Spontaneous Resolution of Postpartum Hashimoto Encephalopathy with Levothyroxine Therapy Alone
ABSTRACT: Objective: Hashimoto encephalopathy (HE) is an uncommon syndrome characterized by seizures, movement disorders, cognitive or neuropsychiatric symptoms associated with dysthyroidism, and elevated anti-thyroperoxidase antibodies. It is more prevalent in females and all age groups can be affe...
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doaj-fb77f60005dd47328e96972b0472059c2021-04-30T07:24:42ZengElsevierAACE Clinical Case Reports2376-06052018-01-01411315Spontaneous Resolution of Postpartum Hashimoto Encephalopathy with Levothyroxine Therapy AloneFredy Nehme, MD0Salam Kadhem, MD1Rawaa Ebrahem, MD2Rami Mortada, MD3Department of Internal Medicine, Kansas University School of Medicine, Wichita, Kansas; Address correspondence to Dr. Fredy Nehme, Department of Internal Medicine, Kansas University School of Medicine, 1010 North Kansas Street, Wichita, KS 67214.Department of Internal Medicine, Kansas University School of Medicine, Wichita, KansasDepartment of Internal Medicine, Kansas University School of Medicine, Wichita, KansasDepartment of Endocrinology, Kansas University School of Medicine, Wichita, Kansas.ABSTRACT: Objective: Hashimoto encephalopathy (HE) is an uncommon syndrome characterized by seizures, movement disorders, cognitive or neuropsychiatric symptoms associated with dysthyroidism, and elevated anti-thyroperoxidase antibodies. It is more prevalent in females and all age groups can be affected. While its pathophysiology remains unclear, it is commonly defined as a steroid-responsive condition. Rarely, HE manifests with cerebellar ataxia.Methods: We report the case of a 21-year-old female presenting with cerebellar HE after delivery spontaneously resolving without corticosteroid treatment.Results: This case adds to the limited data available on HE and challenges the common conception of HE as a steroid-responsive disease.Conclusion: While our case suggests that HE might spontaneously recover, it is too limited to be conclusive and further studies are needed to clearly define the mechanism, exacerbating factors, and treatment options. HE should be considered in patients with otherwise unexplained cerebellar ataxia.Abbreviations: HE Hashimoto encephalopathy; TPO Abs anti-thyroperoxidase antibodieshttp://www.sciencedirect.com/science/article/pii/S2376060520304429 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Fredy Nehme, MD Salam Kadhem, MD Rawaa Ebrahem, MD Rami Mortada, MD |
spellingShingle |
Fredy Nehme, MD Salam Kadhem, MD Rawaa Ebrahem, MD Rami Mortada, MD Spontaneous Resolution of Postpartum Hashimoto Encephalopathy with Levothyroxine Therapy Alone AACE Clinical Case Reports |
author_facet |
Fredy Nehme, MD Salam Kadhem, MD Rawaa Ebrahem, MD Rami Mortada, MD |
author_sort |
Fredy Nehme, MD |
title |
Spontaneous Resolution of Postpartum Hashimoto Encephalopathy with Levothyroxine Therapy Alone |
title_short |
Spontaneous Resolution of Postpartum Hashimoto Encephalopathy with Levothyroxine Therapy Alone |
title_full |
Spontaneous Resolution of Postpartum Hashimoto Encephalopathy with Levothyroxine Therapy Alone |
title_fullStr |
Spontaneous Resolution of Postpartum Hashimoto Encephalopathy with Levothyroxine Therapy Alone |
title_full_unstemmed |
Spontaneous Resolution of Postpartum Hashimoto Encephalopathy with Levothyroxine Therapy Alone |
title_sort |
spontaneous resolution of postpartum hashimoto encephalopathy with levothyroxine therapy alone |
publisher |
Elsevier |
series |
AACE Clinical Case Reports |
issn |
2376-0605 |
publishDate |
2018-01-01 |
description |
ABSTRACT: Objective: Hashimoto encephalopathy (HE) is an uncommon syndrome characterized by seizures, movement disorders, cognitive or neuropsychiatric symptoms associated with dysthyroidism, and elevated anti-thyroperoxidase antibodies. It is more prevalent in females and all age groups can be affected. While its pathophysiology remains unclear, it is commonly defined as a steroid-responsive condition. Rarely, HE manifests with cerebellar ataxia.Methods: We report the case of a 21-year-old female presenting with cerebellar HE after delivery spontaneously resolving without corticosteroid treatment.Results: This case adds to the limited data available on HE and challenges the common conception of HE as a steroid-responsive disease.Conclusion: While our case suggests that HE might spontaneously recover, it is too limited to be conclusive and further studies are needed to clearly define the mechanism, exacerbating factors, and treatment options. HE should be considered in patients with otherwise unexplained cerebellar ataxia.Abbreviations: HE Hashimoto encephalopathy; TPO Abs anti-thyroperoxidase antibodies |
url |
http://www.sciencedirect.com/science/article/pii/S2376060520304429 |
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