Palatal-Myoclonus as a Presentation of Hashimoto Encephalopathy: an interesting case report.
Objective: Hashimoto encephalopathy (HE) is known as a steroid-responsive encephalopathy associated with autoimmune thyroiditis or nonvascular inflammation-related autoimmune meningoencephalitis. The average age of onset of HE is approximately 50 years; and it is more common in women. The onset of H...
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Format: | Article |
Language: | English |
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Tehran University of Medical Sciences
2013-09-01
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Series: | Iranian Journal of Psychiatry |
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Online Access: | https://ijps.tums.ac.ir/index.php/ijps/article/view/119 |
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author | Esmaeel Ghoreishi Gholam Ali Shahidi Mohammad Rohani Mohammad Nabavi Mahbubeh Aghaei Fahimeh Haji Akhoundi |
author_facet | Esmaeel Ghoreishi Gholam Ali Shahidi Mohammad Rohani Mohammad Nabavi Mahbubeh Aghaei Fahimeh Haji Akhoundi |
author_sort | Esmaeel Ghoreishi |
collection | DOAJ |
description | Objective: Hashimoto encephalopathy (HE) is known as a steroid-responsive encephalopathy associated with autoimmune thyroiditis or nonvascular inflammation-related autoimmune meningoencephalitis. The average age of onset of HE is approximately 50 years; and it is more common in women. The onset of HE may be acute or subacute. The course of most HE cases is relapsing and remitting, which is similar to that of vasculitis and stroke.
Methods: In this article, we present a previously healthy 32 years old; veterinarian male with palatal myoclonus, as a rare presentation of this disorder, and review the neurologic aspects of hashimoto encephalitis .
Results: The clinical presentation of HE is characterized by progressive cognitive decline tremor, transient aphasia, seizures, abnormal gait, sleep disorder and stroke-like episodes . Myoclonus, either generalized or multifocal, and tremor, often of the bilateral upper extremities, is the most frequently observed involuntary movements in HE.
Conclusion: The rapidly progressive cognitive dysfunction and encephalopathies observed. |
first_indexed | 2024-12-20T16:15:53Z |
format | Article |
id | doaj.art-67f9d7cc05164838a150b8b1160525ee |
institution | Directory Open Access Journal |
issn | 1735-4587 2008-2215 |
language | English |
last_indexed | 2024-12-20T16:15:53Z |
publishDate | 2013-09-01 |
publisher | Tehran University of Medical Sciences |
record_format | Article |
series | Iranian Journal of Psychiatry |
spelling | doaj.art-67f9d7cc05164838a150b8b1160525ee2022-12-21T19:33:49ZengTehran University of Medical SciencesIranian Journal of Psychiatry1735-45872008-22152013-09-0183Palatal-Myoclonus as a Presentation of Hashimoto Encephalopathy: an interesting case report.Esmaeel Ghoreishi0Gholam Ali Shahidi1Mohammad Rohani2Mohammad Nabavi3Mahbubeh Aghaei4Fahimeh Haji Akhoundi5Department of Neurology, Ardebil University of Medical Sciences, Ardebil, IranDepartment of Neurology, Iran University of Medical Sciences, Tehran, IranDepartment of Neurology, Iran University of Medical Sciences, Tehran, IranDepartment of Allergy and Immunology, Iran University of Medical Sciences, Tehran, IranIran University of Medical Sciences, Tehran, IranIran University of Medical Sciences, Tehran, IranObjective: Hashimoto encephalopathy (HE) is known as a steroid-responsive encephalopathy associated with autoimmune thyroiditis or nonvascular inflammation-related autoimmune meningoencephalitis. The average age of onset of HE is approximately 50 years; and it is more common in women. The onset of HE may be acute or subacute. The course of most HE cases is relapsing and remitting, which is similar to that of vasculitis and stroke. Methods: In this article, we present a previously healthy 32 years old; veterinarian male with palatal myoclonus, as a rare presentation of this disorder, and review the neurologic aspects of hashimoto encephalitis . Results: The clinical presentation of HE is characterized by progressive cognitive decline tremor, transient aphasia, seizures, abnormal gait, sleep disorder and stroke-like episodes . Myoclonus, either generalized or multifocal, and tremor, often of the bilateral upper extremities, is the most frequently observed involuntary movements in HE. Conclusion: The rapidly progressive cognitive dysfunction and encephalopathies observed.https://ijps.tums.ac.ir/index.php/ijps/article/view/119Hashimoto encephalopathyabnormal movementpalatal myoclonus |
spellingShingle | Esmaeel Ghoreishi Gholam Ali Shahidi Mohammad Rohani Mohammad Nabavi Mahbubeh Aghaei Fahimeh Haji Akhoundi Palatal-Myoclonus as a Presentation of Hashimoto Encephalopathy: an interesting case report. Iranian Journal of Psychiatry Hashimoto encephalopathy abnormal movement palatal myoclonus |
title | Palatal-Myoclonus as a Presentation of Hashimoto Encephalopathy: an interesting case report. |
title_full | Palatal-Myoclonus as a Presentation of Hashimoto Encephalopathy: an interesting case report. |
title_fullStr | Palatal-Myoclonus as a Presentation of Hashimoto Encephalopathy: an interesting case report. |
title_full_unstemmed | Palatal-Myoclonus as a Presentation of Hashimoto Encephalopathy: an interesting case report. |
title_short | Palatal-Myoclonus as a Presentation of Hashimoto Encephalopathy: an interesting case report. |
title_sort | palatal myoclonus as a presentation of hashimoto encephalopathy an interesting case report |
topic | Hashimoto encephalopathy abnormal movement palatal myoclonus |
url | https://ijps.tums.ac.ir/index.php/ijps/article/view/119 |
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