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- 저자 : 채성수(Sung-Soo Chae) (검색결과 4 건)
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선경,최영호,채성수,김학제,김형묵,Sun, Kyung,Choi, Young-Ho,Chae, Sung-Soo,Kim, Hark-Jei,Kim, Hyong-Mook 대한흉부심장혈관외과학회 1982 Journal of Chest Surgery (J Chest Surg) Vol.15 No.4
A 45 year old male officer was admitted due to upper substernal pain for 1 month, which was aggravated by swallowing. On past and family history, there was no specific history except heavy drinking. Simple chest x-ray revealed no specific abnormal findings. Preoperative esophagofiberscopy and Barium study showed midesophageal diverticulum, pulsion type, at about 2 cm below the left main bronchus. The opening of the diverticulum was located at the left posterolateral aspect of esophagus. Midesophageal false diverticulum, measuring 2 x 2 x 1 .S cm in size, was noted at about 5 cm under the aortic arch protruding through a slit-like muscular defect. After inversion of diverticular sac, interrupted sutures with 3-0 silks were done on muscular defect site, and mediastinal pleura was reinforced on the lesion with interrupted sutures. On 4th postoperative day, esophagography revealed no diverticulum or stenosis. Also esophagofiberscopy showed smooth mucosal tag without disturbance of passage. On 14th postoperative day, the patient was discharged uneventfully, and follow-up for 3 months after discharge revealed nothing abnormal symptoms. The authors report one case of midesophageal, pulsion type, false diverticulum.
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선경,백광제,이철세,채성수,김학제,김형묵,Sun, Kyung,Baek, Kwang-Je,Lee, Chol-Sei,Chae, Sung-Soo,Kim, Hark-Jei,Kim, Hyung-Mook 대한흉부심장혈관외과학회 1984 Journal of Chest Surgery (J Chest Surg) Vol.17 No.1
Congenital Cystic Adenomatiod Malformation (C.C.A.M.) is rare, but one of the most common congenital pulmonary anomalies that cause acute respiratory distress in the newborn infants. It is characterized and differentiated from the diffuse pulmonary cystic disease pathologically, i.e. adenomatoid appearance due to marked proliferation of the terminal respiratory components. An 2/12 year old male patient was suffered from respiratory distress and cyanosis on crying since birth, but no specific therapy was given. With progression of symptoms, he came to Korea University Hospital for further evaluation and then transfered to Dept. of Chest Surgery for operative correction under the impression of Congenital Obstructive Emphysema suggested by a pediatrician. On gestational and family history, there was nothing to be concerned such as congenital anomaly. Physical examinations showed; moderate nourishment and development (Wt. 5.5kg), cyanosis on crying, both intercostal and lower sternal retraction on inspiration, Lt. chest building with tympany, Rt. shifting of cardiac dullness, decreased breathing sound with expiratory wheezing on entire Lt. lung field, decreased breathing sound on Rt. upper lung filed, and tachycardia. The remainders were nonspecific. Laboratory findings were normal except WBC $14000/mm^3$ (lymphocyte 70%), Hgb 9.8m%, Hct 28%, negative Mantaux test, and sinus tachycardia and counter-clockwise rotation on EKG. Preoperative simple Chest PA revealed marked hyperlucent entire Lt. lung, herniation of Lt. upper lobe to Rt., collapsed Rt. upper lobe, tracheal deviation and mediastinal shifting to Rt., and no pleural reaction. At operation, after Lt. posterolateral thoracotomy, 4th rib was resected. Operative findings were severe emphysematous changes limited to both lingular segmentectomy was done. The resected specimen showed slight solidity, measuring $8{\times}4.5{\times}2cm$ in size, and small multiple cystic spaces filled with air. Microscopically, entire tissue structures were glandular in appearance, cyst were lined by ciliated columnar epithelium, and occasional cartilages were noted around the cystic spaces. Bronchial elements were dilated but normal pattern on histologically. The patient had a good postoperative courses clinically and radiologically, and discharged on POD 10th without event. The authors report a case of Cogenital Cystic Adenomatoid Malformation (C.C.A.M.)
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이성주,구원모,문승철,김대식,이건,임창영,김창회,채성수,Lee, Sung-Joo,Koo, Won-Mo,Moon, Seong-Cheol,Kim, Dae-Sig,Lee, Gun,Lim, Chang-Young,Kim, Chang-Hoe,Chae, Sung-Soo 대한흉부심장혈관외과학회 1998 Journal of Chest Surgery (J Chest Surg) Vol.31 No.3
Sternal fractures, once thought of as an uncommon phenomenon, have occurred with an increasing frequency, paralleling the incidence of motor vehicle accidents. The tremendous force necessary to cause sternal fracture and this bone's prominent position overlying major intrathoracic and mediastinal structures, have important implications in the assessment and treatment of patients. This evaluation is based on the review of 72 patients of traumatic sternal fracture treated at the Department of Thoracic and Cardiovascular Surgery, Seoul Adventist Hospital during the last 4 years from March 1993 to February 1997. The frequency was 12.2% of nonpenetrating chest trauma and average age was 43.2 years old. Automobile accidents(84%) and sternal body fractures(95.8%) with anterior displacements(19.4%) was the most common cause and fracture site. Increase of cardiac isoenzymes was more frequent and higher in sternal fracture than chest contusion but there was no relationship between the time to take normalization of them and the mode of trauma. 예전에는 그리 흔하지 않았던 흉골 골절이 자동차 사고의 증가와 비례해서 그 빈도가 증가 추세에 있다. 흉골 골절을 유발할 정도의 과도한 충격이나 골절로 인한 골편부는 그 위치가 종격동이나 흉강안의 기관들 근처에서 발생하기 때문에 이러한 기관이 흉골 골절로 손상을 받지 않았는지 잘 평가하는 것은 치료하는 데 있어 매우 중요하다. 본 연구는 1993년 3월부터 1997년 2월까지 4년간 서울 위생병원 흉부외과에서 치료한 72명의 흉골 골절 환자를 대상으로 이루어졌다. 흉부 손상 중 흉골 골절의 빈도는 12.2%였고 환자의 평균연령은 43.2세였다. 자동차 사고(84%)와 흉골 체부 골절(95.8%)이 가장 흔한 골절 요인과 위치였고 골절 형태는 골단부 이탈(displacement)이나 교차(overriding)없이 골절만인 경우가 51명(70.8%)으로 가장 많았고 골단부의 이탈은 전방(anterior, 19.4%)이 후방(posterior, 5.6%)보\ulcorner 많았다. 흉부 좌상 환자(LDH:13%, CPK:14%, CK-MB:12.2%, CK-MB>6% of CPK:5.3%)보다 흉골 골절 환자(LDH:56.8%, CPK:66.6%, CK-MB:43.1%, CK-MB>6% of CPK:25.4%)와 흉골 골단부 이탈로 수술 받아야 했던 환자(LDH:76%, CPK:95%, CK-MB:38%, CK-MB>65% of CPK:33%)에서 심동위효소 증가의 빈도는 컸고, 심동위효소의 평균 수치도 높았다. 그러나 증가된 심동위효소의 수치가 정상화되는데 소요되는 시간은 흉부 좌상 환자와 흉골 골절 환자 사이에 별 차이가 없었다.
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