Rituximab as rescue therapy in refractory esophageal lichen planus

Esophageal lichen planus (ELP) is a rare condition with unknown prevalence that can sometimes be underestimated due to the subtle and nonspecific findings of diagnostic workup. Oral lesions rarely extend to the esophageal mucosa, but when they do, the most frequent symptoms are dysphagia and odynoph...

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Published inGastroenterología y hepatología Vol. 36; no. 4; p. 264
Main Authors Goñi Esarte, Silvia, Arín Letamendía, Antonio, Vila Costas, Juan José, Jiménez Pérez, Francisco Javier, Ruiz-Clavijo García, David, Carrascosa Gil, Juan, Almendral López, María Luz
Format Journal Article
LanguageSpanish
Published Spain 01.04.2013
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Summary:Esophageal lichen planus (ELP) is a rare condition with unknown prevalence that can sometimes be underestimated due to the subtle and nonspecific findings of diagnostic workup. Oral lesions rarely extend to the esophageal mucosa, but when they do, the most frequent symptoms are dysphagia and odynophagia. There is often a significant delay in diagnosis and inadequate treatment. We report the case of a 59-year-old woman diagnosed with ELP, successfully treated with rituximab, a chimeric monoclonal antibody that depletes CD20+B cells. To our knowledge, this is only the second report of this treatment in ELP.
ISSN:0210-5705
DOI:10.1016/j.gastrohep.2012.07.004