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Diffuse idiopathic intracranial fusiform aneurysm development. Case report and literature review

BACKGROUND: Fusiform intracranial aneurysms (FIAs) are uncommon lesions representing less than 15% of all intracranial aneurysms in most large series. Their etiology has been linked to a variety of causes including atherosclerosis, fibromuscular dysplasia, cystic medial necrosis, connective tissue d...

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Autores principales: Nussbaum, Eric S., Defillo, Archie, Mcdonald, William, Hanson, Sandra, Zelensky, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4123257/
https://www.ncbi.nlm.nih.gov/pubmed/25101202
http://dx.doi.org/10.4103/2152-7806.136702
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author Nussbaum, Eric S.
Defillo, Archie
Mcdonald, William
Hanson, Sandra
Zelensky, Andrea
author_facet Nussbaum, Eric S.
Defillo, Archie
Mcdonald, William
Hanson, Sandra
Zelensky, Andrea
author_sort Nussbaum, Eric S.
collection PubMed
description BACKGROUND: Fusiform intracranial aneurysms (FIAs) are uncommon lesions representing less than 15% of all intracranial aneurysms in most large series. Their etiology has been linked to a variety of causes including atherosclerosis, fibromuscular dysplasia, cystic medial necrosis, connective tissue disease, hypertension, diabetes, hyperlipidemia, infection, cardiac myxoma, oral contraceptive use, vasculitis, and lymphoproliferative disorders. The finding of numerous lesions in a single patient is distinctly uncommon. CASE DESCRIPTION: We describe the unique case of a 47-year-old female who developed multiple FIAs over a 6-year period without an obvious underlying pathology. The patient's medical history was significant for obesity, migraine headaches, insomnia, breast cancer, and chronic skin rash. Various diagnoses were explored including infectious etiologies, autoimmune vasculopathies, malignancy-related causes, connective tissue disorders, and underlying genetic conditions. However, all investigations, including aneurysm wall and skin biopsies were negative or deemed noncontributory toward making a definitive diagnosis. CONCLUSION: We report an unusual case of a patient with a normal cerebral angiogram developing numerous, FIAs without obvious underlying etiology over a 6-year period. Close clinical and radiological follow-up is recommended in this case because the natural history of the disease is unclear at this point. The literature regarding potential causes of multiple fusiform intracranial aneuryms is reviewed.
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spelling pubmed-41232572014-08-06 Diffuse idiopathic intracranial fusiform aneurysm development. Case report and literature review Nussbaum, Eric S. Defillo, Archie Mcdonald, William Hanson, Sandra Zelensky, Andrea Surg Neurol Int Case Report BACKGROUND: Fusiform intracranial aneurysms (FIAs) are uncommon lesions representing less than 15% of all intracranial aneurysms in most large series. Their etiology has been linked to a variety of causes including atherosclerosis, fibromuscular dysplasia, cystic medial necrosis, connective tissue disease, hypertension, diabetes, hyperlipidemia, infection, cardiac myxoma, oral contraceptive use, vasculitis, and lymphoproliferative disorders. The finding of numerous lesions in a single patient is distinctly uncommon. CASE DESCRIPTION: We describe the unique case of a 47-year-old female who developed multiple FIAs over a 6-year period without an obvious underlying pathology. The patient's medical history was significant for obesity, migraine headaches, insomnia, breast cancer, and chronic skin rash. Various diagnoses were explored including infectious etiologies, autoimmune vasculopathies, malignancy-related causes, connective tissue disorders, and underlying genetic conditions. However, all investigations, including aneurysm wall and skin biopsies were negative or deemed noncontributory toward making a definitive diagnosis. CONCLUSION: We report an unusual case of a patient with a normal cerebral angiogram developing numerous, FIAs without obvious underlying etiology over a 6-year period. Close clinical and radiological follow-up is recommended in this case because the natural history of the disease is unclear at this point. The literature regarding potential causes of multiple fusiform intracranial aneuryms is reviewed. Medknow Publications & Media Pvt Ltd 2014-07-11 /pmc/articles/PMC4123257/ /pubmed/25101202 http://dx.doi.org/10.4103/2152-7806.136702 Text en Copyright: © 2014 Nussbaum ES 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
Nussbaum, Eric S.
Defillo, Archie
Mcdonald, William
Hanson, Sandra
Zelensky, Andrea
Diffuse idiopathic intracranial fusiform aneurysm development. Case report and literature review
title Diffuse idiopathic intracranial fusiform aneurysm development. Case report and literature review
title_full Diffuse idiopathic intracranial fusiform aneurysm development. Case report and literature review
title_fullStr Diffuse idiopathic intracranial fusiform aneurysm development. Case report and literature review
title_full_unstemmed Diffuse idiopathic intracranial fusiform aneurysm development. Case report and literature review
title_short Diffuse idiopathic intracranial fusiform aneurysm development. Case report and literature review
title_sort diffuse idiopathic intracranial fusiform aneurysm development. case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4123257/
https://www.ncbi.nlm.nih.gov/pubmed/25101202
http://dx.doi.org/10.4103/2152-7806.136702
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