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Magnetic resonance imaging pontine signal abnormality in neurological Wilson disease: A case report
KEY CLINICAL MESSAGE: WD is diagnosed with the help of a brain MRI, which frequently reveals hyperintensities in the lentiform nucleus. But occasionally, high signals can be seen in the pons, thalamus, and midbrain. ABSTRACT: Wilson disease is a rare inherited disorder due to impaired copper excreti...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10457478/ https://www.ncbi.nlm.nih.gov/pubmed/37636888 http://dx.doi.org/10.1002/ccr3.7851 |
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author | Gajurel, Bikram Prasad Karki, Susmin Parajuli, Asmita Khanal, Sunil Babu |
author_facet | Gajurel, Bikram Prasad Karki, Susmin Parajuli, Asmita Khanal, Sunil Babu |
author_sort | Gajurel, Bikram Prasad |
collection | PubMed |
description | KEY CLINICAL MESSAGE: WD is diagnosed with the help of a brain MRI, which frequently reveals hyperintensities in the lentiform nucleus. But occasionally, high signals can be seen in the pons, thalamus, and midbrain. ABSTRACT: Wilson disease is a rare inherited disorder due to impaired copper excretion. The brain MRI mainly shows hyperintensities in the lentiform nucleus. We report the case of an 18 years old female diagnosed with neurological Wilson disease, presenting with uncommon brain MRI hyperintensities, predominantly in the pons, thalamus, and midbrain. |
format | Online Article Text |
id | pubmed-10457478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104574782023-08-27 Magnetic resonance imaging pontine signal abnormality in neurological Wilson disease: A case report Gajurel, Bikram Prasad Karki, Susmin Parajuli, Asmita Khanal, Sunil Babu Clin Case Rep Case Report KEY CLINICAL MESSAGE: WD is diagnosed with the help of a brain MRI, which frequently reveals hyperintensities in the lentiform nucleus. But occasionally, high signals can be seen in the pons, thalamus, and midbrain. ABSTRACT: Wilson disease is a rare inherited disorder due to impaired copper excretion. The brain MRI mainly shows hyperintensities in the lentiform nucleus. We report the case of an 18 years old female diagnosed with neurological Wilson disease, presenting with uncommon brain MRI hyperintensities, predominantly in the pons, thalamus, and midbrain. John Wiley and Sons Inc. 2023-08-25 /pmc/articles/PMC10457478/ /pubmed/37636888 http://dx.doi.org/10.1002/ccr3.7851 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Gajurel, Bikram Prasad Karki, Susmin Parajuli, Asmita Khanal, Sunil Babu Magnetic resonance imaging pontine signal abnormality in neurological Wilson disease: A case report |
title | Magnetic resonance imaging pontine signal abnormality in neurological Wilson disease: A case report |
title_full | Magnetic resonance imaging pontine signal abnormality in neurological Wilson disease: A case report |
title_fullStr | Magnetic resonance imaging pontine signal abnormality in neurological Wilson disease: A case report |
title_full_unstemmed | Magnetic resonance imaging pontine signal abnormality in neurological Wilson disease: A case report |
title_short | Magnetic resonance imaging pontine signal abnormality in neurological Wilson disease: A case report |
title_sort | magnetic resonance imaging pontine signal abnormality in neurological wilson disease: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10457478/ https://www.ncbi.nlm.nih.gov/pubmed/37636888 http://dx.doi.org/10.1002/ccr3.7851 |
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