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An Interesting Case of Moyamoya Disease, a Rare Cause of Transient Ischemic Attacks
Moyamoya disease is a rare, chronic, idiopathic progressive disease characterized by irreversible vascular occlusion of the vessels of the Circle of Willis. The disease was initially considered to be limited to the East Asian population, but now the disease is being reported all over the globe in pe...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7489789/ https://www.ncbi.nlm.nih.gov/pubmed/32944454 http://dx.doi.org/10.7759/cureus.9736 |
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author | Sapra, Amit Bhandari, Priyanka Dix, Rebecca Sharma, Shivani Ranjit, Eukesh |
author_facet | Sapra, Amit Bhandari, Priyanka Dix, Rebecca Sharma, Shivani Ranjit, Eukesh |
author_sort | Sapra, Amit |
collection | PubMed |
description | Moyamoya disease is a rare, chronic, idiopathic progressive disease characterized by irreversible vascular occlusion of the vessels of the Circle of Willis. The disease was initially considered to be limited to the East Asian population, but now the disease is being reported all over the globe in people of multiple ethnicities. It is crucial that clinicians are aware of the disease and its presentation to prevent under-recognition of the condition. We describe the case of a 44-year-old Caucasian female with a history of hypertension, depression, gastroesophageal reflux disease (GERD), and morbid obesity diagnosed with Moyamoya disease after she presented to the emergency department with recurrent stroke-like symptoms. |
format | Online Article Text |
id | pubmed-7489789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-74897892020-09-16 An Interesting Case of Moyamoya Disease, a Rare Cause of Transient Ischemic Attacks Sapra, Amit Bhandari, Priyanka Dix, Rebecca Sharma, Shivani Ranjit, Eukesh Cureus Family/General Practice Moyamoya disease is a rare, chronic, idiopathic progressive disease characterized by irreversible vascular occlusion of the vessels of the Circle of Willis. The disease was initially considered to be limited to the East Asian population, but now the disease is being reported all over the globe in people of multiple ethnicities. It is crucial that clinicians are aware of the disease and its presentation to prevent under-recognition of the condition. We describe the case of a 44-year-old Caucasian female with a history of hypertension, depression, gastroesophageal reflux disease (GERD), and morbid obesity diagnosed with Moyamoya disease after she presented to the emergency department with recurrent stroke-like symptoms. Cureus 2020-08-14 /pmc/articles/PMC7489789/ /pubmed/32944454 http://dx.doi.org/10.7759/cureus.9736 Text en Copyright © 2020, Sapra et al. http://creativecommons.org/licenses/by/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 | Family/General Practice Sapra, Amit Bhandari, Priyanka Dix, Rebecca Sharma, Shivani Ranjit, Eukesh An Interesting Case of Moyamoya Disease, a Rare Cause of Transient Ischemic Attacks |
title | An Interesting Case of Moyamoya Disease, a Rare Cause of Transient Ischemic Attacks |
title_full | An Interesting Case of Moyamoya Disease, a Rare Cause of Transient Ischemic Attacks |
title_fullStr | An Interesting Case of Moyamoya Disease, a Rare Cause of Transient Ischemic Attacks |
title_full_unstemmed | An Interesting Case of Moyamoya Disease, a Rare Cause of Transient Ischemic Attacks |
title_short | An Interesting Case of Moyamoya Disease, a Rare Cause of Transient Ischemic Attacks |
title_sort | interesting case of moyamoya disease, a rare cause of transient ischemic attacks |
topic | Family/General Practice |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7489789/ https://www.ncbi.nlm.nih.gov/pubmed/32944454 http://dx.doi.org/10.7759/cureus.9736 |
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