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Severe Pulmonary Hypertension as Initial Presentation of SLE: A Case Report and Literature Review

Severe pulmonary artery hypertension (PAH) is a rare initial presentation of systemic lupus erythematosus (SLE). SLE associated with PAH carries worse prognosis that isolated SLE. However, there has been improvement in mortality of the patients in the recent years owing to newer treatment options av...

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Autores principales: Kiani, Rabia, Siddiqui, Muhammad Danial, Tantoush, Hamza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7245690/
https://www.ncbi.nlm.nih.gov/pubmed/32509370
http://dx.doi.org/10.1155/2020/6014572
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author Kiani, Rabia
Siddiqui, Muhammad Danial
Tantoush, Hamza
author_facet Kiani, Rabia
Siddiqui, Muhammad Danial
Tantoush, Hamza
author_sort Kiani, Rabia
collection PubMed
description Severe pulmonary artery hypertension (PAH) is a rare initial presentation of systemic lupus erythematosus (SLE). SLE associated with PAH carries worse prognosis that isolated SLE. However, there has been improvement in mortality of the patients in the recent years owing to newer treatment options available. Early recognition remains of prime importance. We present here a case of young female who presented with severe pulmonary hypertension with right heart failure leading to cardiogenic shock and was found to have SLE. She was started on appropriate treatment; however, given the severity of her illness, the patient did not survive. This case highlights the importance of early recognition and prompt treatment of SLE-associated PAH, which might improve the survival rate in the patients.
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spelling pubmed-72456902020-06-05 Severe Pulmonary Hypertension as Initial Presentation of SLE: A Case Report and Literature Review Kiani, Rabia Siddiqui, Muhammad Danial Tantoush, Hamza Case Rep Rheumatol Case Report Severe pulmonary artery hypertension (PAH) is a rare initial presentation of systemic lupus erythematosus (SLE). SLE associated with PAH carries worse prognosis that isolated SLE. However, there has been improvement in mortality of the patients in the recent years owing to newer treatment options available. Early recognition remains of prime importance. We present here a case of young female who presented with severe pulmonary hypertension with right heart failure leading to cardiogenic shock and was found to have SLE. She was started on appropriate treatment; however, given the severity of her illness, the patient did not survive. This case highlights the importance of early recognition and prompt treatment of SLE-associated PAH, which might improve the survival rate in the patients. Hindawi 2020-05-15 /pmc/articles/PMC7245690/ /pubmed/32509370 http://dx.doi.org/10.1155/2020/6014572 Text en Copyright © 2020 Rabia Kiani et al. http://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
Kiani, Rabia
Siddiqui, Muhammad Danial
Tantoush, Hamza
Severe Pulmonary Hypertension as Initial Presentation of SLE: A Case Report and Literature Review
title Severe Pulmonary Hypertension as Initial Presentation of SLE: A Case Report and Literature Review
title_full Severe Pulmonary Hypertension as Initial Presentation of SLE: A Case Report and Literature Review
title_fullStr Severe Pulmonary Hypertension as Initial Presentation of SLE: A Case Report and Literature Review
title_full_unstemmed Severe Pulmonary Hypertension as Initial Presentation of SLE: A Case Report and Literature Review
title_short Severe Pulmonary Hypertension as Initial Presentation of SLE: A Case Report and Literature Review
title_sort severe pulmonary hypertension as initial presentation of sle: a case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7245690/
https://www.ncbi.nlm.nih.gov/pubmed/32509370
http://dx.doi.org/10.1155/2020/6014572
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