| Literature DB >> 21709844 |
Chai Soon Ngiu1, Norlinah M Ibrahim, Wan Nur Nafisah Wan Yahya, Hui Jan Tan, Norlaila Mustafa, Hamidon Basri, Raymond Azman Ali.
Abstract
Hashimoto encephalopathy (HE) is a poorly recognised steroid-responsive encephalopathy, with prominent neuropsychiatric features. Diagnosis is often difficult due to its heterogeneous clinical presentation, especially since the thyroid status or anti-thyroid antibody titres may not be related to the disease state. Here, the case of a 23-year-old Malay woman with Graves disease who presented with progressive encephalopathy diagnosed as HE is presented. She responded dramatically to high dose intravenous and then oral corticosteroid. A month after the initiation of treatment, she regained full independency.Entities:
Year: 2009 PMID: 21709844 PMCID: PMC3027930 DOI: 10.1136/bcr.01.2009.1501
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X