S5024 When Crohn’s Climbs Higher: Esophageal Crohn's Disease

Introduction: Crohn's disease (CD) is a transmural inflammatory process that can affect any segment of the gastrointestinal tract. It mainly affects the small bowel, specifically the terminal ileum. Rarely, it has also been found in the upper gastrointestinal segment, such as the esophagus. In this case report, we describe a case of esophageal Crohn’s disease. Case Description/Methods: A 17-year-old man patient presented with a high fever, 2 episodes of hematemesis, heartburn, odynophagia, and dysphagia. He had these concerns for 3 days. He had no history of any other medical condition or drug abuse. His parents describe a history of Kawasaki disease in childhood. Laboratory results show elevated C-reactive protein levels, ferritin, and alpha1 and alpha2 globulins. Hepatitis B, C, cytomegalovirus, Epstein-Barr syndrome, and HIV 162 were negative. Ig E levels were normal. Upper endoscopy revealed esophageal ulcers, “bamboo-joint-like junctions” at the esophagus's middle and lower part, and partial duodenal bulb stenosis. The stomach was unremarkable. Ileo-colonoscopy showed no macroscopic findings. Biopsies were taken from ulcerated lesions in the esophagus. Histology revealed epithelial denudation, accompanied by diffuse, moderate to dense inflammatory infiltrates of lymphocytes, plasma cells, neutrophils, and numerous scattered macrophages. There was evidence of inflammatory granulation tissue with focal necrosis and 1 granuloma. Periodic acid–Schiff staining showed no evidence of fungal elements, ruling out mycotic involvement. Proton pump inhibitors and antifungals were administered initially. After the biopsy result, prednisolone and sucralfate were added, and the patient responded very well to corticosteroid therapy. Currently, the patient is on maintenance therapy with budesonide and proton pump inhibitors. Discussion: The diagnosis and treatment of esophageal CD is challenging. To our knowledge, we have not identified any reports of them in Albania. The workup to diagnose esophageal CD should include a clinical evaluation, baseline laboratory tests, endoscopic evaluation, histological assessment, and exclusion of other causes of esophagitis. Corticosteroids help manage acute inflammation; anti-tumor necrosis factor (anti-tumor necrosis factor) and immunomodulators remain the mainstay of therapy for esophageal Crohn's. In conclusion, clinicians should consider CD in atypical presentations of esophageal disease.

Authors

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001147556.92372.03
Primary Topic
Eosinophilic Esophagitis
Type
article
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article

S5024 When Crohn’s Climbs Higher: Esophageal Crohn's Disease

Qirjako Gjino, Fjona Tabaku, Denisa Horanlli, Suela Ristollari et al.
The American Journal of Gastroenterology
Eosinophilic Esophagitis
article

S5024 When Crohn’s Climbs Higher: Esophageal Crohn's Disease

Qirjako Gjino, Fjona Tabaku, Denisa Horanlli, Suela Ristollari, Aida Haxhillari
article en

Abstract

Introduction: Crohn's disease (CD) is a transmural inflammatory process that can affect any segment of the gastrointestinal tract. It mainly affects the small bowel, specifically the terminal ileum. Rarely, it has also been found in the upper gastrointestinal segment, such as the esophagus. In this case report, we describe a case of esophageal Crohn’s disease. Case Description/Methods: A 17-year-old man patient presented with a high fever, 2 episodes of hematemesis, heartburn, odynophagia, and dysphagia. He had these concerns for 3 days. He had no history of any other medical condition or drug abuse. His parents describe a history of Kawasaki disease in childhood. Laboratory results show elevated C-reactive protein levels, ferritin, and alpha1 and alpha2 globulins. Hepatitis B, C, cytomegalovirus, Epstein-Barr syndrome, and HIV 162 were negative. Ig E levels were normal. Upper endoscopy revealed esophageal ulcers, “bamboo-joint-like junctions” at the esophagus's middle and lower part, and partial duodenal bulb stenosis. The stomach was unremarkable. Ileo-colonoscopy showed no macroscopic findings. Biopsies were taken from ulcerated lesions in the esophagus. Histology revealed epithelial denudation, accompanied by diffuse, moderate to dense inflammatory infiltrates of lymphocytes, plasma cells, neutrophils, and numerous scattered macrophages. There was evidence of inflammatory granulation tissue with focal necrosis and 1 granuloma. Periodic acid–Schiff staining showed no evidence of fungal elements, ruling out mycotic involvement. Proton pump inhibitors and antifungals were administered initially. After the biopsy result, prednisolone and sucralfate were added, and the patient responded very well to corticosteroid therapy. Currently, the patient is on maintenance therapy with budesonide and proton pump inhibitors. Discussion: The diagnosis and treatment of esophageal CD is challenging. To our knowledge, we have not identified any reports of them in Albania. The workup to diagnose esophageal CD should include a clinical evaluation, baseline laboratory tests, endoscopic evaluation, histological assessment, and exclusion of other causes of esophagitis. Corticosteroids help manage acute inflammation; anti-tumor necrosis factor (anti-tumor necrosis factor) and immunomodulators remain the mainstay of therapy for esophageal Crohn's. In conclusion, clinicians should consider CD in atypical presentations of esophageal disease.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 41%
Eosinophilic Esophagitis
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