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Sclerosing Esophagitis with IgG4-positive Plasma Cell Infiltration
Shigeo Mori1, Yoshiya Tahashi1, Kazushige Uchida1
1Third Department of Internal Medicine, Kansai Medical University, Japan.
This case report details a rare instance of IgG4-related disease manifesting solely as esophageal lesions. The condition caused progressive difficulty swallowing and esophageal strictures in a 76-year-old woman.
Area of Science:
- Gastroenterology
- Immunology
- Pathology
Background:
- Immunoglobulin G4-related disease (IgG4-RD) is a chronic fibroinflammatory condition that can affect various organs.
- Esophageal involvement in IgG4-RD is uncommon, with most reported cases involving other concurrent organ manifestations.
Observation:
- A 76-year-old woman presented with a 3-year history of progressive dysphagia, which worsened after cervical cancer surgery.
- Endoscopic and imaging studies revealed circumferential esophageal erosion and a thoracic esophageal stricture.
- Histological examination of the resected esophagus showed transmural hyperplasia with abundant IgG4-positive plasma cells and lymphocytes.
Findings:
- The patient was diagnosed with probable IgG4-related disease based on the esophageal findings.
- The esophageal lesions, including stricture and wall thickening, were characterized by inflammatory granulation tissue rich in IgG4-positive plasma cells.
Implications:
- This case highlights the importance of considering IgG4-related disease in the differential diagnosis of esophageal strictures, even in the absence of other organ involvement.
- Recognizing IgG4-related esophageal disease is crucial for appropriate diagnosis and management, potentially preventing complications associated with untreated esophageal strictures.
- Further research is needed to understand the specific mechanisms and prevalence of IgG4-related disease presenting exclusively in the esophagus.
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