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Plummer-Vinson syndrome successfully treated by endoscopic dilatation
Masaru Enomoto1, Madoka Kohmoto, Usama Ahmed Arafa
1Third Department of Internal Medicine, Osaka City University Medical School, Abeno-ku, Osaka, Japan. enomoto-m@med.osaka-cu.ac.jp
Plummer-Vinson syndrome, characterized by iron deficiency anemia and esophageal webs, can cause severe dysphagia. Endoscopic bougienage effectively treated a patient
Area of Science:
- Gastroenterology
- Hematology
Background:
- Plummer-Vinson syndrome (Paterson-Brown-Kelly syndrome) is a rare condition characterized by iron deficiency anemia, esophageal webs, and dysphagia.
- While iron repletion is crucial, esophageal webs often necessitate mechanical intervention.
Observation:
- A 69-year-old woman presented with a history of anemia and progressive dysphagia to solids.
- Diagnostic imaging revealed iron deficiency anemia and two cervical esophageal webs causing a severe stricture.
Findings:
- Intravenous iron supplementation improved anemia but not dysphagia.
- Endoscopic bougienage using sequentially larger dilators successfully disrupted the esophageal webs without complications.
- The patient experienced complete resolution of dysphagia post-procedure.
Implications:
- Endoscopic bougienage is a safe and effective treatment for severe esophageal stenosis associated with Plummer-Vinson syndrome.
- This minimally invasive approach offers a viable solution when iron therapy alone is insufficient.
- The procedure demonstrates rapid symptom relief and long-term efficacy.
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