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encephalomalacia/asthénie
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[Sporadic abdominal pain, sensation of bloating, shortness of breath, tachycardia and weakness of the right side (ECG and thoracic radiography): (upper mesenteric embolism, mitral valve stenosis, infarction of the right kidney and encephalomalacia)].
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Nutritional encephalomalacia in turkeys: diagnosis and growth performance.
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An outbreak of neurological disease in 2 1/2-to-3 1/2-week-old male turkey poults was diagnosed morphologically as nutritional encephalomalacia. About 20 to 30% of the flock of 6360 showed clinical signs, which included going down with legs extended or hock-sitting and inability to get up,
Encephalomalacia associated with vitamin E deficiency in commercially raised emus.
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Thirteen of 64 emus on a commercial emu farm in Ohio exhibited neurological signs that included backward staggering, incoordination, generalized weakness, and sitting on their hocks with head retracted backward. Eight of the birds showing such signs were found dead. Two of these emus were
Severe neurologic involvement of Degos disease in a pediatric patient.
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A 14-year-old male presented with paresthesias on the right upper and lower extremities, headache, and vomiting. In addition to worsening paresthesia and weakness on the right side of his body, blurred vision, fever, and skin lesions developed. He also had skin lesions characterized with 3-10 mm
Long-term Outcome of Motor Function in a Child with Moyamoya Disease: A Case Report.
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[Purpose] This observational study provides a retrospective description of changes in motor function of a 10 year old child who suffered from motor weakness caused by Moyamoya disease (MMD) over an approximately 3 year follow-up observation period. [Methods] The child was diagnosed as MMD due to
Acute and chronic brain infarcts on MR imaging in a 20-year-old woman with acute posterior multifocal placoid pigment epitheliopathy.
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A 20-year-old woman recently diagnosed with acute posterior multifocal placoid pigment epitheliopathy developed headaches, weakness, and paresthesias. MR imaging of the brain revealed an acute infarct (demonstrated by diffusion-weighted images) in the head of the right caudate nucleus, a chronic
Diffusion tensor magnetic resonance imaging of microstructural abnormalities in children with brain injury.
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We present two pediatric cases demonstrating that diffusion tensor imaging is more efficient at revealing microstructural abnormalities of the brain than conventional magnetic resonance imaging because it enables measurements of the directionality and integrity of white matter fiber tracts. One
Encephalomalacic dysplastic mass lesion associated with vascular abnormalities in an elderly man. Is this "acquired" focal cortical dysplasia?
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Focal cortical dysplasia (FCD) is known to occur in association with a principal lesion and has been newly introduced as FCD type III in the ILAE 2011 classification system of FCDs. FCD type IIIc is associated with vascular malformations, and in all such cases in the literature with histologic
Surgical management of medically refractory epilepsy due to early childhood stroke.
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OBJECT.: The risk of developing epilepsy after perinatal stroke, hypoxic/ischemic injury, and intracerebral hemorrhage is significant, and seizures may become medically refractory in approximately 25% of these patients. Surgical management can be difficult due to multilobar or bilateral cortical
Acquired Hemicerebral Atrophy Secondary to Chronic Internal Carotid Steno-Occlusive Disease: A Case Series.
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Cerebral atrophy is a common finding in elderly patients; however, cerebrovascular disease causing progressive focal cerebral atrophy and dysfunction is unusual. In this report, we present 3 cases of hemicerebral atrophy due to ipsilateral internal carotid artery (ICA) stenosis or occlusion
Hemispherotomy for intractable epilepsy.
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BACKGROUND
Hemispherotomy is a surgical procedure for hemispheric disconnection. It is a technically demanding surgery. Our experience is presented here.
OBJECTIVE
To validate and compare the two techniques for hemispherotomy performed in patients with intractable epilepsies.
METHODS
A retrospective
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