Korean J Med.  2004 Nov;67(Suppl 3):S703-S707.

A case of Plummer-Vinson syndrome treated with endoscopic bougienage

Affiliations
  • 1Institute for Digestive research, Department of Internal Medicine, Soonchunhyang University Medical College, Seoul, Korea. csshim@hosp.sch.ac.kr
  • 2Department of Radiology, Soonchunhyang University Medical College, Seoul, Korea.

Abstract

Plummer-Vinson syndrome comprises the triad of dysphagia, iron-deficiency anemia and postcricoid esophageal web. Its report in our country is very rare. A 39-year-old woman developed dysphagia and odynophagia progressively for 10 years from solid meal to a liquid. Endoscopy revealed a pink-colored membrane and a pin-point, eccentric opening present just below the upper esophageal sphincter. Esophagography with barium contrast revealed a thin, eccenteric, radiolucent bar across the esophagus on the level of thoracic inlet and partial obstruction is suggested by dilatation of the proximal portion of esophageal web. For relief of dysphagia, endoscopic bougienage was planned. After endoscopic bougienage, it was allowed passage of endoscope to distal esophagus and she felt good for swallowing of solids. Endoscopic bougienage should be considered in Plummer-Vinson syndrome with severe stenotic lesions whose clinical condition is worsening in spite of tranditional supportive care.

Keyword

Plummer-Vinson syndrome; Dilatation; Endoscopic

MeSH Terms

Adult
Anemia, Iron-Deficiency
Barium
Bays
Deglutition
Deglutition Disorders
Dilatation
Endoscopes
Endoscopy
Esophageal Sphincter, Upper
Esophagus
Female
Humans
Meals
Membranes
Plummer-Vinson Syndrome*
Barium
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