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Plummer-Vinson Syndrome in an African-American Woman
Plummer-Vinson syndrome (PVS) presents with the classic triad of iron-deficiency anemia, dysphagia, and esophageal webs. The mainstay treatment of PVS is iron supplementation and the dysphagia usually responds to iron supplementation before the hematologic abnormalities are corrected. This syndrome...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8454221/ https://www.ncbi.nlm.nih.gov/pubmed/34616256 http://dx.doi.org/10.1159/000516937 |
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author | Patel, Keshav Kassir, Mahmoud Patel, Madhav Eichorn, Wesley |
author_facet | Patel, Keshav Kassir, Mahmoud Patel, Madhav Eichorn, Wesley |
author_sort | Patel, Keshav |
collection | PubMed |
description | Plummer-Vinson syndrome (PVS) presents with the classic triad of iron-deficiency anemia, dysphagia, and esophageal webs. The mainstay treatment of PVS is iron supplementation and the dysphagia usually responds to iron supplementation before the hematologic abnormalities are corrected. This syndrome classically affects middle-aged Caucasian women and very few cases have been reported in African Americans. We present a rare case of PVS in an African-American woman. A 63-year-old woman presented with shortness of breath, dysphagia, and lightheadedness for several weeks. Chest X-ray was negative for any acute abnormalities. Initial hemoglobin was 7.0 g/dL, which improved to 7.5 g/dL after 1 unit of packed red blood cells. She had a mean corpuscular volume of 62 fL, a ferritin level of 6 ng/mL, and an iron level of 12 μg/dL. Fecal occult blood test was negative and barium swallow revealed a proximal esophageal web. Her dysphagia did not significantly improve despite intravenous iron supplementation and esophageal web dilation. Video-fluoroscopic swallow study revealed esophageal and pharyngeal phase dysphagia with food entrapment. She was discharged with plans to follow up with a primary care physician and repeat esophagogastroduodenoscopy in 1 year. This case report highlights a rare case of PVS in an African-American woman and emphasizes the importance of maintaining a comprehensive and broad differential diagnosis. |
format | Online Article Text |
id | pubmed-8454221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-84542212021-10-05 Plummer-Vinson Syndrome in an African-American Woman Patel, Keshav Kassir, Mahmoud Patel, Madhav Eichorn, Wesley Case Rep Gastroenterol Single Case Plummer-Vinson syndrome (PVS) presents with the classic triad of iron-deficiency anemia, dysphagia, and esophageal webs. The mainstay treatment of PVS is iron supplementation and the dysphagia usually responds to iron supplementation before the hematologic abnormalities are corrected. This syndrome classically affects middle-aged Caucasian women and very few cases have been reported in African Americans. We present a rare case of PVS in an African-American woman. A 63-year-old woman presented with shortness of breath, dysphagia, and lightheadedness for several weeks. Chest X-ray was negative for any acute abnormalities. Initial hemoglobin was 7.0 g/dL, which improved to 7.5 g/dL after 1 unit of packed red blood cells. She had a mean corpuscular volume of 62 fL, a ferritin level of 6 ng/mL, and an iron level of 12 μg/dL. Fecal occult blood test was negative and barium swallow revealed a proximal esophageal web. Her dysphagia did not significantly improve despite intravenous iron supplementation and esophageal web dilation. Video-fluoroscopic swallow study revealed esophageal and pharyngeal phase dysphagia with food entrapment. She was discharged with plans to follow up with a primary care physician and repeat esophagogastroduodenoscopy in 1 year. This case report highlights a rare case of PVS in an African-American woman and emphasizes the importance of maintaining a comprehensive and broad differential diagnosis. S. Karger AG 2021-06-22 /pmc/articles/PMC8454221/ /pubmed/34616256 http://dx.doi.org/10.1159/000516937 Text en Copyright © 2021 by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission. |
spellingShingle | Single Case Patel, Keshav Kassir, Mahmoud Patel, Madhav Eichorn, Wesley Plummer-Vinson Syndrome in an African-American Woman |
title | Plummer-Vinson Syndrome in an African-American Woman |
title_full | Plummer-Vinson Syndrome in an African-American Woman |
title_fullStr | Plummer-Vinson Syndrome in an African-American Woman |
title_full_unstemmed | Plummer-Vinson Syndrome in an African-American Woman |
title_short | Plummer-Vinson Syndrome in an African-American Woman |
title_sort | plummer-vinson syndrome in an african-american woman |
topic | Single Case |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8454221/ https://www.ncbi.nlm.nih.gov/pubmed/34616256 http://dx.doi.org/10.1159/000516937 |
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