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Challenges in diagnosing and treating a patient with renal artery fibromuscular dysplasia: case report

BACKGROUND: We present a patient with history of sinus venous thrombosis and hypertension during the last year. Her blood pressure was not controlled despite drugs, diet, and exercise. She denied symptoms. She does not smoke nor drink alcohol. Her body mass index was 20 kg/m(2), NYHA Class I/IV. CAS...

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Autores principales: Rodríguez Goyes, Julio César, Jaramillo Gómez, Nicolás Ignacio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439373/
https://www.ncbi.nlm.nih.gov/pubmed/31020224
http://dx.doi.org/10.1093/ehjcr/yty144
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author Rodríguez Goyes, Julio César
Jaramillo Gómez, Nicolás Ignacio
author_facet Rodríguez Goyes, Julio César
Jaramillo Gómez, Nicolás Ignacio
author_sort Rodríguez Goyes, Julio César
collection PubMed
description BACKGROUND: We present a patient with history of sinus venous thrombosis and hypertension during the last year. Her blood pressure was not controlled despite drugs, diet, and exercise. She denied symptoms. She does not smoke nor drink alcohol. Her body mass index was 20 kg/m(2), NYHA Class I/IV. CASE SUMMARY: A 40-year-old Latin-American female patient, concerned because despite taking verapamil 160 mg/day, losartan 100 mg/day, and hydrochlorothiazide 25 mg/day her diastolic blood pressure was over 100 mmHg. Routine serum and urine lab tests and a transthoracic echocardiogram were done and were normal. The treatment was increased over the next consultations but without control of her blood pressure. She developed resistant hypertension, and she was taking four antihypertensive drugs and two diuretics. A first renal artery Doppler was normal. Because of a high clinical suspicion a renal angio-CT was performed showing bilateral fibromuscular dysplasia. The patient underwent a renal artery angioplasty with balloon with excellent results and better control of her blood pressure after the procedure. Over the next month, her doctors were able to decrease her treatment to two drugs at intermediate doses. Currently, she is doing well and asymptomatic. DISCUSSION: Renal artery fibromuscular dysplasia (FMD) could be a challenging disease to be diagnosed. Patients with this condition may suffer from symptomatic and resistant hypertension. Many patients do not have abnormalities on their physical exam or in the routine lab tests. Treatment includes renal artery angioplasty if patient is symptomatic and blood pressure is resistant.
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spelling pubmed-64393732019-04-24 Challenges in diagnosing and treating a patient with renal artery fibromuscular dysplasia: case report Rodríguez Goyes, Julio César Jaramillo Gómez, Nicolás Ignacio Eur Heart J Case Rep Case Reports BACKGROUND: We present a patient with history of sinus venous thrombosis and hypertension during the last year. Her blood pressure was not controlled despite drugs, diet, and exercise. She denied symptoms. She does not smoke nor drink alcohol. Her body mass index was 20 kg/m(2), NYHA Class I/IV. CASE SUMMARY: A 40-year-old Latin-American female patient, concerned because despite taking verapamil 160 mg/day, losartan 100 mg/day, and hydrochlorothiazide 25 mg/day her diastolic blood pressure was over 100 mmHg. Routine serum and urine lab tests and a transthoracic echocardiogram were done and were normal. The treatment was increased over the next consultations but without control of her blood pressure. She developed resistant hypertension, and she was taking four antihypertensive drugs and two diuretics. A first renal artery Doppler was normal. Because of a high clinical suspicion a renal angio-CT was performed showing bilateral fibromuscular dysplasia. The patient underwent a renal artery angioplasty with balloon with excellent results and better control of her blood pressure after the procedure. Over the next month, her doctors were able to decrease her treatment to two drugs at intermediate doses. Currently, she is doing well and asymptomatic. DISCUSSION: Renal artery fibromuscular dysplasia (FMD) could be a challenging disease to be diagnosed. Patients with this condition may suffer from symptomatic and resistant hypertension. Many patients do not have abnormalities on their physical exam or in the routine lab tests. Treatment includes renal artery angioplasty if patient is symptomatic and blood pressure is resistant. Oxford University Press 2019-01-09 /pmc/articles/PMC6439373/ /pubmed/31020224 http://dx.doi.org/10.1093/ehjcr/yty144 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the European Society of Cardiology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Reports
Rodríguez Goyes, Julio César
Jaramillo Gómez, Nicolás Ignacio
Challenges in diagnosing and treating a patient with renal artery fibromuscular dysplasia: case report
title Challenges in diagnosing and treating a patient with renal artery fibromuscular dysplasia: case report
title_full Challenges in diagnosing and treating a patient with renal artery fibromuscular dysplasia: case report
title_fullStr Challenges in diagnosing and treating a patient with renal artery fibromuscular dysplasia: case report
title_full_unstemmed Challenges in diagnosing and treating a patient with renal artery fibromuscular dysplasia: case report
title_short Challenges in diagnosing and treating a patient with renal artery fibromuscular dysplasia: case report
title_sort challenges in diagnosing and treating a patient with renal artery fibromuscular dysplasia: case report
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439373/
https://www.ncbi.nlm.nih.gov/pubmed/31020224
http://dx.doi.org/10.1093/ehjcr/yty144
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