Primary hypothyroidism masquerading as hepatic encephalopathy: case report and review of the literature
- aUniversity of Cincinnati, Cincinnati, Ohio, USA: Department of Internal Medicine, bDivision of Digestive Diseases
- Dr Michael P Jones, Northwestern University School of Medicine, 251 East Huron Street, Galter Pavilion 4–104, Chicago, IL 60611–2908, USA (e-mail: mpjones{at}nmh.org)
- Received 30 July 1999
- Accepted 22 November 1999
Abstract
A 74 year old woman with hepatitis C of long duration was admitted to hospital in hyperammonaemic coma. Despite aggressive treatment of hepatic encephalopathy, there was no clinical improvement. As part of her evaluation for other causes of altered mental status, she was found to be profoundly hypothyroid. Treatment with thyroid replacement hormone was accompanied by prompt normalisation of her mental status and hyperammonaemia. Hypothyroidism may exacerbate hyperammonaemia and portosystemic encephalopathy in patients with otherwise well compensated liver disease. Hyopthyroidism should be considered in the differential diagnosis of encephalopathy in patients with liver disease.
