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Fabry disease presenting with sudden hearing loss and otosclerosis: a case report
INTRODUCTION: Fabry disease is an X-linked lysosomal storage disorder resulting in a multiple-system disorder with a wide spectrum of physical signs and symptoms, predominantly affecting the central and peripheral nervous systems, skin, heart, kidneys, and eyes. CASE PRESENTATION: We describe the ca...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342865/ https://www.ncbi.nlm.nih.gov/pubmed/22507244 http://dx.doi.org/10.1186/1752-1947-6-112 |
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author | Felisati, Giovanni Salvatici, Elisabetta Pipolo, Carlotta Portaleone, Sara Riva, Enrica Giovannini, Marcello |
author_facet | Felisati, Giovanni Salvatici, Elisabetta Pipolo, Carlotta Portaleone, Sara Riva, Enrica Giovannini, Marcello |
author_sort | Felisati, Giovanni |
collection | PubMed |
description | INTRODUCTION: Fabry disease is an X-linked lysosomal storage disorder resulting in a multiple-system disorder with a wide spectrum of physical signs and symptoms, predominantly affecting the central and peripheral nervous systems, skin, heart, kidneys, and eyes. CASE PRESENTATION: We describe the case of a 26-year-old European Caucasian man who had Fabry disease and who presented with episodic sudden unilateral hearing loss and was treated with glucocorticoids, pentoxifylline, hyperbaric oxygen, and fluoride because of concomitant audiometric evidence of otosclerosis. This case demonstrates the partial and transient beneficial effect of standard treatment for sudden hearing loss not related to Fabry disease and analyzes the possible connection between typical Fabry disease inner-ear lesions and otosclerosis. Whereas hearing loss has been described in connection with Fabry disease, otosclerosis-associated hearing loss in Fabry disease has not yet been described. CONCLUSIONS: Although progressive hearing loss in patients with Fabry disease seems to be influenced by replacement therapy, few data concerning treatment of sudden hearing loss are available. The lack of literature concerning the pathogenesis of the otological involvement in Fabry disease makes it impossible to identify a connection between the latter and otosclerosis. Therefore, this report may help to reinforce the importance of a thorough evaluation of hearing in patients with Fabry disease and may be of help with therapeutic decision-making. |
format | Online Article Text |
id | pubmed-3342865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33428652012-05-04 Fabry disease presenting with sudden hearing loss and otosclerosis: a case report Felisati, Giovanni Salvatici, Elisabetta Pipolo, Carlotta Portaleone, Sara Riva, Enrica Giovannini, Marcello J Med Case Reports Case Report INTRODUCTION: Fabry disease is an X-linked lysosomal storage disorder resulting in a multiple-system disorder with a wide spectrum of physical signs and symptoms, predominantly affecting the central and peripheral nervous systems, skin, heart, kidneys, and eyes. CASE PRESENTATION: We describe the case of a 26-year-old European Caucasian man who had Fabry disease and who presented with episodic sudden unilateral hearing loss and was treated with glucocorticoids, pentoxifylline, hyperbaric oxygen, and fluoride because of concomitant audiometric evidence of otosclerosis. This case demonstrates the partial and transient beneficial effect of standard treatment for sudden hearing loss not related to Fabry disease and analyzes the possible connection between typical Fabry disease inner-ear lesions and otosclerosis. Whereas hearing loss has been described in connection with Fabry disease, otosclerosis-associated hearing loss in Fabry disease has not yet been described. CONCLUSIONS: Although progressive hearing loss in patients with Fabry disease seems to be influenced by replacement therapy, few data concerning treatment of sudden hearing loss are available. The lack of literature concerning the pathogenesis of the otological involvement in Fabry disease makes it impossible to identify a connection between the latter and otosclerosis. Therefore, this report may help to reinforce the importance of a thorough evaluation of hearing in patients with Fabry disease and may be of help with therapeutic decision-making. BioMed Central 2012-04-16 /pmc/articles/PMC3342865/ /pubmed/22507244 http://dx.doi.org/10.1186/1752-1947-6-112 Text en Copyright ©2012 Felisati et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Felisati, Giovanni Salvatici, Elisabetta Pipolo, Carlotta Portaleone, Sara Riva, Enrica Giovannini, Marcello Fabry disease presenting with sudden hearing loss and otosclerosis: a case report |
title | Fabry disease presenting with sudden hearing loss and otosclerosis: a case report |
title_full | Fabry disease presenting with sudden hearing loss and otosclerosis: a case report |
title_fullStr | Fabry disease presenting with sudden hearing loss and otosclerosis: a case report |
title_full_unstemmed | Fabry disease presenting with sudden hearing loss and otosclerosis: a case report |
title_short | Fabry disease presenting with sudden hearing loss and otosclerosis: a case report |
title_sort | fabry disease presenting with sudden hearing loss and otosclerosis: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342865/ https://www.ncbi.nlm.nih.gov/pubmed/22507244 http://dx.doi.org/10.1186/1752-1947-6-112 |
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