunohistochemical differentiation between chronic enteropathy associated withIntestinal research · 2018Article
- A rare cause of multiple small bowel ulcers and strictures in a 10-year-old child.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2018Article
- Roles of Organic Anion Transporting Polypeptide 2A1 (OATP2A1/SLCO2A1) in Regulating the Pathophysiological Actions of Prostaglandins.The AAPS journal · 2017Review
Corrections and comments
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Chronic nonspecific multiple ulcers of the small intestine is a rare but distinct clinical condition, characterized by multiple small intestinal ulcers of nonspecific histology and chronic, persistent gastrointestinal bleeding without nonsteroidal anti-inflammatory drug use. However, because of the term "nonspecific" in its nomenclature, some gastroenterologists have misinterpreted the disease as the condition with small intestinal ulcers caused by undetermined etiologies without considering clinical features. Such misinterpretation has led to the heterogeneity of clinicopathologic features of the disease, as well as to ambiguity regarding a possible genetic contribution. It thus seems necessary to recognize the clinical entity of the disease precisely to avoid misinterpretation. In this review, we describe the clinicopathologic features, differential diagnosis, and the possibility of a genetic contribution to the disease.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.