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1.
Journal of the Korean Neurological Association ; : 111-114, 2013.
Article in Korean | WPRIM | ID: wpr-162904

ABSTRACT

Cerebral venous thrombosis (CVT) is quite rare and underlying risk factors are diverse. We describe that 60-year-old man developed CVT after use of cyclosporine. He had suffered from leukocytoclastic vasculitis and urticarial vasculitis. Initial MR venogram revealed thrombosis in superior sagittal sinus, right transverse sinus and sigmoid sinus with multiple cortical and deep collateral veins. Anticoagulation was started and maintained for one year, then follow up MR venogram was normal. We suggest that cyclosporine might increase a risk of CVT.


Subject(s)
Colon, Sigmoid , Cyclosporine , Follow-Up Studies , Risk Factors , Superior Sagittal Sinus , Thrombosis , Vasculitis , Vasculitis, Leukocytoclastic, Cutaneous , Veins , Venous Thrombosis
2.
Journal of the Korean Neurological Association ; : 183-185, 2013.
Article in Korean | WPRIM | ID: wpr-135484

ABSTRACT

Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is one of the mitochondrial disorders that can present as a stroke-like episode or seizure. Although the pathophysiology of MELAS remains inconclusive, the main possibilities are thus far thought to be mitochondrial cytopathy and angiopathy. This case report describes a 61-year-old woman diagnosed with MELAS who presented simultaneously with vascular hyperemia and crossed cerebellar diaschisis.


Subject(s)
Female , Humans , Acidosis, Lactic , Hyperemia , Kearns-Sayre Syndrome , Mitochondrial Diseases , Mitochondrial Encephalomyopathies , Mitochondrial Myopathies , Seizures
3.
Journal of the Korean Neurological Association ; : 183-185, 2013.
Article in Korean | WPRIM | ID: wpr-135481

ABSTRACT

Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is one of the mitochondrial disorders that can present as a stroke-like episode or seizure. Although the pathophysiology of MELAS remains inconclusive, the main possibilities are thus far thought to be mitochondrial cytopathy and angiopathy. This case report describes a 61-year-old woman diagnosed with MELAS who presented simultaneously with vascular hyperemia and crossed cerebellar diaschisis.


Subject(s)
Female , Humans , Acidosis, Lactic , Hyperemia , Kearns-Sayre Syndrome , Mitochondrial Diseases , Mitochondrial Encephalomyopathies , Mitochondrial Myopathies , Seizures
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