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Multiple system atrophy with oculomotor abnormalities as a prominent manifestation: A case series
Multiple system atrophy (MSA) is a group of adult-onset sporadic neurodegenerative diseases, mainly classified as MSA-C and MSA-P types. Due to the diversity of clinical symptoms, diagnosis faces a significant challenge. In the present case, we report a patient with isolated vertigo as the first pre...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10289487/ https://www.ncbi.nlm.nih.gov/pubmed/37352034 http://dx.doi.org/10.1097/MD.0000000000034008 |
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author | Wei, Yuanxiao Chen, Ju Lu, Cancan Jiang, Yijing Liu, Zhiqiang Zhang, Wenzhao Fang, Liqun |
author_facet | Wei, Yuanxiao Chen, Ju Lu, Cancan Jiang, Yijing Liu, Zhiqiang Zhang, Wenzhao Fang, Liqun |
author_sort | Wei, Yuanxiao |
collection | PubMed |
description | Multiple system atrophy (MSA) is a group of adult-onset sporadic neurodegenerative diseases, mainly classified as MSA-C and MSA-P types. Due to the diversity of clinical symptoms, diagnosis faces a significant challenge. In the present case, we report a patient with isolated vertigo as the first presentation and abnormalities of the oculomotor system as the characteristic manifestations. CASE CONCERN: A 64-year-old male had dizziness for 1 year, aggravated for 4 months, with accompanying symptoms of unsteady walking. Physical examination revealed spontaneous nystagmus, abnormal ataxic movements, and a broad basal gait. Video nystagmography revealed saccade intrusions and macrosaccadic oscillations, and opsoclonus. Magnetic resonance imaging (MRI) was unremarkable early, and positron emission tomography-computed tomography (PET-CT) announced a reduction in the volume of the cerebellum and brainstem. DIAGNOSIS: The diagnosis of the possibility of MSA type-C, peripheral neuropathy, hypertension, and lacunar cerebral infarction was performed. CONCLUSION: Atypical early clinical presentation may lead to delays, and identifying the critical problem through the patient simple clinical status requires long-term clinical experience and various ancillary examination tools. |
format | Online Article Text |
id | pubmed-10289487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-102894872023-06-24 Multiple system atrophy with oculomotor abnormalities as a prominent manifestation: A case series Wei, Yuanxiao Chen, Ju Lu, Cancan Jiang, Yijing Liu, Zhiqiang Zhang, Wenzhao Fang, Liqun Medicine (Baltimore) 5300 Multiple system atrophy (MSA) is a group of adult-onset sporadic neurodegenerative diseases, mainly classified as MSA-C and MSA-P types. Due to the diversity of clinical symptoms, diagnosis faces a significant challenge. In the present case, we report a patient with isolated vertigo as the first presentation and abnormalities of the oculomotor system as the characteristic manifestations. CASE CONCERN: A 64-year-old male had dizziness for 1 year, aggravated for 4 months, with accompanying symptoms of unsteady walking. Physical examination revealed spontaneous nystagmus, abnormal ataxic movements, and a broad basal gait. Video nystagmography revealed saccade intrusions and macrosaccadic oscillations, and opsoclonus. Magnetic resonance imaging (MRI) was unremarkable early, and positron emission tomography-computed tomography (PET-CT) announced a reduction in the volume of the cerebellum and brainstem. DIAGNOSIS: The diagnosis of the possibility of MSA type-C, peripheral neuropathy, hypertension, and lacunar cerebral infarction was performed. CONCLUSION: Atypical early clinical presentation may lead to delays, and identifying the critical problem through the patient simple clinical status requires long-term clinical experience and various ancillary examination tools. Lippincott Williams & Wilkins 2023-06-23 /pmc/articles/PMC10289487/ /pubmed/37352034 http://dx.doi.org/10.1097/MD.0000000000034008 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | 5300 Wei, Yuanxiao Chen, Ju Lu, Cancan Jiang, Yijing Liu, Zhiqiang Zhang, Wenzhao Fang, Liqun Multiple system atrophy with oculomotor abnormalities as a prominent manifestation: A case series |
title | Multiple system atrophy with oculomotor abnormalities as a prominent manifestation: A case series |
title_full | Multiple system atrophy with oculomotor abnormalities as a prominent manifestation: A case series |
title_fullStr | Multiple system atrophy with oculomotor abnormalities as a prominent manifestation: A case series |
title_full_unstemmed | Multiple system atrophy with oculomotor abnormalities as a prominent manifestation: A case series |
title_short | Multiple system atrophy with oculomotor abnormalities as a prominent manifestation: A case series |
title_sort | multiple system atrophy with oculomotor abnormalities as a prominent manifestation: a case series |
topic | 5300 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10289487/ https://www.ncbi.nlm.nih.gov/pubmed/37352034 http://dx.doi.org/10.1097/MD.0000000000034008 |
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