The effects of acute carbon monoxide poisoning on the hepatic blood flow were studied in mongrel dogs. In this study dogs were divided into two groups, namely control and experimental, and the hepatic blood flow measured by the determination of the fractional clearance of the intravenously administered colloid 198Au. In the experimental group carbon monoxide poisoning was induced by the rebreathing of about 2% CO gas mixture for 15 minutes, and the hepatic blood flow was measured before and 30 minutes after the completion of the rebreathing of the gas mixture. The hepatic blood flow in the experimental group showed a insignificant relative increase compared to that in the control group. The alteration of the mean value of the hepatic blood flow following carbon monoxide poisoning appeared proportionate to that of the cardiac index, and inversely proportionate to those of the femoral artery mean pressure and the total peripheral resistance. However, the individual value of hepatic blood flow revealed no correlation with any of these hemodynamic measurements.
Animals ; Carbon Monoxide Poisoning* ; Carbon Monoxide* ; Carbon* ; Colloids ; Dogs ; Femoral Artery ; Hemodynamics ; Vascular Resistance

No abstract available.
Heart Valve Diseases* ; Heart Valves* ; Heart*

No abstract available.
Esophageal Perforation*

No abstract available.
Esophageal Perforation*

Prader-Willi(PW)syndrome is characterized by obesity, hypotonia, mental retardation, hypogonadism, short stature, excessive eating and characteristic facial appearance. Diabetes mellitus has been considered a component of PW syndrome. Recently this syndrome is caused by the absence of paternally derived genes normally located on chromosome segment 15 q11-q13 or may be the result of maternal uniparental disomy with the absence of paternally derived 15 q11-q13 region. The developement of probes containing segments of DNA from chromosome region 15 q11-q13 provides the oppotunity to confirm the diagnosis of PW syndrome by fluorescence in situ hybridization(FISH). We experienced a 15-year-old boy of PW syndrome with diabetes mellitus, who revealed mental retardation, hypogonadism, obesity and microdeletion of chromosome 15 q11-q13 comfirmed by FISH.
Adolescent ; Chromosomes, Human, Pair 15* ; Diabetes Mellitus ; Diagnosis ; DNA ; Eating ; Fluorescence ; Humans ; Hypogonadism ; Intellectual Disability ; Male ; Muscle Hypotonia ; Obesity ; Prader-Willi Syndrome* ; Uniparental Disomy

Fifty-two cases of neurilemmoma, which occurred in the skin and soft tissue and filed at the Department of Clinical Pathology, Catholic University Medical College from 1974 to 1984, were included for the clinical study. Forty four cases whose microscopic slides were available were reviewed for the histopathologic observation. The results were as follows : Clinical observations 1) The average age of the patients was 42.8% years old, and the average duration of tlie tumor was 3.9 years. 2) Eight cases were acompanied with tenderness and cases with tingling sensation. Clinica] signs described prior to biopsy were palpable mass(15), slow growing mass (8), palpable cystic mass(6) and hard mass(4). 3) The mean diameter was 2.6m (0.45cm-8cm), and the frequent sites were head and neck (32.7%), upper extremities(28.8%), lower extremities (23.11%) and trunk (15.4%) in decreasing orders. Histopathologic observations 1) 33 cases were composed of both Antoni A and type B with variable composition, but only Antoni type A was observed in 6 cases and Antoni type B in 5 Cases. 2) On the areas of Antoni type B, there were several degenerative changes including cystic change (52.3%), hemorrhage(50%), hyalinization(27.3%), necrosis(25%), and calcification(4.5%). 3) In 3 cases out of 44, the tumor was observed in the dermis and the tumors composed of Antoni A only occurred on the tongue, neck, and upper arm.
Arm ; Biopsy ; Dermis ; Head ; Humans ; Lower Extremity ; Neck ; Neurilemmoma* ; Pathology, Clinical ; Sensation ; Skin ; Tongue

No abstract available.
Saphenous Vein*

No abstract available.
Pulmonary Atelectasis*

No abstract available.
Oncogene Proteins* ; Oncogenes* ; Teratocarcinoma*

No abstract available.
Leg* ; Skin*