A 76-year-old woman was admitted to our hospital because of repeated transient ischemic attacks (TIAs). Physical examinations showed hypertension and hepatosplenomegaly. Neurological examination revealed right hand pronation sign, right everted foot and slight right hemisensory disturbance.
Peripheral blood showed as follows : RBC 6.53×10
6/mm
3, Hb 18.2 g/dl, Ht 56.0%, WBC 10500/mm
3 and platelets 81.3×10
4/mm
3. Bone marrow examination showed hyperplasia involving all three marrow elements. Total red cell volume measured by the
51Cr method, was 63 ml/kg body weight. Serum vitamin B
12 was 3590 pg/ml and unsaturated B
12 binding capacity was 2559 pg/ml. Arterial oxygen saturation was 94.6%. High blood viscosity and platelet hyperaggregability were observed.
CT scan of the brain showed periventricular lucency. Magnetic resonance imaging (MRI) using T
2 weighted spine echo image demonstrated multiple high intensity areas located in basal ganglia and near the lateral ventricles. Positron emission tomography (PET) showed decreasement of regional cerebral blood flow and regional cerebral metabolic rate of O
2 in sites from left frontal lobe to left temporal lobe. Left carotid angiography showed a severe stenosis of M
1 portion.
On the basis of the findings, the diagnosis of polycythemia vera with TIAs was made. Although she was treated with ticlopidine, venesection or warfarin, TIAs occured repeatedly. Busulfan (2-4 mg/day given orally) and aspirin administration were effective to prevent TIAs. Therefore, the severe stenosis of M
1 portion of left carotid artery and platelet hyperaggregability contributed to TIAs in this case.
View full abstract