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Central nervous system vasculopathy caused by Fabry disease: a case report
BACKGROUND: Fabry disease is rare, and the diagnosis is often delayed. Here, we describe a case of Fabry disease resulting in vasculopathy of the central nervous system. Magnetic resonance (MR) black-blood sequence (three-dimensional T1 volumetric isotropic turbo spin echo acquisition), with the uni...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551893/ https://www.ncbi.nlm.nih.gov/pubmed/31170963 http://dx.doi.org/10.1186/s12883-019-1348-9 |
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author | Kong, De-Zheng Lian, Ya-Hui Wang, Lin-Jing Wang, Chun-Mei Meng, Yang-Yang Zhou, Hong-Wei |
author_facet | Kong, De-Zheng Lian, Ya-Hui Wang, Lin-Jing Wang, Chun-Mei Meng, Yang-Yang Zhou, Hong-Wei |
author_sort | Kong, De-Zheng |
collection | PubMed |
description | BACKGROUND: Fabry disease is rare, and the diagnosis is often delayed. Here, we describe a case of Fabry disease resulting in vasculopathy of the central nervous system. Magnetic resonance (MR) black-blood sequence (three-dimensional T1 volumetric isotropic turbo spin echo acquisition), with the unique advantage of imaging the vascular wall, facilitated a clear identification of the vasculopathy. CASE PRESENTATION: A 27-year-old man visited our hospital for the treatment of “ double vision 6d.” After a series of examinations, the patient was diagnosed with Fabry disease, which caused vasculopathy of the central nervous system. Subsequently, the patient was treated with corticosteroids and his symptoms were attenuated. Two months after the initial treatment, the initial lesion in the vascular vessel disappeared, however, a new lesion appeared. Similarly, four months after the initial treatment, although the previous lesion disappeared, a new lesion appeared. CONCLUSIONS: This case highlights that clinicians should use MR black-blood sequence scan in a timely manner in case of young patients with migratory lesions of brain. In case of detection of a vascular lesion in combination with other systemic lesions, the possibility of Fabry disease should be considered. |
format | Online Article Text |
id | pubmed-6551893 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65518932019-06-07 Central nervous system vasculopathy caused by Fabry disease: a case report Kong, De-Zheng Lian, Ya-Hui Wang, Lin-Jing Wang, Chun-Mei Meng, Yang-Yang Zhou, Hong-Wei BMC Neurol Case Report BACKGROUND: Fabry disease is rare, and the diagnosis is often delayed. Here, we describe a case of Fabry disease resulting in vasculopathy of the central nervous system. Magnetic resonance (MR) black-blood sequence (three-dimensional T1 volumetric isotropic turbo spin echo acquisition), with the unique advantage of imaging the vascular wall, facilitated a clear identification of the vasculopathy. CASE PRESENTATION: A 27-year-old man visited our hospital for the treatment of “ double vision 6d.” After a series of examinations, the patient was diagnosed with Fabry disease, which caused vasculopathy of the central nervous system. Subsequently, the patient was treated with corticosteroids and his symptoms were attenuated. Two months after the initial treatment, the initial lesion in the vascular vessel disappeared, however, a new lesion appeared. Similarly, four months after the initial treatment, although the previous lesion disappeared, a new lesion appeared. CONCLUSIONS: This case highlights that clinicians should use MR black-blood sequence scan in a timely manner in case of young patients with migratory lesions of brain. In case of detection of a vascular lesion in combination with other systemic lesions, the possibility of Fabry disease should be considered. BioMed Central 2019-06-06 /pmc/articles/PMC6551893/ /pubmed/31170963 http://dx.doi.org/10.1186/s12883-019-1348-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Kong, De-Zheng Lian, Ya-Hui Wang, Lin-Jing Wang, Chun-Mei Meng, Yang-Yang Zhou, Hong-Wei Central nervous system vasculopathy caused by Fabry disease: a case report |
title | Central nervous system vasculopathy caused by Fabry disease: a case report |
title_full | Central nervous system vasculopathy caused by Fabry disease: a case report |
title_fullStr | Central nervous system vasculopathy caused by Fabry disease: a case report |
title_full_unstemmed | Central nervous system vasculopathy caused by Fabry disease: a case report |
title_short | Central nervous system vasculopathy caused by Fabry disease: a case report |
title_sort | central nervous system vasculopathy caused by fabry disease: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551893/ https://www.ncbi.nlm.nih.gov/pubmed/31170963 http://dx.doi.org/10.1186/s12883-019-1348-9 |
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