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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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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. |
format | Online Article Text |
id | pubmed-4123257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
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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