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encephalomalacia/hypoxie
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Renal impairment, hypertension and encephalomalacia in an infant surviving severe intra-uterine anoxia.
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[Morphological substrates in the perinatal anoxia syndrome. Intra-alveolar hemorrhage and hyaline membranes of the lung, multiple stomach ulcers, bilateral kidney cortex necroses and periventricular encephalomalacia in a newborn infant].
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Cardiopulmonary hypoxemia encephalomalacia.
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[Multicystic encephalomalacia in an adult--a case report].
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A case of multicystic encephalomalacia found in adult life was described. A 35-year-old man was admitted to our hospital with a chief complaint of unsteadiness. He had developed normally until he fell into the shock state induced by mismatch blood transfusion at the age of 15 months. Since then he
Cerebral, renal and splenic lesions due to fetal anoxia and their relationship to malformations.
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Two newborn infants who suffered severe intra-uterine anoxia a few weeks before birth are described. Both died shortly after being born spontaneously and slightly prematurely. In one case the mother had attempted suicide by inhaling butane. The infant's kidneys were hypoplastic and resembled those
[Multicystic encephalomalacia. Review of 19 cases].
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OBJECTIVE
Multicystic encephalomalacia (EMQ) is a pediatric entity where the brain tissue is substituted by cavities of variably sizes.
METHODS
Nineteen children diagnosed of EMQ were studied retrospectively. We analyzed the etiology, diagnosis and the clinical and radiological
Multicystic encephalomalacia: CT appearance and pathological correlation.
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Perinatal insults, including anoxia, may lead to a form of cerebral necrosis designated multicystic encephalomalacia. This common condition is characterized by (a) moderate atrophic ventricular dilatation, (b) intact ventricular walls with thickened subependymal glial layer, (c) multiple cysts of
[Multicystic encephalomalacia in a surviving twin after death of the other twin in utero].
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A case of multicystic encephalomalacia in a twin is reported. The other twin died in utero at 32 weeks gestational age. Because there was no evidence of fetal distress the pregnancy was allowed to continue until 36 weeks gestational age. Injuries to the surviving twin due to disseminated
A distinct clinicopathological variant of focal cortical dysplasia IIId characterized by loss of layer 4 in the occipital lobe in 12 children with remote hypoxic-ischemic injury.
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In 2011, the International League Against Epilepsy (ILAE) proposed a consensus classification system of focal cortical dysplasia (FCD) to distinguish clinicopathological subtypes, for example, "isolated" FCD type Ia-c and IIa-b, versus "associated" FCD type IIIa-d. The histopathological
Intracranial calcification in the infant and neonate: evaluation by sonography and CT.
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This study reports the sonographic and computed tomography (CT) findings in seven infants and neonates with intracranial calcifications and a spectrum of underlying disorders, including toxoplasmosis, cytomegalic inclusion disease, transverse/straight sinus thrombosis, and probable anoxia.
[Diagnoses to consider in newborn infants with inactive EEG tracings].
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Thirty-one neonates without any electroencephalographic activity detectable on the first EEG before day 5 were studied. In the first group (20 neonates) the first EEG was performed on day 0. Signs of foetal and/or perinatal anoxia were observed. In the second group (11 neonates), the first EEG was
[Neonatal ultrasonographic cerebral findings: association with risk factor for cerebral palsy].
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BACKGROUND
Is it possible to identify patients with cerebral palsy (CP) with postnatal ultrasound scan? Which risk factors are associated with an increased risk of CP?.
METHODS
The data of 37 children with CP, who were sonographically investigated during the first 24 hours of life were analyzed
CT findings in neonatal hypothermia.
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BACKGROUND
Newborn infants are particularly prone to hypothermia, a condition with a high mortality.
OBJECTIVE
To study the CT brain patterns in infants with hypothermia and neurological symptoms.
METHODS
We reviewed the brain CT of nine infants with neonatal hypothermia, multiple organ failure,
Late neuropathological consequences of strangulation.
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A case of a young man who was a victim of strangulation is presented. He arrived at the hospital in refractory status epilepticus, controlled only with intravenous pentobarbital. The initial CT scan showed mild cortical edema. Two days later, a CT scan showed diffuse cortical swelling and bilateral
Cognitive impairment in children with hemoglobin SS sickle cell disease: relationship to MR imaging findings and hematocrit.
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OBJECTIVE
Children with hemoglobin SS sickle cell disease are known to suffer cognitive impairment if they have silent infarct, but recent evidence suggests that patients with hemoglobin SS sickle cell disease may be impaired even if they are free of infarction. We test a hypothesis that cognitive
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