https://doi.org/10.4081/reumatismo.2018.1090
Hashimoto’s encephalopathy in a patient with septal panniculitis: a case report
Submitted: 23 October 2017
Accepted: 2 July 2018
Published: 20 December 2018
Accepted: 2 July 2018
Abstract Views: 1015
PDF: 766
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All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Authors
Hashimoto’s encephalopathy (HE) is an autoimmune form of encephalopathy, associated with autoimmune thyroiditis. Its prevalence is estimated to be 2:100,000. HE is characterized by behavioral changes, mental confusion, dysarthria, ataxia, psychosis, paranoia, convulsions, hallucinations, headache and hyperthermia. Elevated thyroid antibodies are necessary for diagnosis and the disease responds dramatically to glucocorticoid therapy. We describe a patient with HE and panniculitis, an association reported twice in the literature.
How to Cite
Cosso, C., Ghio, M., & Cutolo, M. (2018). Hashimoto’s encephalopathy in a patient with septal panniculitis: a case report. Reumatismo, 70(4), 268–269. https://doi.org/10.4081/reumatismo.2018.1090
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