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RAPD 2026
VOL 49
N4 Julio - Agosto 2026
N4 July - August 2026

Datos de la publicación


Plummer-Vinson syndrome as an uncommon cause of progressive dysphagia


Abstract

Plummer–Vinson syndrome (PVS) is a very rare condition associated with iron-deficiency anemia and an increased risk of squamous cell carcinoma of the upper gastrointestinal tract.

We present the case of a 65-year-old woman with progressive dysphagia in whom endoscopic evaluation revealed cervical esophageal webs. Treatment with endoscopic dilation and iron supplementation led to clinical resolution.

This case highlights the importance of considering PVS in the differential diagnosis of dysphagia and of implementing targeted management with appropriate follow-up.

Keywords: Plummer-Vinson, esophageal web, dysphagia, anemia.


CORRESPONDENCE

Sixto Menacho Ordóñez

University Hospital of Jerez de la Frontera.

72000 Cádiz

sixmeor@gmail.com

CITE THIS WORK

Menacho Ordóñez S, García Martínez A, Marín Lara L. Plummer-Vinson syndrome as an uncommon cause of progressive dysphagia.RAPD 2026;49(4):142-143. DOI: 10.37352/2026494.4

Introduction

Plummer-Vinson syndrome is a very rare clinical condition defined by the triad of iron-deficiency anemia, dysphagia, and esophageal membranes, and its presentation has been described predominantly in middle-aged women1. Its pathophysiology is not fully understood, although it has been proposed that iron deficiency promotes epithelial atrophy and impairments in mucosal repair2.

Clinical case

A 65-year-old woman was referred for progressive dysphagia with solids that had been present for 12 months, associated with weight loss. The symptoms were initially attributed to poorly fitting dentures and possible oral candidiasis, but there was no improvement following treatment.

Physical examination revealed glossitis, angular cheilitis, and a depapillated tongue. Laboratory tests showed iron-deficiency anemia.

The esophagogram revealed a proximal esophageal membrane. Upper gastrointestinal endoscopy confirmed stenosis secondary to two cervical esophageal membranes without associated malignant lesions. Progressive endoscopic balloon dilation was performed (initially 7-;8 mm, increased to 10-12 mm in a second session) without complications, resulting in immediate symptomatic improvement. Treatment with oral iron was initiated, and laboratory values subsequently returned to normal.

Figure 1

Barium esophagram showing a proximal esophageal membrane with concentric narrowing of the lumen, a characteristic finding of Plummer-Vinson syndrome.

imagenes/cc2_fig1.jpg
Figure 2

Upper gastrointestinal endoscopy showing a cervical esophageal membrane with concentric narrowing of the lumen and a reduced central orifice, consistent with Plummer-Vinson syndrome.

imagenes/cc2_fig2.jpg

Discussion

PVS is currently a rare cause of dysphagia in developed countries1. Its diagnosis may be delayed because symptoms are initially attributed to more common causes. Recognition of mucocutaneous signs of iron deficiency can guide the diagnosis.

Iron supplementation forms the basis of treatment and can improve dysphagia in the early stages, whereas in cases with established stenosis, endoscopic dilation is safe and effective1,2. Despite its current low prevalence in developed countries, it remains clinically significant due to its association with squamous cell carcinoma of the hypopharynx and esophagus, underscoring the importance of early diagnosis and regular clinical follow-up3.

Bibliography

1 

Goel A, Bakshi SS, Soni N, et al. Iron deficiency anemia and Plummer-Vinson syndrome: current insights. J Blood Med 2017;8:175-84.

2 

Novacek G. Plummer-Vinson syndrome. Orphanet J Rare Dis. 2006;1:36

3 

Alzamzamy AE, Tag-Adeen M, Alyouzbaki AZ, Lashen SA, Ellakany WI, Okasha HH, et al. Plummer-Vinson syndrome: a retrospective multicenter study. Dig Dis Sci. 2025;70(10):3419–3424.