Chronic Enteropathy Associated With SLCO2A1 Gene Mutation; Initially Misdiagnosed as Fibrostenosing Crohn's Disease

ABSTRACT Chronic enteropathy associated with SLCO2A1 (CEAS) is a rare condition that can mimic fibrostenosing Crohn's disease. We describe a young man with presumed Crohn's disease marked by recurrent bowel obstruction, multiple surgical resections, and poor response to standard therapies, with histopathology showing atypical findings. He developed systemic manifestations of CEAS, including pachydermoperiostosis (digital clubbing, periosteal new bone formation, and skin thickening) and hypertrophic osteoarthropathy. Subsequent genetic testing identified a pathogenic SLCO2A1 mutation. Treatment with COX-2 and PDE-4 inhibitors, combined with conventional therapy, reduced disease activity, underscoring the importance of recognizing atypical features and early genetic testing.

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Publication Details

Journal
ACG Case Reports Journal
Published
2026-10-30
DOI
https://doi.org/10.14309/crj.0000000000002388
Primary Topic
Inflammatory Bowel Disease
Type
article
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article

Chronic Enteropathy Associated With SLCO2A1 Gene Mutation; Initially Misdiagnosed as Fibrostenosing Crohn's Disease

Heba N. Iskandar, Prateek C. Gandiga, Hayalneh Gessessew, David Qin et al.
2 links
ACG Case Reports Journal
Inflammatory Bowel Disease
article

Chronic Enteropathy Associated With SLCO2A1 Gene Mutation; Initially Misdiagnosed as Fibrostenosing Crohn's Disease

Heba N. Iskandar, Prateek C. Gandiga, Hayalneh Gessessew, David Qin, Navila Sharif
article en

Abstract

ABSTRACT Chronic enteropathy associated with SLCO2A1 (CEAS) is a rare condition that can mimic fibrostenosing Crohn's disease. We describe a young man with presumed Crohn's disease marked by recurrent bowel obstruction, multiple surgical resections, and poor response to standard therapies, with histopathology showing atypical findings. He developed systemic manifestations of CEAS, including pachydermoperiostosis (digital clubbing, periosteal new bone formation, and skin thickening) and hypertrophic osteoarthropathy. Subsequent genetic testing identified a pathogenic SLCO2A1 mutation. Treatment with COX-2 and PDE-4 inhibitors, combined with conventional therapy, reduced disease activity, underscoring the importance of recognizing atypical features and early genetic testing.

ACG Case Reports JournalVol. 13(11)
Georgia Institute of Technology (US), Emory University (US), The Wallace H. Coulter Department of Biomedical Engineering (US), Vanderbilt University Medical Center (US)
Good health and well-being
Openalex Percentile: Top 15%
Inflammatory Bowel Disease
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Chronic Enteropathy Associated With SLCO2A1 Gene Mutation; Initially Misdiagnosed as Fibrostenosing Crohn's Disease — Heba N. Iskandar, Prateek C. Gandiga, et al. · ACG Case Reports Journal (2026) | TGRS Research Map | TGRS