No abstract available.

No abstract available.
Animals ; Corrosion Casting* ; Corrosion* ; Head* ; Rats*

No abstract available.
Necrosis*

We observed clinical features of 18 bronchopulmonary dysplasia (BPD) patients who were admitted to the neonatal intensive care unit in the Severance Hospital of Yonsel University College of Medicine from January 1. 1987 to June 30. 1991. Eight patients in whom ventilator settings were unchanged for more than 5 days because of lack of improvement in pulmonary function. The effects of dexamethasone in ventilator-dependent were included in the short-term dexamethasone therapy. 1) Eighteen BPD patients consisted of 15 premature infants (83%), 1 full-term infant, and 2 post-term infants, The mean gestational age of the patients were 30 weeks and the mean birth weight was 1,420gm. And there were 13 male and 5 female infants. 2) The underlying conditions which necessitated ventilatory support support were hyaline membrane disease in 13 patients (72%), apnea in 2 (11%), and meconium aspiration syndrome in 3. There patients with meconium aspiration syndrome were either full-term or post-term infants, of whom 2 had neonatal persistent pulmonary hypertension. 3) The mean age at the start of ventilator care was 8 hours and the mean PIP was 32 cm H2O. The mean duration of ventilator care of oxygen therapy and of high O2 requirement (FiO2>0.8) were 39 days, 75 days and 20 days, respectively. 4) Patent ductus arteriosus developed in 8 patients during mechanical ventilation, but they were all closed with the use of mefenamic acid, There were also 4 cases of pneumothorax, 2 cases of pulmonary parenchymal emphysema, and 1 case each of pneumomediastinum and pneumoperitoneum. 5) The mean gestational age of the dexamethasone-treated group was 30 weeks and the mean birth weight was 1,320gm, The mean age at which dexamethasone therapy was started was 39 days after birth, and in only 3.3 days 6 patients were successfully weaned from ventilator, In 5 cases the first trial of dexamethasone therapy was enough but the rest needed the 2nd trial for ventilator weaning. 6) In 6 BPD patient who were weaned from the ventilator after dexamethasone therapy, there were significant decreases in MAP (11.1 vs 8.0 cmH2O), and FiO2 (0.73 vs 0.61), but a significant increase in the urine output (2.56 vs 3.7ml/kg/hr) for the pretreatment (5 days prior to therapy) versus posttreatment period (first day of therapy). 7) The complications of dexamethasone treatment were transient hypertension and hyperglycemia in 3 patients, and systemic candidiasis and gastrointestinal bleeding in 2 patients who failed to be weaned after dexamethasone therapy. Our results suggest that the short-term dexamethasone therapy in bronchopulmonary dysplasia patients who are dependent on mechanical ventilation enables weaning in a short period of time. The inspiratory oxygen concentration and the mean airway pressure may be decreased and the urine output may be increased from the first day of medication, improves pulmonary function and decreases pulmonary interstitial edema.
Apnea ; Birth Weight ; Bronchopulmonary Dysplasia* ; Candidiasis ; Dexamethasone* ; Ductus Arteriosus, Patent ; Edema ; Emphysema ; Female ; Gestational Age ; Hemorrhage ; Humans ; Hyaline Membrane Disease ; Hyperglycemia ; Hypertension ; Hypertension, Pulmonary ; Infant ; Infant, Newborn ; Infant, Premature ; Intensive Care, Neonatal ; Male ; Meconium Aspiration Syndrome ; Mediastinal Emphysema ; Mefenamic Acid ; Oxygen ; Parturition ; Pneumoperitoneum ; Pneumothorax ; Respiration, Artificial ; Ventilator Weaning ; Ventilators, Mechanical ; Weaning

No abstract available.
Glomerulonephritis, IGA* ; Immunoglobulin A*

No abstract available.
Cervix Uteri* ; Female

No abstract available.
Glomerulonephritis, IGA* ; Immunoglobulin A* ; Nephrotic Syndrome*

This study was undertaken to evaluate the clinical usefulness of magnetic evoked potentials(MEP) in localization of motor pathway lesions and the relation between motor weakness and MEP alterations. The patient group consisted of 50 patients(33 men and 17 women) with vanous diseases involving motor pathway, among which were 21 cerebral infarction, 15 intracerebrai hemorrhage, 3 cervical spondylosis, 3 amyotrophic lateral sclerosis and 8 peripheral polyneuropathy, confirmed by neurological findings, CT or MRI, EMG and nerve conduction velocity. The results were compared with 20 healthy subjects (11 men and 9 women) as a control group. MEP were recorded by using Digitimer magnetic stimulator model Dl90 and Medelec ER 94a/Sensor apparatuses, and MEP were evoked by magnetic stimulations over the vertex, the 7th cervical vertebra and Erb's point, and central motor conduction time (CMCT) was calculated by substracting the onset latency of abductor pollicis brevis muscle responses obtained by stimulation over the C7 vertebra from that obtained by stimulation over the scalp. The mean latencies of MEP after transcranial magnetic stimulations were prolonged in patients with motor pathway lesion, and mean CMCT were prolonged in patients with stroke. Cortical MEP were not elicited in stroke patients with profound motor weakn-ess below motor power 2/5 in arm, Prolongation of mean latency of cortical MEP and mean CMCT were correlated with motor weakness below motor power 4/5. In stroke patients, there were prolongation of mean CMCT and mean latency of cortical MEP evoked by stimulation to the undamaged hemisphere. These results suggest that magnetic MEP test is safe and useful in evaluation of motor pathway lesions.
Amyotrophic Lateral Sclerosis ; Arm ; Cerebral Infarction ; Evoked Potentials, Motor* ; Hemorrhage ; Humans ; Magnetic Resonance Imaging ; Male ; Neural Conduction ; Polyneuropathies ; Scalp ; Spine ; Spondylosis ; Stroke ; Transcranial Magnetic Stimulation

We herein describe a case of a 55-year-old healthy woman with localized primary thymic amyloidosis presented as a mediastinal mass, found incidentally by chest radiography. Computed tomography revealed a 4.1 cm soft tissue lesion with nodular calcification in the left anterior mediastinum. The resected specimen was a well-defined lobulating mass with calcification. Microscopically, the mass was consisted of amorphous eosinophilc hyalinized substances involving the thymus and intrathymic lymph nodes. These eosinophilic substances showed apple-green bi-refringence under polarized light after staining with Congo red. In immunohistochemical study, they were positive for kappa and lambda light chains and negative for amyloid A. There was no evidence of systemic amyloidosis in clinical investigations. A final diagnosis of localized primary thymic amyloidosis was made.
Amyloid ; Amyloidosis ; Congo Red ; Eosinophils ; Female ; Humans ; Hyalin ; Light ; Lymph Nodes ; Mediastinum ; Middle Aged ; Thorax ; Thymoma ; Thymus Gland

No abstract available.
Polycystic Kidney Diseases*