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Role of Handheld In Vivo Reflectance Confocal Microscopy for the Diagnosis of Fabry Disease: A Case Report

Fabry disease (FD) is a rare X-linked lysosomal storage disorder caused by the deficient activity of the lysosomal enzyme α-galactosidase that leads to a systemic accumulation of globotriaosylceramide. Handheld in vivo reflectance confocal microscopy (HH-RCM) is a useful modern technique in diagnosi...

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Autores principales: Cinotti, Elisa, Provvidenziale, Luca, Fimiani, Michele, Perrot, Jean Luc, Cambazard, Frederic, Rubegni, Pietro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6164009/
https://www.ncbi.nlm.nih.gov/pubmed/29954050
http://dx.doi.org/10.3390/diseases6030055
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author Cinotti, Elisa
Provvidenziale, Luca
Fimiani, Michele
Perrot, Jean Luc
Cambazard, Frederic
Rubegni, Pietro
author_facet Cinotti, Elisa
Provvidenziale, Luca
Fimiani, Michele
Perrot, Jean Luc
Cambazard, Frederic
Rubegni, Pietro
author_sort Cinotti, Elisa
collection PubMed
description Fabry disease (FD) is a rare X-linked lysosomal storage disorder caused by the deficient activity of the lysosomal enzyme α-galactosidase that leads to a systemic accumulation of globotriaosylceramide. Handheld in vivo reflectance confocal microscopy (HH-RCM) is a useful modern technique in diagnosis and follow-ups of many skin diseases. This noninvasive device provides high-resolution and high-contrast real-time images to study both the skin and the ocular surface structures that can help clinicians to confirm the diagnosis of FD. HH-RCM could be helpful even for the follow-ups of these patients, enabling us to monitor the effect of enzyme replacement therapy on corneal cells and keratinocytes.
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spelling pubmed-61640092018-10-11 Role of Handheld In Vivo Reflectance Confocal Microscopy for the Diagnosis of Fabry Disease: A Case Report Cinotti, Elisa Provvidenziale, Luca Fimiani, Michele Perrot, Jean Luc Cambazard, Frederic Rubegni, Pietro Diseases Case Report Fabry disease (FD) is a rare X-linked lysosomal storage disorder caused by the deficient activity of the lysosomal enzyme α-galactosidase that leads to a systemic accumulation of globotriaosylceramide. Handheld in vivo reflectance confocal microscopy (HH-RCM) is a useful modern technique in diagnosis and follow-ups of many skin diseases. This noninvasive device provides high-resolution and high-contrast real-time images to study both the skin and the ocular surface structures that can help clinicians to confirm the diagnosis of FD. HH-RCM could be helpful even for the follow-ups of these patients, enabling us to monitor the effect of enzyme replacement therapy on corneal cells and keratinocytes. MDPI 2018-06-27 /pmc/articles/PMC6164009/ /pubmed/29954050 http://dx.doi.org/10.3390/diseases6030055 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Cinotti, Elisa
Provvidenziale, Luca
Fimiani, Michele
Perrot, Jean Luc
Cambazard, Frederic
Rubegni, Pietro
Role of Handheld In Vivo Reflectance Confocal Microscopy for the Diagnosis of Fabry Disease: A Case Report
title Role of Handheld In Vivo Reflectance Confocal Microscopy for the Diagnosis of Fabry Disease: A Case Report
title_full Role of Handheld In Vivo Reflectance Confocal Microscopy for the Diagnosis of Fabry Disease: A Case Report
title_fullStr Role of Handheld In Vivo Reflectance Confocal Microscopy for the Diagnosis of Fabry Disease: A Case Report
title_full_unstemmed Role of Handheld In Vivo Reflectance Confocal Microscopy for the Diagnosis of Fabry Disease: A Case Report
title_short Role of Handheld In Vivo Reflectance Confocal Microscopy for the Diagnosis of Fabry Disease: A Case Report
title_sort role of handheld in vivo reflectance confocal microscopy for the diagnosis of fabry disease: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6164009/
https://www.ncbi.nlm.nih.gov/pubmed/29954050
http://dx.doi.org/10.3390/diseases6030055
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