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Rapid aneurysm growth and rupture in systemic lupus erythematosus

BACKGROUND: Subarachnoid hemorrhage (SAH) due to intracranial aneurysm rupture is a major neurosurgical emergency associated with significant morbidity and mortality. Rapid aneurysm growth is associated with rupture. Systemic lupus erythematosus (SLE) is a multi-system autoimmune disorder whose comp...

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Autores principales: Graffeo, Christopher S., Tanweer, Omar, Nieves, Cesar Fors, Belmont, H. Michael, Izmirly, Peter M., Becske, Tibor, Huang, Paul P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310132/
https://www.ncbi.nlm.nih.gov/pubmed/25657862
http://dx.doi.org/10.4103/2152-7806.149617
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author Graffeo, Christopher S.
Tanweer, Omar
Nieves, Cesar Fors
Belmont, H. Michael
Izmirly, Peter M.
Becske, Tibor
Huang, Paul P.
author_facet Graffeo, Christopher S.
Tanweer, Omar
Nieves, Cesar Fors
Belmont, H. Michael
Izmirly, Peter M.
Becske, Tibor
Huang, Paul P.
author_sort Graffeo, Christopher S.
collection PubMed
description BACKGROUND: Subarachnoid hemorrhage (SAH) due to intracranial aneurysm rupture is a major neurosurgical emergency associated with significant morbidity and mortality. Rapid aneurysm growth is associated with rupture. Systemic lupus erythematosus (SLE) is a multi-system autoimmune disorder whose complications can include cerebral vasculitis and vasculopathy. Intracranial aneurysms are not known to occur more frequently in SLE patients than the general population; however, aneurysm growth rates have not been studied in SLE. CASE DESCRIPTION: We present a 43-year-old female with SLE on prednisone, hydroxychloroquine, and azathioprine with moderate disease activity who presented with severe, acute-onset headache and was found to have Hunt and Hess grade II SAH due to rupture of an 8 mm saccular anterior communicating artery (ACoA) aneurysm. The patient developed severe vasospasm, re-ruptured, and was taken for angiography and embolization, which was challenging due to a high degree of vasospasm and arterial stenosis. Review of imaging from less than 2 years prior demonstrated a normal ACoA complex without evidence of an aneurysm. CONCLUSION: We review the literature and discuss the risk factors and pathophysiology of rapid aneurysm growth and rupture, as well as the pathologic vascular changes associated with SLE. Although SLE patients do not develop intracranial aneurysm at an increased rate, these changes may predispose them to higher incidence of growth and rupture. This possibility-coupled with increased morbidity and mortality of SAH in SLE-suggests that SAH should be considered in SLE patients presenting with headache, and advocates for more aggressive treatment of SLE patients with unruptured aneurysms.
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spelling pubmed-43101322015-02-05 Rapid aneurysm growth and rupture in systemic lupus erythematosus Graffeo, Christopher S. Tanweer, Omar Nieves, Cesar Fors Belmont, H. Michael Izmirly, Peter M. Becske, Tibor Huang, Paul P. Surg Neurol Int Case Report BACKGROUND: Subarachnoid hemorrhage (SAH) due to intracranial aneurysm rupture is a major neurosurgical emergency associated with significant morbidity and mortality. Rapid aneurysm growth is associated with rupture. Systemic lupus erythematosus (SLE) is a multi-system autoimmune disorder whose complications can include cerebral vasculitis and vasculopathy. Intracranial aneurysms are not known to occur more frequently in SLE patients than the general population; however, aneurysm growth rates have not been studied in SLE. CASE DESCRIPTION: We present a 43-year-old female with SLE on prednisone, hydroxychloroquine, and azathioprine with moderate disease activity who presented with severe, acute-onset headache and was found to have Hunt and Hess grade II SAH due to rupture of an 8 mm saccular anterior communicating artery (ACoA) aneurysm. The patient developed severe vasospasm, re-ruptured, and was taken for angiography and embolization, which was challenging due to a high degree of vasospasm and arterial stenosis. Review of imaging from less than 2 years prior demonstrated a normal ACoA complex without evidence of an aneurysm. CONCLUSION: We review the literature and discuss the risk factors and pathophysiology of rapid aneurysm growth and rupture, as well as the pathologic vascular changes associated with SLE. Although SLE patients do not develop intracranial aneurysm at an increased rate, these changes may predispose them to higher incidence of growth and rupture. This possibility-coupled with increased morbidity and mortality of SAH in SLE-suggests that SAH should be considered in SLE patients presenting with headache, and advocates for more aggressive treatment of SLE patients with unruptured aneurysms. Medknow Publications & Media Pvt Ltd 2015-01-20 /pmc/articles/PMC4310132/ /pubmed/25657862 http://dx.doi.org/10.4103/2152-7806.149617 Text en Copyright: © 2015 Graffeo CS. http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Case Report
Graffeo, Christopher S.
Tanweer, Omar
Nieves, Cesar Fors
Belmont, H. Michael
Izmirly, Peter M.
Becske, Tibor
Huang, Paul P.
Rapid aneurysm growth and rupture in systemic lupus erythematosus
title Rapid aneurysm growth and rupture in systemic lupus erythematosus
title_full Rapid aneurysm growth and rupture in systemic lupus erythematosus
title_fullStr Rapid aneurysm growth and rupture in systemic lupus erythematosus
title_full_unstemmed Rapid aneurysm growth and rupture in systemic lupus erythematosus
title_short Rapid aneurysm growth and rupture in systemic lupus erythematosus
title_sort rapid aneurysm growth and rupture in systemic lupus erythematosus
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4310132/
https://www.ncbi.nlm.nih.gov/pubmed/25657862
http://dx.doi.org/10.4103/2152-7806.149617
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