2019
DOI: 10.2147/jmdh.s180410
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<p>Plummer-Vinson syndrome: improving outcomes with a multidisciplinary approach</p>

Abstract: Plummer-Vinson syndrome is a rare condition associated with dysphagia, iron deficiency, and esophageal webs. Data regarding this condition is limited to mostly case reports and a few small cohort studies. Although most cases have a benign and indolent course, the risk of malignancy warrants long-term surveillance. A multidisciplinary approach among healthcare providers is of the utmost importance in the management of this condition.

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Cited by 14 publications
(17 citation statements)
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“…It is often low-grade, intermittent, and painless. The progression of dysphagia is slow and can take several years [ 12 ]. Patients also often have IDA, which can present with non-specific signs and symptoms.…”
Section: Discussionmentioning
confidence: 99%
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“…It is often low-grade, intermittent, and painless. The progression of dysphagia is slow and can take several years [ 12 ]. Patients also often have IDA, which can present with non-specific signs and symptoms.…”
Section: Discussionmentioning
confidence: 99%
“…Autoimmunity is thought to play a role, as PVS is associated with other autoimmune conditions, such as celiac disease, rheumatoid arthritis, and Crohn’s disease. Furthermore, chronic inflammation from a variety of factors has been proposed as part of the pathogenesis [ 1 , 2 , 11 , 12 ]. H. pylori infection impairs iron absorption as a result of chronic gastritis, which causes gastric hypochlorhydria and subsequent impaired iron uptake and an increase in iron loss, potentially leading to IDA.…”
Section: Discussionmentioning
confidence: 99%
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