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De Novo intracerebral aneurysm in a child with acquired immunodeficiency syndrome

Human immunodeficiency virus (HIV) infection associated aneurysmal vasculopathy is a rare complication of HIV infection affecting the pediatric and adult population. We present a case of a 7-year-old male child known to have a congenitally acquired HIV infection presenting with a ruptured left dista...

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Autores principales: Bakhaidar, Mohamad G., Ahamed, Naushad A., Almekhlafi, Mohammed A., Baeesa, Saleh S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Riyadh : Armed Forces Hospital 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4710332/
https://www.ncbi.nlm.nih.gov/pubmed/26166600
http://dx.doi.org/10.17712/nsj.2015.3.20150064
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author Bakhaidar, Mohamad G.
Ahamed, Naushad A.
Almekhlafi, Mohammed A.
Baeesa, Saleh S.
author_facet Bakhaidar, Mohamad G.
Ahamed, Naushad A.
Almekhlafi, Mohammed A.
Baeesa, Saleh S.
author_sort Bakhaidar, Mohamad G.
collection PubMed
description Human immunodeficiency virus (HIV) infection associated aneurysmal vasculopathy is a rare complication of HIV infection affecting the pediatric and adult population. We present a case of a 7-year-old male child known to have a congenitally acquired HIV infection presenting with a ruptured left distal internal carotid artery fusiform aneurysm that was diagnosed on MRI scans 6 months prior to his presentation. He underwent craniotomy and successful aneurysm reconstruction. He had uncomplicated postoperative course and experienced a good recovery. This case is among the few reported pediatric cases of HIV-associated cerebral arteriopathy to undergo surgery. We also reviewed the relevant literature of this rare condition.
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spelling pubmed-47103322016-02-02 De Novo intracerebral aneurysm in a child with acquired immunodeficiency syndrome Bakhaidar, Mohamad G. Ahamed, Naushad A. Almekhlafi, Mohammed A. Baeesa, Saleh S. Neurosciences (Riyadh) Case Report Human immunodeficiency virus (HIV) infection associated aneurysmal vasculopathy is a rare complication of HIV infection affecting the pediatric and adult population. We present a case of a 7-year-old male child known to have a congenitally acquired HIV infection presenting with a ruptured left distal internal carotid artery fusiform aneurysm that was diagnosed on MRI scans 6 months prior to his presentation. He underwent craniotomy and successful aneurysm reconstruction. He had uncomplicated postoperative course and experienced a good recovery. This case is among the few reported pediatric cases of HIV-associated cerebral arteriopathy to undergo surgery. We also reviewed the relevant literature of this rare condition. Riyadh : Armed Forces Hospital 2015-07 /pmc/articles/PMC4710332/ /pubmed/26166600 http://dx.doi.org/10.17712/nsj.2015.3.20150064 Text en Copyright: © Neurosciences Neurosciences is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work.
spellingShingle Case Report
Bakhaidar, Mohamad G.
Ahamed, Naushad A.
Almekhlafi, Mohammed A.
Baeesa, Saleh S.
De Novo intracerebral aneurysm in a child with acquired immunodeficiency syndrome
title De Novo intracerebral aneurysm in a child with acquired immunodeficiency syndrome
title_full De Novo intracerebral aneurysm in a child with acquired immunodeficiency syndrome
title_fullStr De Novo intracerebral aneurysm in a child with acquired immunodeficiency syndrome
title_full_unstemmed De Novo intracerebral aneurysm in a child with acquired immunodeficiency syndrome
title_short De Novo intracerebral aneurysm in a child with acquired immunodeficiency syndrome
title_sort de novo intracerebral aneurysm in a child with acquired immunodeficiency syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4710332/
https://www.ncbi.nlm.nih.gov/pubmed/26166600
http://dx.doi.org/10.17712/nsj.2015.3.20150064
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