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Published in: Orphanet Journal of Rare Diseases 1/2010

Open Access 01-12-2010 | Case Report

Rituximab ameliorated severe hearing loss in Cogan's syndrome: a case report

Authors: Jelka G Orsoni, Bruno Laganà, Pierangela Rubino, Laura Zavota, Salvatore Bacciu, Paolo Mora

Published in: Orphanet Journal of Rare Diseases | Issue 1/2010

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Abstract

Background

Rituximab is a monoclonal antibody inducing depletion of B lymphocytes and presently approved for the treatment of non-Hodgkin's lymphoma and rheumatoid arthritis. Here is the first report of the use of this drug in a case of Cogan's syndrome (CS).

Case Presentation

a 25-year-old Italian woman was referred with conjunctival hyperaemia, interstitial keratitis, moderate bilateral sensorineural hearing loss accompanied by tinnitus, dizziness, nausea and vertigo, poorly responsive to oral and topical steroidal therapy. Diagnosis of typical CS was made. The administration of a combined immunosuppressive treatment resolved ocular inflammation, dizziness, nausea, and vertigo but gave little results in controlling progressive hearing loss. A noticeable improvement in hearing function was documented by pure tone audiometry after infusion of Rituximab.

Discussion

in CS, hearing function is often the most difficult parameter to control with therapy. A positive effect of Rituximab on was observed in our case. The drug also allowed to significantly reduce the number of adjuvant immunosuppressive medications.
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Metadata
Title
Rituximab ameliorated severe hearing loss in Cogan's syndrome: a case report
Authors
Jelka G Orsoni
Bruno Laganà
Pierangela Rubino
Laura Zavota
Salvatore Bacciu
Paolo Mora
Publication date
01-12-2010
Publisher
BioMed Central
Published in
Orphanet Journal of Rare Diseases / Issue 1/2010
Electronic ISSN: 1750-1172
DOI
https://doi.org/10.1186/1750-1172-5-18

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