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Biomedical subjects

S Mitake

Publications and source records attributed to S Mitake.

48 records · Page 3Linked to original sources

Intracytoplasmic inclusion bodies of the thalamus and the substantia nigra, and Marinesco bodies in myotonic dystrophy: a quantitative morphological study.

Intracytoplasmic inclusion bodies of the thalamus and the substantia nigra, and Marinesco bodies have been studied in four patients with myotonic dystrophy (MyD), eight patients with other neurological diseases (control A), and eight patients without neurological diseases (control B). The percentages of the affected cells were calculated by dividing the number of neurons including intracytoplasmic inclusion bodies of the thalamus and the substantia nigra, and Marinesco bodies, by the total cell count in these respective regions. Statistical analyses were performed with regard to the frequency of these bodies by using Student's t test. There was a significantly higher incidence of intracytoplasmic inclusion bodies of the thalamus (13.2% versus 0.7%, P less than 0.001) and the substantia nigra (20.4% versus 2.7%, P less than 0.001), and Marinesco bodies (37.4% versus 4.1%, P less than 0.001) in patients with MyD than in controls A and B. From our observations, it is suggested that the presence with a high frequency, in combination, of these bodies is not an incidental finding but may have an intimate and important relationship with the pathogenesis of MyD, and may be a conspicuous and diagnostically important feature of MyD.

Adult↗

[An autopsy case of pallido-nigro-luysian atrophy associated with OPLL].

Clinical and neuropathological studies of a case of pallido-nigro-luysian atrophy with thalamic degeneration and ossification of the posterior longitudinal ligament (OPLL) is reported. The patient was a 72-year-old man, suffering from gait disturbance caused by OPLL for about 3 years. The clinical features were characterized by gradual development of disorientation in place, time and person, memory disturbance, vertical gaze palsy and rigidity of extremities. Dysarthria, dysphagia, bradykinesia, masked face and neck dystonia appeared at the advanced stage of his illness. There was no tremor or other involuntary movements. A clinical diagnosis of parkinsonism was suspected. The main neuropathological findings were neuronal loss and gliosis in globus pallidus, substantia nigra, subthalamic nucleus and thalamus. In addition, neuronal loss of the anterior horn of the cervical spinal cord due to compression by OPLL (C4-C7) was recognized. The neuropathological findings of the present case were consistent with systemic degenerative disorder of the nervous system affecting the pallido-nigro-luysian tract. This rare disorder should be considered in the differential diagnosis of parkinsonism in old people.

Aged↗

[Development of Alzheimer neurofibrillary changes in two autopsy cases of myotonic dystrophy].

Histopathological examination of two autopsy cases of myotonic dystrophy (MyD), a 65-year-old man (case 1) and a 61-year-old woman (case 2), revealed Alzheimer's neurofibrillary tangle (NFT) in the limbic system without concomitant presence of senile plaque as well as cavum septi pellucidi and thalamic inclusion body. The NFT were particularly abundant in the mesolimbic cortex. In addition to these, small traumatic scars were observed in the frontal lobe of case 1, who had clinically shown severe dementia. From these findings, it might be assumed that both premature aging and head trauma played an important role in the pathogenesis of NFT in these patients with MyD. The dementia of case 1 could be correlated well with abundance of NFT in the mesolimbic cortex.

Aged↗

[Repeated hyperglycemic hemichorea in a patient with venous angioma in the putamen].

We report a case of an 81-year-old diabetic woman who had three episodes of choreic involuntary movement in the left extremities. Brain CT revealed faintly increased density in the right putamen. On MRI performed 28 days after onset of the left hemichorea, the right putamen showed increased signal intensity on T1-weighted images and the so-called "medusa-like appearance" of medullary venous drainage into the thalamostriate vein on enhanced T1-weighted images. These findings indicated petechial hemorrhage of the right putamen from a venous angioma. We hypothesize that this hemorrhagic change due to a venous malformation in the basal ganglia may induce involuntary movements in diabetic patients during severe hyperglycemia.

Aged↗