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Perioperative risk assessment for successful kidney transplant in leigh syndrome: a case report

BACKGROUND: Leigh syndrome (LS) is a rare neurodegenerative mitochondrial disorder which typically presents in childhood but has a varied clinical course. Renal involvement such as proximal tubulopathy in patients with mitochondrial disorders has been described. However, end stage renal disease (ESR...

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Autores principales: Ducharlet, Kathryn, Thyagarajan, Dominic, Ierino, Francesco, McMahon, Lawrence P., Lee, Darren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796450/
https://www.ncbi.nlm.nih.gov/pubmed/29390978
http://dx.doi.org/10.1186/s12882-018-0816-6
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author Ducharlet, Kathryn
Thyagarajan, Dominic
Ierino, Francesco
McMahon, Lawrence P.
Lee, Darren
author_facet Ducharlet, Kathryn
Thyagarajan, Dominic
Ierino, Francesco
McMahon, Lawrence P.
Lee, Darren
author_sort Ducharlet, Kathryn
collection PubMed
description BACKGROUND: Leigh syndrome (LS) is a rare neurodegenerative mitochondrial disorder which typically presents in childhood but has a varied clinical course. Renal involvement such as proximal tubulopathy in patients with mitochondrial disorders has been described. However, end stage renal disease (ESRD) is uncommon and literature regarding patients undergoing kidney transplantation is limited. Successful deceased donor renal transplant has not been previously described in a patient with Leigh Syndrome. CASE PRESENTATION: We report a 21-year-old Han Chinese man who presented with limb weakness and unsteady gait, which progressed rapidly over a period of months until he was wheelchair-bound. He subsequently developed ESRD and was commenced on hemodialysis. Investigations revealed a m.13513G > A mutation with clinical and radiological features consistent with LS. His mitochondrial disease stabilised and he underwent a multidisciplinary assessment for deceased donor kidney transplantation to identify and minimise the LS-associated perioperative risks and potential negative effects of immunosuppressants on his LS. Successful kidney transplantation followed with excellent graft function three and a half years post-transplant and improvement in the patient’s physical function. CONCLUSION: This case highlights the importance of careful pre-transplant perioperative risk assessment and post-transplant care in a rare and heterogeneous neurological disease to achieve an ultimately excellent clinical outcome. To our knowledge, this is the first report of successful deceased donor kidney transplant in a patient with known LS.
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spelling pubmed-57964502018-02-12 Perioperative risk assessment for successful kidney transplant in leigh syndrome: a case report Ducharlet, Kathryn Thyagarajan, Dominic Ierino, Francesco McMahon, Lawrence P. Lee, Darren BMC Nephrol Case Report BACKGROUND: Leigh syndrome (LS) is a rare neurodegenerative mitochondrial disorder which typically presents in childhood but has a varied clinical course. Renal involvement such as proximal tubulopathy in patients with mitochondrial disorders has been described. However, end stage renal disease (ESRD) is uncommon and literature regarding patients undergoing kidney transplantation is limited. Successful deceased donor renal transplant has not been previously described in a patient with Leigh Syndrome. CASE PRESENTATION: We report a 21-year-old Han Chinese man who presented with limb weakness and unsteady gait, which progressed rapidly over a period of months until he was wheelchair-bound. He subsequently developed ESRD and was commenced on hemodialysis. Investigations revealed a m.13513G > A mutation with clinical and radiological features consistent with LS. His mitochondrial disease stabilised and he underwent a multidisciplinary assessment for deceased donor kidney transplantation to identify and minimise the LS-associated perioperative risks and potential negative effects of immunosuppressants on his LS. Successful kidney transplantation followed with excellent graft function three and a half years post-transplant and improvement in the patient’s physical function. CONCLUSION: This case highlights the importance of careful pre-transplant perioperative risk assessment and post-transplant care in a rare and heterogeneous neurological disease to achieve an ultimately excellent clinical outcome. To our knowledge, this is the first report of successful deceased donor kidney transplant in a patient with known LS. BioMed Central 2018-02-01 /pmc/articles/PMC5796450/ /pubmed/29390978 http://dx.doi.org/10.1186/s12882-018-0816-6 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 Case Report
Ducharlet, Kathryn
Thyagarajan, Dominic
Ierino, Francesco
McMahon, Lawrence P.
Lee, Darren
Perioperative risk assessment for successful kidney transplant in leigh syndrome: a case report
title Perioperative risk assessment for successful kidney transplant in leigh syndrome: a case report
title_full Perioperative risk assessment for successful kidney transplant in leigh syndrome: a case report
title_fullStr Perioperative risk assessment for successful kidney transplant in leigh syndrome: a case report
title_full_unstemmed Perioperative risk assessment for successful kidney transplant in leigh syndrome: a case report
title_short Perioperative risk assessment for successful kidney transplant in leigh syndrome: a case report
title_sort perioperative risk assessment for successful kidney transplant in leigh syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796450/
https://www.ncbi.nlm.nih.gov/pubmed/29390978
http://dx.doi.org/10.1186/s12882-018-0816-6
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