Hashimoto encephalopathy shares common clinical features with Creutzfeldt-Jakob disease and must be regarded as a differential diagnosis because of its good prognosis. We report a case of Hashimoto encephalopathy, which had not been recognized before the diagnosis of Creutzfeldt-Jakob disease. The electroclinical findings were compatible with probable Creutzfeldt-Jakob disease and coexistence of Hashimoto thyroiditis was supported by high titers of anti-thyroid microsomal antibody and cytopathologic findings. Hashimoto encephalopathy was not improved, which was most likely due to the coexistence of Creutzfeldt-Jakob disease.ope
Opsoclonus-myoclonus syndrome (OMS) is characterized by opsoclonus and arrhythmic myoclonic jerks pr...
Background :The mechanisms responsible for the disturbed hematopoiesis in myelodysplastic syndrome (...
Mondor's disease is a rare condition involving the breast and anterior chest wall and it is characte...
Semantic dementia is a rare, distinct form of frontotemporal lobar degeneration, characterized by a ...
Facial blushing is a personally disabling condition, which can result in emotional disturbance and b...
Xanthoma disseminatum is a rare mucocutaneous xanthomatosis classified as a benign form of non-Lange...
Limbic encephalitis has been reported usually as an autoimmune complication related to onconeuronal ...
Background: Epileptic nystagmus is rare. There is no report in Korea about epileptic nystagmus by th...
Indeterminate cell histiocytosis (ICH) is a rare proliferative disorder of indeterminate cells, whic...
Idiopathic avascular necrosis of the capitate is a very rare condition. Only 7 cases have been repor...
Carcinoid tumor of the middle ear cavity is a rare neoplasm of low malignant potential. It grows slo...
Essential hyperhidrosis is a socially disabling and emotionally embarrassing condition. Localized ex...
We report a 45-year-old woman presenting with a painful subungual epidermal cyst on the 4th finger n...
Myotonic dystrophy is the most common autosomal dominant myopathy in adults. It is a disorder with m...
Influenza virus has been reported to have various neurologic involvements, and it is known to be a p...
Opsoclonus-myoclonus syndrome (OMS) is characterized by opsoclonus and arrhythmic myoclonic jerks pr...
Background :The mechanisms responsible for the disturbed hematopoiesis in myelodysplastic syndrome (...
Mondor's disease is a rare condition involving the breast and anterior chest wall and it is characte...
Semantic dementia is a rare, distinct form of frontotemporal lobar degeneration, characterized by a ...
Facial blushing is a personally disabling condition, which can result in emotional disturbance and b...
Xanthoma disseminatum is a rare mucocutaneous xanthomatosis classified as a benign form of non-Lange...
Limbic encephalitis has been reported usually as an autoimmune complication related to onconeuronal ...
Background: Epileptic nystagmus is rare. There is no report in Korea about epileptic nystagmus by th...
Indeterminate cell histiocytosis (ICH) is a rare proliferative disorder of indeterminate cells, whic...
Idiopathic avascular necrosis of the capitate is a very rare condition. Only 7 cases have been repor...
Carcinoid tumor of the middle ear cavity is a rare neoplasm of low malignant potential. It grows slo...
Essential hyperhidrosis is a socially disabling and emotionally embarrassing condition. Localized ex...
We report a 45-year-old woman presenting with a painful subungual epidermal cyst on the 4th finger n...
Myotonic dystrophy is the most common autosomal dominant myopathy in adults. It is a disorder with m...
Influenza virus has been reported to have various neurologic involvements, and it is known to be a p...
Opsoclonus-myoclonus syndrome (OMS) is characterized by opsoclonus and arrhythmic myoclonic jerks pr...
Background :The mechanisms responsible for the disturbed hematopoiesis in myelodysplastic syndrome (...
Mondor's disease is a rare condition involving the breast and anterior chest wall and it is characte...