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Involuntary crying episodes with Susac’s syndrome—a rare presentation of a rare disease: a case report
BACKGROUND: In this case, we reported the pseudobulbar affect (PBA) in a patient with Susac’s syndrome—a rare condition that was caused by a rare syndrome. Previous case reports of Susac syndrome described psychiatric symptoms such as emotional disturbances or personality changes. Only a few case re...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036746/ https://www.ncbi.nlm.nih.gov/pubmed/35468771 http://dx.doi.org/10.1186/s12883-022-02639-9 |
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author | Alshaqi, O. Moodie, T. Alchaki, A. |
author_facet | Alshaqi, O. Moodie, T. Alchaki, A. |
author_sort | Alshaqi, O. |
collection | PubMed |
description | BACKGROUND: In this case, we reported the pseudobulbar affect (PBA) in a patient with Susac’s syndrome—a rare condition that was caused by a rare syndrome. Previous case reports of Susac syndrome described psychiatric symptoms such as emotional disturbances or personality changes. Only a few case reports have reported psychiatric disorders in patients with Susac’s syndrome. There were no reported cases of Susac syndrome with PBA as an initial presentation. CASE PRESENTATION: Our patient was 56 years old and presented with involuntary crying, left-sided headache, left-sided hearing loss, and tinnitus. Brain MRI showed numerous areas of restricted diffusion and enhancement involving the corpus callosum, bilateral hemispheres, and brainstem. Ophthalmological evaluation showed bilateral branch retinal artery occlusion. She was diagnosed with Susac’s syndrome and PBA. She was treated with cyclophosphamide and dextromethorphan hydrobromide/quinidine sulfate with excellent recovery. This is a 2-year clinical course. DISCUSSION AND CONCLUSIONS: Recognition of the clinical presentation of Susac’s syndrome and PBA with early diagnosis and treatment are the keys to preventing further disability and impact on patients and their families. |
format | Online Article Text |
id | pubmed-9036746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-90367462022-04-26 Involuntary crying episodes with Susac’s syndrome—a rare presentation of a rare disease: a case report Alshaqi, O. Moodie, T. Alchaki, A. BMC Neurol Case Report BACKGROUND: In this case, we reported the pseudobulbar affect (PBA) in a patient with Susac’s syndrome—a rare condition that was caused by a rare syndrome. Previous case reports of Susac syndrome described psychiatric symptoms such as emotional disturbances or personality changes. Only a few case reports have reported psychiatric disorders in patients with Susac’s syndrome. There were no reported cases of Susac syndrome with PBA as an initial presentation. CASE PRESENTATION: Our patient was 56 years old and presented with involuntary crying, left-sided headache, left-sided hearing loss, and tinnitus. Brain MRI showed numerous areas of restricted diffusion and enhancement involving the corpus callosum, bilateral hemispheres, and brainstem. Ophthalmological evaluation showed bilateral branch retinal artery occlusion. She was diagnosed with Susac’s syndrome and PBA. She was treated with cyclophosphamide and dextromethorphan hydrobromide/quinidine sulfate with excellent recovery. This is a 2-year clinical course. DISCUSSION AND CONCLUSIONS: Recognition of the clinical presentation of Susac’s syndrome and PBA with early diagnosis and treatment are the keys to preventing further disability and impact on patients and their families. BioMed Central 2022-04-25 /pmc/articles/PMC9036746/ /pubmed/35468771 http://dx.doi.org/10.1186/s12883-022-02639-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Alshaqi, O. Moodie, T. Alchaki, A. Involuntary crying episodes with Susac’s syndrome—a rare presentation of a rare disease: a case report |
title | Involuntary crying episodes with Susac’s syndrome—a rare presentation of a rare disease: a case report |
title_full | Involuntary crying episodes with Susac’s syndrome—a rare presentation of a rare disease: a case report |
title_fullStr | Involuntary crying episodes with Susac’s syndrome—a rare presentation of a rare disease: a case report |
title_full_unstemmed | Involuntary crying episodes with Susac’s syndrome—a rare presentation of a rare disease: a case report |
title_short | Involuntary crying episodes with Susac’s syndrome—a rare presentation of a rare disease: a case report |
title_sort | involuntary crying episodes with susac’s syndrome—a rare presentation of a rare disease: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036746/ https://www.ncbi.nlm.nih.gov/pubmed/35468771 http://dx.doi.org/10.1186/s12883-022-02639-9 |
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