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Ischemic stroke in a young patient with Fahr’s disease: a case report
BACKGROUND: Fahr’s disease is a rare neurodegenerative disorder characterized by diffuse intracranial calcium deposition and associated cell loss mainly in bilateral basal ganglia and dentate nuclei of the cerebellum. Subarachnoid hemorrhage and epileptic syncope had been reported as acute presentat...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782297/ https://www.ncbi.nlm.nih.gov/pubmed/26951767 http://dx.doi.org/10.1186/s12883-016-0557-8 |
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author | Yang, Chih-Sheng Lo, Chung-Ping Wu, Man-Chun |
author_facet | Yang, Chih-Sheng Lo, Chung-Ping Wu, Man-Chun |
author_sort | Yang, Chih-Sheng |
collection | PubMed |
description | BACKGROUND: Fahr’s disease is a rare neurodegenerative disorder characterized by diffuse intracranial calcium deposition and associated cell loss mainly in bilateral basal ganglia and dentate nuclei of the cerebellum. Subarachnoid hemorrhage and epileptic syncope had been reported as acute presentation of Fahr’s disease. We here report a 36-year-old male Indonesian diagnosed as Fahr’s disease presenting with young-onset ischemic stroke. CASE PRESENTATION: A 36-year-old male Indonesian without prior systemic disease or neurologic disorder presented with young-onset ischemic stroke involving the right posterior limb of internal capsule. Brain computed tomography and magnetic resonance imaging demonstrated symmetric calcifications in bilateral basal ganglia, internal capsules, cerebellar dentate nuclei, thalami, cerebral white matter, which were all consistent with Fahr’s disease. The laboratory studies excluded the presence of other pathologic processes leading to secondary intracranial calcification. Other young stroke surveys were unremarkable. After medical treatment and sustained physical rehabilitation for 3 months, he recovered to carry out daily activities independently. CONCLUSION: We present ischemic stroke in a young patient with sporadic Fahr’s disease. The differentiation between Fahr’s disease and Fahr’s syndrome is specially highlighted when brain CT exhibits diffuse, symmetric calcifications in bilateral basal ganglia, thalami, cerebellar dentate nuclei and cerebral white matter. The association between nonarteriosclerotic vascular calcification and cerebrovascular disease is worth special attention and further investigation. |
format | Online Article Text |
id | pubmed-4782297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47822972016-03-09 Ischemic stroke in a young patient with Fahr’s disease: a case report Yang, Chih-Sheng Lo, Chung-Ping Wu, Man-Chun BMC Neurol Case Report BACKGROUND: Fahr’s disease is a rare neurodegenerative disorder characterized by diffuse intracranial calcium deposition and associated cell loss mainly in bilateral basal ganglia and dentate nuclei of the cerebellum. Subarachnoid hemorrhage and epileptic syncope had been reported as acute presentation of Fahr’s disease. We here report a 36-year-old male Indonesian diagnosed as Fahr’s disease presenting with young-onset ischemic stroke. CASE PRESENTATION: A 36-year-old male Indonesian without prior systemic disease or neurologic disorder presented with young-onset ischemic stroke involving the right posterior limb of internal capsule. Brain computed tomography and magnetic resonance imaging demonstrated symmetric calcifications in bilateral basal ganglia, internal capsules, cerebellar dentate nuclei, thalami, cerebral white matter, which were all consistent with Fahr’s disease. The laboratory studies excluded the presence of other pathologic processes leading to secondary intracranial calcification. Other young stroke surveys were unremarkable. After medical treatment and sustained physical rehabilitation for 3 months, he recovered to carry out daily activities independently. CONCLUSION: We present ischemic stroke in a young patient with sporadic Fahr’s disease. The differentiation between Fahr’s disease and Fahr’s syndrome is specially highlighted when brain CT exhibits diffuse, symmetric calcifications in bilateral basal ganglia, thalami, cerebellar dentate nuclei and cerebral white matter. The association between nonarteriosclerotic vascular calcification and cerebrovascular disease is worth special attention and further investigation. BioMed Central 2016-03-08 /pmc/articles/PMC4782297/ /pubmed/26951767 http://dx.doi.org/10.1186/s12883-016-0557-8 Text en © Yang et al. 2016 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 Yang, Chih-Sheng Lo, Chung-Ping Wu, Man-Chun Ischemic stroke in a young patient with Fahr’s disease: a case report |
title | Ischemic stroke in a young patient with Fahr’s disease: a case report |
title_full | Ischemic stroke in a young patient with Fahr’s disease: a case report |
title_fullStr | Ischemic stroke in a young patient with Fahr’s disease: a case report |
title_full_unstemmed | Ischemic stroke in a young patient with Fahr’s disease: a case report |
title_short | Ischemic stroke in a young patient with Fahr’s disease: a case report |
title_sort | ischemic stroke in a young patient with fahr’s disease: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782297/ https://www.ncbi.nlm.nih.gov/pubmed/26951767 http://dx.doi.org/10.1186/s12883-016-0557-8 |
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