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A Challenging Case of Fibromuscular Dysplasia in a Transgender Patient: Is There a Hormonal Link?

INTRODUCTION: Fibromuscular dysplasia (FMD) and superior mesenteric artery (SMA) aneurysms are rare vascular conditions. An unusual combination of both diseases is reported. CASE REPORT: A 54 year old woman presented with symptomatic SMA aneurysm. A diagnosis of FMD was made on the basis of computed...

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Autores principales: Shalan, Ahmed, Hughes, Michael, Nicholls, Marcus, Thompson, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033210/
https://www.ncbi.nlm.nih.gov/pubmed/29988870
http://dx.doi.org/10.1016/j.ejvssr.2018.04.002
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author Shalan, Ahmed
Hughes, Michael
Nicholls, Marcus
Thompson, Andrew
author_facet Shalan, Ahmed
Hughes, Michael
Nicholls, Marcus
Thompson, Andrew
author_sort Shalan, Ahmed
collection PubMed
description INTRODUCTION: Fibromuscular dysplasia (FMD) and superior mesenteric artery (SMA) aneurysms are rare vascular conditions. An unusual combination of both diseases is reported. CASE REPORT: A 54 year old woman presented with symptomatic SMA aneurysm. A diagnosis of FMD was made on the basis of computed tomography angiography (CTA). The patient had undergone gender reassignment surgery 10 years previously and continued to use both topical and oral hormonal therapy. The patient received open anatomical bypass through a retroperitoneal approach using great saphenous vein. CONCLUSION: Superior mesenteric artery aneurysms are rare and a diagnosis of FMD should be considered as part of the diagnosis process. Anatomical bypass should be considered carefully in relation to a patient's fitness as well as anatomical suitability.
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spelling pubmed-60332102018-07-09 A Challenging Case of Fibromuscular Dysplasia in a Transgender Patient: Is There a Hormonal Link? Shalan, Ahmed Hughes, Michael Nicholls, Marcus Thompson, Andrew EJVES Short Rep Case Report INTRODUCTION: Fibromuscular dysplasia (FMD) and superior mesenteric artery (SMA) aneurysms are rare vascular conditions. An unusual combination of both diseases is reported. CASE REPORT: A 54 year old woman presented with symptomatic SMA aneurysm. A diagnosis of FMD was made on the basis of computed tomography angiography (CTA). The patient had undergone gender reassignment surgery 10 years previously and continued to use both topical and oral hormonal therapy. The patient received open anatomical bypass through a retroperitoneal approach using great saphenous vein. CONCLUSION: Superior mesenteric artery aneurysms are rare and a diagnosis of FMD should be considered as part of the diagnosis process. Anatomical bypass should be considered carefully in relation to a patient's fitness as well as anatomical suitability. Elsevier 2018-05-08 /pmc/articles/PMC6033210/ /pubmed/29988870 http://dx.doi.org/10.1016/j.ejvssr.2018.04.002 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Shalan, Ahmed
Hughes, Michael
Nicholls, Marcus
Thompson, Andrew
A Challenging Case of Fibromuscular Dysplasia in a Transgender Patient: Is There a Hormonal Link?
title A Challenging Case of Fibromuscular Dysplasia in a Transgender Patient: Is There a Hormonal Link?
title_full A Challenging Case of Fibromuscular Dysplasia in a Transgender Patient: Is There a Hormonal Link?
title_fullStr A Challenging Case of Fibromuscular Dysplasia in a Transgender Patient: Is There a Hormonal Link?
title_full_unstemmed A Challenging Case of Fibromuscular Dysplasia in a Transgender Patient: Is There a Hormonal Link?
title_short A Challenging Case of Fibromuscular Dysplasia in a Transgender Patient: Is There a Hormonal Link?
title_sort challenging case of fibromuscular dysplasia in a transgender patient: is there a hormonal link?
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6033210/
https://www.ncbi.nlm.nih.gov/pubmed/29988870
http://dx.doi.org/10.1016/j.ejvssr.2018.04.002
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