• 제목/요약/키워드: Thoracic defect

검색결과 720건 처리시간 0.018초

방실중격결손증의 외과적 치료 (Surgical Treatment of Atrioventricular Septal Defect)

  • 이광숙
    • Journal of Chest Surgery
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    • 제22권6호
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    • pp.990-995
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    • 1989
  • Since 1984, 24 patients underwent repair of atrioventricular septal defect. Nineteen had a partial defect and 5 had a complete atrioventricular septal defect. There were 9 men and 15 women, ranging in age from 1 to 50 years [mean age, 13.3 years]. Four patients had a Downs syndrome. Additional congenital heart defects were present in 11 patients. One patient had palliative operation prior to total correction. In partial defects, the primum atrial septal defect was closed with Xenomedica patch and the mitral valve was repaired with simple closure of the septal commissure. Central incompetence from annular dilatation was repaired by a local annuloplasty. In complete defect, the septal defects were closed with two patches except one. Operative mortality was 5% in partial defects and 60% in complete defects and low cardiac output was the commonest etiology. In a mean follow-up period of 27.9 months [range, 4 to 63 months] there were no late death and no instances of late-onset complete heart block. One patient required reoperation [MVR] for residual mitral regurgitation. The majority of patients were asymptomatic and mean postop. NYHA functional class was 1.2.

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좌우단락을 보인 심방중격결손, 심실중격결손 및 동맥관개존을 동반한 폐동맥판막협착증 -1례 보고- (Pulmonary valvular stenosis combined with atrial septal defect, ventricular septal defect and patent ductus arteriosus with left to right shunt: a case report)

  • 정황규
    • Journal of Chest Surgery
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    • 제16권3호
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    • pp.310-315
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    • 1983
  • The combined anomaly of pulmonary stenosis with atrial or ventricular septal defects is usually associated with decreased pulmonary blood flow and right to left shunt, and result in generalized cyanosis. Non-cyanotic pulmonary stenosis patients have generally been considered to have isolated pulmonary stenosis with intact septa. We are going to report a case of pulmonary stenosis with septal defects who have no frank cyanosis at rest because of the predominant intracardiac shunt from left to right. Recently, we managed surgically a case of pulmonary valvular stenosis combined with secundum type atrial septal defect, type II ventricular septal defect, and patent ductus arteriosus. The clinical manifestations of this patient were exertional dyspnea, frequent upper respiratory infection, chest discomfortness and lethargy since late childhood and these had been progressively aggravated. Pulmonary valvular stenosis, atrial septal defect and ventricular septal defect were closed through simply right atriotomy and patent ductus arteriosus through pulmonary arteriotomy. Immediate postoperative course was uneventful and one year follow up is excellent.

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Persistent Atrial Fibrillation Related to a Congenital Pericardial Defect and Left Atrial Appendage Herniation

  • Lee, Heemoon;Jeong, Dong Seop;Kim, In Sook;Park, Byung Jo
    • Journal of Chest Surgery
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    • 제48권6호
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    • pp.429-431
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    • 2015
  • Congenital pericardial defects (CPDs) are infrequent anomalies that are usually asymptomatic and are discovered incidentally during unrelated interventions. Here we report the case of a CPD with herniation of an enlarged left atrial appendage identified during total thoracoscopic ablation (TTA) for persistent atrial fibrillation (AF). The persistent AF was successfully treated with a hybrid procedure, in which TTA was followed by an electrophysiological study.

Sternal Resection and Reconstruction for Solitary Plasmacytoma of the Sternum: Case Report

  • Choi, Chang Woo;Park, You Kyeong;Shin, Hwa Kyun;Lim, Jae Woong;Her, Keun
    • Journal of Chest Surgery
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    • 제54권5호
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    • pp.400-403
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    • 2021
  • A 63-year-old patient was admitted with a sternal fracture and mass. On evaluation, most of the body of the sternum had been destroyed by a tumor. Radical resection of the sternum was performed and part of the major pectoral muscles adherent to the sternal tumor was also resected. The chest wall defect was reconstructed with mesh, bone cement, and a titanium rib plate system. Reconstruction with this method seemed to be an appropriate procedure to prevent instability of the chest wall.

