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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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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. |
format | Online Article Text |
id | pubmed-5102707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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