A Case of Plummer-Vinson Syndrome.
10.12701/yujm.1994.11.2.381
- Author:
Kyeong Jin JEON
;
Byeong Ik JANG
;
Tae Nyeun KIM
;
Moon Kwan CHUNG
;
Hyun Woo LEE
- Publication Type:Case Report
- MeSH:
Anemia;
Anemia, Iron-Deficiency;
Deglutition Disorders;
Dilatation;
Esophagus;
Female;
Glossitis;
Humans;
Iron;
Middle Aged;
Mouth;
Plummer-Vinson Syndrome*;
Skin Manifestations;
Tears
- From:Yeungnam University Journal of Medicine
1994;11(2):381-387
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Plummer-Vinson syndrome is a clinical entity characterized by dysphagia, iron deficiency anemia, cheilosis, glossitis, and cervical esophageal web, especially in middle aged women. Recently, the authors experienced a case of Plummer-Vinson syndrome. A 53-year-old female was admitted due to intermittent solid food dysphagia for 18 months. She had a 2 years history of iron deficiency anemia. On admission glossitis, fissures at the angle of the mouth, spoon nails, and iron deficiency anemia were noted. Esophagogram and esophagoscopic examination revealed thin walled concentric web at upper esophagus. Esophageal web was succefully teared by endoscopic balloon dilatation with subseguant improvement of dysphagia. Skin manifestations as well as anemia were markedly improved after oral iron replacement therapy.
