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Autologous adipose-derived stromal vascular fraction and scarred vocal folds: first clinical case report

Patients with scarred vocal folds (congenitally or following phonosurgery) are currently difficult to treat and present a dysphonia, often disabling in daily life. Several therapies are available on the market but the results of these are often disappointing. The autologous adipose-derived stromal v...

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Autores principales: Mattei, Alexia, Magalon, Jérémy, Bertrand, Baptiste, Grimaud, Fanny, Revis, Joana, Velier, Mélanie, Veran, Julie, Dessi, Patrick, Sabatier, Florence, Giovanni, Antoine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6062967/
https://www.ncbi.nlm.nih.gov/pubmed/30053913
http://dx.doi.org/10.1186/s13287-018-0842-0
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author Mattei, Alexia
Magalon, Jérémy
Bertrand, Baptiste
Grimaud, Fanny
Revis, Joana
Velier, Mélanie
Veran, Julie
Dessi, Patrick
Sabatier, Florence
Giovanni, Antoine
author_facet Mattei, Alexia
Magalon, Jérémy
Bertrand, Baptiste
Grimaud, Fanny
Revis, Joana
Velier, Mélanie
Veran, Julie
Dessi, Patrick
Sabatier, Florence
Giovanni, Antoine
author_sort Mattei, Alexia
collection PubMed
description Patients with scarred vocal folds (congenitally or following phonosurgery) are currently difficult to treat and present a dysphonia, often disabling in daily life. Several therapies are available on the market but the results of these are often disappointing. The autologous adipose-derived stromal vascular fraction (ADSVF) is recognized as an easily accessible source of cells with angiogenic, anti-inflammatory, immunomodulatory, and regenerative properties. We present here the case of a 43-year-old woman who had a severe dysphonia associated with scarred vocal folds after a phonosurgery and was resistant to conventional medical and surgical treatments. She received a local administration of autologous ADSVF. The protocol involved, on the same day, adipose tissue extraction, ADSVF preparation, and then local injection (0.45ml of ADSVF in each vocal fold, for a total of 12.2 million ADSVF viable cells). No serious adverse events have been described. One year following the surgery, the laryngoscopic aspect and the majority of voice parameters had improved, in particular the Voice Handicap Index decreasing from 75 to 9. The perceptual analysis found the voice to be less hoarse and more stable, without breathiness. The case of this patient highlights the therapeutic potential of ADSVF for such applications (trial registration, ClinicalTrials.gov NCT02622464; registered 4 December 2015).
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spelling pubmed-60629672018-07-31 Autologous adipose-derived stromal vascular fraction and scarred vocal folds: first clinical case report Mattei, Alexia Magalon, Jérémy Bertrand, Baptiste Grimaud, Fanny Revis, Joana Velier, Mélanie Veran, Julie Dessi, Patrick Sabatier, Florence Giovanni, Antoine Stem Cell Res Ther Short Report Patients with scarred vocal folds (congenitally or following phonosurgery) are currently difficult to treat and present a dysphonia, often disabling in daily life. Several therapies are available on the market but the results of these are often disappointing. The autologous adipose-derived stromal vascular fraction (ADSVF) is recognized as an easily accessible source of cells with angiogenic, anti-inflammatory, immunomodulatory, and regenerative properties. We present here the case of a 43-year-old woman who had a severe dysphonia associated with scarred vocal folds after a phonosurgery and was resistant to conventional medical and surgical treatments. She received a local administration of autologous ADSVF. The protocol involved, on the same day, adipose tissue extraction, ADSVF preparation, and then local injection (0.45ml of ADSVF in each vocal fold, for a total of 12.2 million ADSVF viable cells). No serious adverse events have been described. One year following the surgery, the laryngoscopic aspect and the majority of voice parameters had improved, in particular the Voice Handicap Index decreasing from 75 to 9. The perceptual analysis found the voice to be less hoarse and more stable, without breathiness. The case of this patient highlights the therapeutic potential of ADSVF for such applications (trial registration, ClinicalTrials.gov NCT02622464; registered 4 December 2015). BioMed Central 2018-07-27 /pmc/articles/PMC6062967/ /pubmed/30053913 http://dx.doi.org/10.1186/s13287-018-0842-0 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Mattei, Alexia
Magalon, Jérémy
Bertrand, Baptiste
Grimaud, Fanny
Revis, Joana
Velier, Mélanie
Veran, Julie
Dessi, Patrick
Sabatier, Florence
Giovanni, Antoine
Autologous adipose-derived stromal vascular fraction and scarred vocal folds: first clinical case report
title Autologous adipose-derived stromal vascular fraction and scarred vocal folds: first clinical case report
title_full Autologous adipose-derived stromal vascular fraction and scarred vocal folds: first clinical case report
title_fullStr Autologous adipose-derived stromal vascular fraction and scarred vocal folds: first clinical case report
title_full_unstemmed Autologous adipose-derived stromal vascular fraction and scarred vocal folds: first clinical case report
title_short Autologous adipose-derived stromal vascular fraction and scarred vocal folds: first clinical case report
title_sort autologous adipose-derived stromal vascular fraction and scarred vocal folds: first clinical case report
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6062967/
https://www.ncbi.nlm.nih.gov/pubmed/30053913
http://dx.doi.org/10.1186/s13287-018-0842-0
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