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정덕용 대한흉부심장혈관외과학회 1984 Journal of Chest Surgery (J Chest Surg) Vol.17 No.3
In this study, 213 cases of the spontaneous pneumothorax experienced at the department of thoracic and cardiovascular surgery, Chungnam National University Hospital during from April, 1977, till Dec, 1983 were reviewed. 1.Sex ratio of the studied patients was 7.19;1 showing high incidence male patients. The incidence according to the age group showed that 20.2%, 18.3% of the patients belong to the age group 6th, 5th decade respectively. 2.The etiologic factors were as follows, tuberculous origin in 50.2%, unknown origin in 28.2%, COPD in 3.3%, bullae in 8.5%. The site was right in 47.9% and left in 44.1%, bilateral in 8%. 3.The clinical symptoms were frequently dyspnea in 35%, chest pain in 27.5%. 4.The employed method of treatment were as follow, bed rest with oxygen inhalation in 1.9%, closed thoracostomy in 95.8%, open thoracotomy in 7.98%, which bullectomy was performed in 12 cases and pneumonectomy in 3 cases and lobectomy in 1 case and decortication with simple closure of bleb was performed in remaining 1 case. 5.The duration of closed thoracostomy was longer in tuberculosis, which average duration was 11.28 days. 6.The overall recurrent rate was 12.3%.
단독 선천성 심기형을 동반한 내장 완전 좌우 역위증 2례 보고 [
정덕용 대한흉부심장혈관외과학회 1985 Journal of Chest Surgery (J Chest Surg) Vol.18 No.4
Two cases of situs inversus totalis with isolated congenital heart disease were treated at department of cardiothoracic surgery, Chungnam National University Hospital. Sixteen months old girl was operated under diagnosis of PDA with mirro-image dextrocardia by triple ligation. Fifteen months old girl was managed under diagnosis of VSD with mirro-image dextrocardia by simple closure of VSD with extracorporeal circulation. The former had smooth postoperative course, but the latter was died of asphyxia due to vomitus on postoperative second day
Anatomically Corrected Malposition of the Great Arteries 1례 보고
정덕용 대한흉부심장혈관외과학회 1985 Journal of Chest Surgery (J Chest Surg) Vol.18 No.4
One case of anatomically corrected malposition of the great arteries was managed at department of cardiothoracic surgery, Chungnam National University Hospital at May, 1984. Anatomically corrected malposition of the great arteries was an extremely rare congenital heart disease. Only 21 cases were reported in English literatures. If there are no associated cardiac disease, the patient will have normal life span. This 39 year old man had suffered from exertional dyspnea for 6 years. He had carried out normal military service as a sergeant for 8 years, and his life was not restricted before this episode. He had operated under diagnosis of mitral stenoinsufficiency & tricuspid regurgitation but died because of lower cardiac output.,br> At autopsy, the great arteries were malpositioned but viscera and lung were normal position and picture. The aortic valve was located left and anterior to the pulmonic valve and there are bilateral conus in this anatomically corrected malposition of the great arteries. The coronary arteries were normal distribution.