| Literature DB >> 23228815 |
Silvia Goñi Esarte1, Antonio Arín Letamendía, Juan José Vila Costas, Francisco Javier Jiménez Pérez, David Ruiz-Clavijo García, Juan Carrascosa Gil, María Luz Almendral López.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2012 PMID: 23228815 DOI: 10.1016/j.gastrohep.2012.07.004
Source DB: PubMed Journal: Gastroenterol Hepatol ISSN: 0210-5705 Impact factor: 2.102