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Spontaneous Renal Artery Dissection in a Patient with Neurofibromatosis Type I

We present a case of spontaneous renal artery dissection (SRAD) in a 28-year-old female with history of neurofibromatosis type I (NF-1) treated successfully with endovascular stenting. The clinical presentation, diagnostic testing, and treatment options are discussed. An endovascular approach with s...

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Detalles Bibliográficos
Autores principales: Shammas, Nicolas W., Chammas, Majid Z., Robken, Jon, Coyne, Edmund
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5102707/
https://www.ncbi.nlm.nih.gov/pubmed/27867667
http://dx.doi.org/10.1155/2016/4593932
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author Shammas, Nicolas W.
Chammas, Majid Z.
Robken, Jon
Coyne, Edmund
author_facet Shammas, Nicolas W.
Chammas, Majid Z.
Robken, Jon
Coyne, Edmund
author_sort Shammas, Nicolas W.
collection PubMed
description We present a case of spontaneous renal artery dissection (SRAD) in a 28-year-old female with history of neurofibromatosis type I (NF-1) treated successfully with endovascular stenting. The clinical presentation, diagnostic testing, and treatment options are discussed. An endovascular approach with stenting was successfully performed after failure of medical treatment with subcutaneous low molecular weight heparin. Patient's blood pressure and symptoms improved significantly. This may be the first reported case of SRAD in a patient with NF-1 successfully treated with endovascular stenting.
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spelling pubmed-51027072016-11-20 Spontaneous Renal Artery Dissection in a Patient with Neurofibromatosis Type I Shammas, Nicolas W. Chammas, Majid Z. Robken, Jon Coyne, Edmund Case Rep Cardiol Case Report We present a case of spontaneous renal artery dissection (SRAD) in a 28-year-old female with history of neurofibromatosis type I (NF-1) treated successfully with endovascular stenting. The clinical presentation, diagnostic testing, and treatment options are discussed. An endovascular approach with stenting was successfully performed after failure of medical treatment with subcutaneous low molecular weight heparin. Patient's blood pressure and symptoms improved significantly. This may be the first reported case of SRAD in a patient with NF-1 successfully treated with endovascular stenting. Hindawi Publishing Corporation 2016 2016-10-27 /pmc/articles/PMC5102707/ /pubmed/27867667 http://dx.doi.org/10.1155/2016/4593932 Text en Copyright © 2016 Nicolas W. Shammas et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Shammas, Nicolas W.
Chammas, Majid Z.
Robken, Jon
Coyne, Edmund
Spontaneous Renal Artery Dissection in a Patient with Neurofibromatosis Type I
title Spontaneous Renal Artery Dissection in a Patient with Neurofibromatosis Type I
title_full Spontaneous Renal Artery Dissection in a Patient with Neurofibromatosis Type I
title_fullStr Spontaneous Renal Artery Dissection in a Patient with Neurofibromatosis Type I
title_full_unstemmed Spontaneous Renal Artery Dissection in a Patient with Neurofibromatosis Type I
title_short Spontaneous Renal Artery Dissection in a Patient with Neurofibromatosis Type I
title_sort spontaneous renal artery dissection in a patient with neurofibromatosis type i
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5102707/
https://www.ncbi.nlm.nih.gov/pubmed/27867667
http://dx.doi.org/10.1155/2016/4593932
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