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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Main Authors: Fredy Nehme, MD, Salam Kadhem, MD, Rawaa Ebrahem, MD, Rami Mortada, MD
Format: Article
Language:English
Published: Elsevier 2018-01-01
Series:AACE Clinical Case Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2376060520304429
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spelling 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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