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Case report: bipolar disorder as the first manifestation of CADASIL
BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited cerebrovascular disease, clinically characterized by variable manifestations of migraine, recurrent transient ischemic attack or lacunar strokes, cognitive decline, and mo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4080756/ https://www.ncbi.nlm.nih.gov/pubmed/24929957 http://dx.doi.org/10.1186/1471-244X-14-175 |
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author | Park, Soyeon Park, Boram Koh, Min Kyung Joo, Yeon Ho |
author_facet | Park, Soyeon Park, Boram Koh, Min Kyung Joo, Yeon Ho |
author_sort | Park, Soyeon |
collection | PubMed |
description | BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited cerebrovascular disease, clinically characterized by variable manifestations of migraine, recurrent transient ischemic attack or lacunar strokes, cognitive decline, and mood disturbances. However, manic episodes have rarely been documented as an initial symptom of CADASIL and bipolar disorder presenting as the first manifestation in CADASIL has not been reported previously from evaluations by psychiatrists or psychological testing by psychologists. CASE PRESENTATION: A 53 year old woman developed symptoms of mania in her 50s leading to a personality change involving a continuously labile mood and irritability over a number of years. Neuropsychological testing revealed an intact memory, but impairment in attention and executive function. In the Rorschach test, she showed a high level of cognitive rigidity. Magnetic resonance imaging findings were very consistent with a diagnosis of CADASIL, which was confirmed by genetic testing for NOTCH3 mutations. Atypical antipsychotics proved to be helpful in treating her manic symptoms and for behavior control. CONCLUSION: We present a novel case of CADASIL that first presented as bipolar disorder. We contend that when patients show a late onset personality change or chronically irritable mood that deteriorates over many years, an organic cause such as CADASIL must be considered. Further studies are needed to better understand the exact impacts of cerebral tissue lesions and psychiatric symptoms in CADASIL patients. |
format | Online Article Text |
id | pubmed-4080756 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40807562014-07-03 Case report: bipolar disorder as the first manifestation of CADASIL Park, Soyeon Park, Boram Koh, Min Kyung Joo, Yeon Ho BMC Psychiatry Case Report BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited cerebrovascular disease, clinically characterized by variable manifestations of migraine, recurrent transient ischemic attack or lacunar strokes, cognitive decline, and mood disturbances. However, manic episodes have rarely been documented as an initial symptom of CADASIL and bipolar disorder presenting as the first manifestation in CADASIL has not been reported previously from evaluations by psychiatrists or psychological testing by psychologists. CASE PRESENTATION: A 53 year old woman developed symptoms of mania in her 50s leading to a personality change involving a continuously labile mood and irritability over a number of years. Neuropsychological testing revealed an intact memory, but impairment in attention and executive function. In the Rorschach test, she showed a high level of cognitive rigidity. Magnetic resonance imaging findings were very consistent with a diagnosis of CADASIL, which was confirmed by genetic testing for NOTCH3 mutations. Atypical antipsychotics proved to be helpful in treating her manic symptoms and for behavior control. CONCLUSION: We present a novel case of CADASIL that first presented as bipolar disorder. We contend that when patients show a late onset personality change or chronically irritable mood that deteriorates over many years, an organic cause such as CADASIL must be considered. Further studies are needed to better understand the exact impacts of cerebral tissue lesions and psychiatric symptoms in CADASIL patients. BioMed Central 2014-06-14 /pmc/articles/PMC4080756/ /pubmed/24929957 http://dx.doi.org/10.1186/1471-244X-14-175 Text en Copyright © 2014 Park et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. |
spellingShingle | Case Report Park, Soyeon Park, Boram Koh, Min Kyung Joo, Yeon Ho Case report: bipolar disorder as the first manifestation of CADASIL |
title | Case report: bipolar disorder as the first manifestation of CADASIL |
title_full | Case report: bipolar disorder as the first manifestation of CADASIL |
title_fullStr | Case report: bipolar disorder as the first manifestation of CADASIL |
title_full_unstemmed | Case report: bipolar disorder as the first manifestation of CADASIL |
title_short | Case report: bipolar disorder as the first manifestation of CADASIL |
title_sort | case report: bipolar disorder as the first manifestation of cadasil |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4080756/ https://www.ncbi.nlm.nih.gov/pubmed/24929957 http://dx.doi.org/10.1186/1471-244X-14-175 |
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