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‘Smoke in the air’: a rare cerebrovascular cause of neurological signs and symptoms in a young adult
Moyamoya disease is a rare neurological condition that affects children and adults of all ages. It is characterized by chronic, progressive stenosis of the circle of Willis that ultimately leads to the development of extensive collateral vessels. Presenting symptoms are usually due to cerebral ische...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Co-Action Publishing
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4475270/ https://www.ncbi.nlm.nih.gov/pubmed/26091661 http://dx.doi.org/10.3402/jchimp.v5.27664 |
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author | Ismail, Imtiaz Al-Khafaji, Khalid Mutyala, Monica Aggarwal, Saurabh Al-Khafaji, Nawfal Kovacs, Daniela Khosla, Sandeep Arora, Rohit |
author_facet | Ismail, Imtiaz Al-Khafaji, Khalid Mutyala, Monica Aggarwal, Saurabh Al-Khafaji, Nawfal Kovacs, Daniela Khosla, Sandeep Arora, Rohit |
author_sort | Ismail, Imtiaz |
collection | PubMed |
description | Moyamoya disease is a rare neurological condition that affects children and adults of all ages. It is characterized by chronic, progressive stenosis of the circle of Willis that ultimately leads to the development of extensive collateral vessels. Presenting symptoms are usually due to cerebral ischemia or hemorrhage. The Japanese term moyamoya (meaning puffy or obscure) was coined to describe the characteristic ‘smoke in the air’ appearance of these vessels on cerebral angiography. Moyamoya has the highest recorded incidence in Japan (0.28 per 100,000). In the west it is an extremely rare condition with an overall incidence of (0.086 per 100,000) in the Western United States. Etiology for the most part is unknown; however, genetic susceptibility related to RNF213 gene on chromosome 17q25.3 has been suggested. Moyamoya is being diagnosed more frequently in all races with varying clinical manifestations. Moyamoya disease is a rare progressive neurologic condition characterized by occlusion of the cerebral circulation with extensive collaterals recruitment in children and adults. Distinguished radiological findings confirm the diagnosis. Early recognition and swift institution of therapy is vital in order to minimize neurological deficits. We present the case of a 19-year-old African American female who presented with left-sided parastheia, weakness, and headache for 2 days duration. |
format | Online Article Text |
id | pubmed-4475270 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Co-Action Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-44752702015-07-15 ‘Smoke in the air’: a rare cerebrovascular cause of neurological signs and symptoms in a young adult Ismail, Imtiaz Al-Khafaji, Khalid Mutyala, Monica Aggarwal, Saurabh Al-Khafaji, Nawfal Kovacs, Daniela Khosla, Sandeep Arora, Rohit J Community Hosp Intern Med Perspect Case Report Moyamoya disease is a rare neurological condition that affects children and adults of all ages. It is characterized by chronic, progressive stenosis of the circle of Willis that ultimately leads to the development of extensive collateral vessels. Presenting symptoms are usually due to cerebral ischemia or hemorrhage. The Japanese term moyamoya (meaning puffy or obscure) was coined to describe the characteristic ‘smoke in the air’ appearance of these vessels on cerebral angiography. Moyamoya has the highest recorded incidence in Japan (0.28 per 100,000). In the west it is an extremely rare condition with an overall incidence of (0.086 per 100,000) in the Western United States. Etiology for the most part is unknown; however, genetic susceptibility related to RNF213 gene on chromosome 17q25.3 has been suggested. Moyamoya is being diagnosed more frequently in all races with varying clinical manifestations. Moyamoya disease is a rare progressive neurologic condition characterized by occlusion of the cerebral circulation with extensive collaterals recruitment in children and adults. Distinguished radiological findings confirm the diagnosis. Early recognition and swift institution of therapy is vital in order to minimize neurological deficits. We present the case of a 19-year-old African American female who presented with left-sided parastheia, weakness, and headache for 2 days duration. Co-Action Publishing 2015-06-15 /pmc/articles/PMC4475270/ /pubmed/26091661 http://dx.doi.org/10.3402/jchimp.v5.27664 Text en © 2015 Imtiaz Ismail et al. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Ismail, Imtiaz Al-Khafaji, Khalid Mutyala, Monica Aggarwal, Saurabh Al-Khafaji, Nawfal Kovacs, Daniela Khosla, Sandeep Arora, Rohit ‘Smoke in the air’: a rare cerebrovascular cause of neurological signs and symptoms in a young adult |
title | ‘Smoke in the air’: a rare cerebrovascular cause of neurological signs and symptoms in a young adult |
title_full | ‘Smoke in the air’: a rare cerebrovascular cause of neurological signs and symptoms in a young adult |
title_fullStr | ‘Smoke in the air’: a rare cerebrovascular cause of neurological signs and symptoms in a young adult |
title_full_unstemmed | ‘Smoke in the air’: a rare cerebrovascular cause of neurological signs and symptoms in a young adult |
title_short | ‘Smoke in the air’: a rare cerebrovascular cause of neurological signs and symptoms in a young adult |
title_sort | ‘smoke in the air’: a rare cerebrovascular cause of neurological signs and symptoms in a young adult |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4475270/ https://www.ncbi.nlm.nih.gov/pubmed/26091661 http://dx.doi.org/10.3402/jchimp.v5.27664 |
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