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Kidney transplantation in infantile myofibromatosis and fibromuscular dysplasia: a case report

INTRODUCTION: We report what we believe to be the first case of a child affected by two rare vascular diseases complicated by kidney failure and successfully treated by kidney transplantation. CASE PRESENTATION: A 3-year-old Caucasian girl with fibromuscular dysplasia and infantile myofibromatosis p...

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Autores principales: Frezin, Julie, Fusaro, Fabio, Reding, Raymond, Godefroid, Nathalie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4658745/
https://www.ncbi.nlm.nih.gov/pubmed/26603035
http://dx.doi.org/10.1186/s13256-015-0756-8
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author Frezin, Julie
Fusaro, Fabio
Reding, Raymond
Godefroid, Nathalie
author_facet Frezin, Julie
Fusaro, Fabio
Reding, Raymond
Godefroid, Nathalie
author_sort Frezin, Julie
collection PubMed
description INTRODUCTION: We report what we believe to be the first case of a child affected by two rare vascular diseases complicated by kidney failure and successfully treated by kidney transplantation. CASE PRESENTATION: A 3-year-old Caucasian girl with fibromuscular dysplasia and infantile myofibromatosis presented with arterial hypertension and renal failure. She received a deceased donor kidney transplantation distal to an iliac graft. The technical peculiarities of this transplantation are described, as well as her favorable long-term outcome. CONCLUSION: Kidney transplantation may be considered in a patient with vascular diseases and a history of iliac surgery.
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spelling pubmed-46587452015-11-26 Kidney transplantation in infantile myofibromatosis and fibromuscular dysplasia: a case report Frezin, Julie Fusaro, Fabio Reding, Raymond Godefroid, Nathalie J Med Case Rep Case Report INTRODUCTION: We report what we believe to be the first case of a child affected by two rare vascular diseases complicated by kidney failure and successfully treated by kidney transplantation. CASE PRESENTATION: A 3-year-old Caucasian girl with fibromuscular dysplasia and infantile myofibromatosis presented with arterial hypertension and renal failure. She received a deceased donor kidney transplantation distal to an iliac graft. The technical peculiarities of this transplantation are described, as well as her favorable long-term outcome. CONCLUSION: Kidney transplantation may be considered in a patient with vascular diseases and a history of iliac surgery. BioMed Central 2015-11-25 /pmc/articles/PMC4658745/ /pubmed/26603035 http://dx.doi.org/10.1186/s13256-015-0756-8 Text en © Frezin et al. 2015 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
Frezin, Julie
Fusaro, Fabio
Reding, Raymond
Godefroid, Nathalie
Kidney transplantation in infantile myofibromatosis and fibromuscular dysplasia: a case report
title Kidney transplantation in infantile myofibromatosis and fibromuscular dysplasia: a case report
title_full Kidney transplantation in infantile myofibromatosis and fibromuscular dysplasia: a case report
title_fullStr Kidney transplantation in infantile myofibromatosis and fibromuscular dysplasia: a case report
title_full_unstemmed Kidney transplantation in infantile myofibromatosis and fibromuscular dysplasia: a case report
title_short Kidney transplantation in infantile myofibromatosis and fibromuscular dysplasia: a case report
title_sort kidney transplantation in infantile myofibromatosis and fibromuscular dysplasia: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4658745/
https://www.ncbi.nlm.nih.gov/pubmed/26603035
http://dx.doi.org/10.1186/s13256-015-0756-8
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