심실 중격 결손과 대동맥 판 협착을 가진 대동맥 궁 단절의 일차 완전 교정술 -1예 보고- (One-stage Repair of Interrupted Aortic Arch with Ventricular Septal Defect and Valvular Aortic Stenosis - A case report-)

  • 조준용;정영균;이종태;김규태;장봉현
    • Journal of Chest Surgery
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    • 제38권12호
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    • pp.856-859
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    • 2005
  • 생후 19일 된 남아가 안면 청색증과 과호흡을 주소로 내원하였다. 심 초음파 소견 상 B형의 대동맥 궁 단절과 후방 부정열형의 심실 중격 결손, 대동맥 판 협착을 보였다. 수술은 양심실 교정을 시행하였으며, 대동맥 판과 폐동맥 판 모두를 좌심실 유출로로 이용하고 신 대동맥 궁을 재건하고 Goretex graft를 이용하여 우심실 유출로를 재건하는 새로운 방법으로 하였다. 술 후 좌심실 유출로와 우심실 유출로 모두 협착없이 잘 유지되었다.

Efficacy of the Maze Procedure for Atrial Fibrillation Associated with Atrial Septal Defect

  • Shim, Hunbo;Yang, Ji-Hyuk;Park, Pyo-Won;Jeong, Dong Seop;Jun, Tae-Gook
    • Journal of Chest Surgery
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    • 제46권2호
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    • pp.98-103
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    • 2013
  • Background: Atrial fibrillation (AF) is a common complication in elderly patients with atrial septal defect (ASD). The purpose of this study was to examine the efficacy of the maze procedure in these patients. Materials and Methods: Between February 2000 and May 2011, 46 patients underwent the maze procedure as a concomitant operation with ASD closure. Three patients who underwent a right-sided maze were excluded, and one patient was lost to follow-up. The mean follow-up duration was $3.2{\pm}2.5$ years. Electrocardiography was performed 1 month, 3 months, 6 months, and 1 year after surgery, and checked annually after that. Results: AF persisted in 4 patients after surgery. One year after surgery, among 38 patients, 55.3% remained in sinus rhythm without antiarrhythmic drugs. However, when including the patients who took antiarrhythmic drugs, 92.1% were in sinus rhythm. Freedom from AF recurrence at 3 months, 6 months, 1 year, 2 years, 3 years, and 5 years after surgery were $97.4{\pm}2.6$, $94.4{\pm}3.8$, $91.2{\pm}4.9$, $87.8{\pm}5.8$, $79.5{\pm}7.6$, and $68.2{\pm}12.4$, respectively. There was no early mortality after operation. Conclusion: Concomitant treatment with the maze procedure and ASD closure is safe and effective for restoring the sinus rhythm.

반회전 동맥간 전환술 후 양심실 유출로의 중단기 변화 - 2예 보고 - (Changes of the Biventricular Outflow Tract after a Half Turned Truncal Switch Operation in Patients with Transposition of the Great Arteries, a Ventricular Septal Defect and Pulmonary Stenosis - 2 case reports -)

  • 김정원;조준용;김근직;이종태;김규태
    • Journal of Chest Surgery
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    • 제43권1호
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    • pp.58-62
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    • 2010
  • 심실 중격 결손과 폐동맥 협착을 가지고 있는 대혈관 전위 환자의 수술적 치료방법으로 Rastelli 수술법이 보편화되어 왔으나, 추적 관찰 중에 심장외 도관의 폐쇄, 좌심실 유출로의 폐쇄, 부정맥이 높은 확률로 발생하는 등의 장기 성적이 만족스럽지 못하였다. 이와 같은 문제점을 해결하기 위해 본원에서 2003년과 2006년에 심실 중격 결손과 폐동맥 협착을 가지고 있는 대혈관 전위 환자 2명을 반회전 동맥간 회전술 및 Lecompte 술식을 이용하여 수술하였고, 추적 관찰을 통해 양심실 유출로의 중기 변화에 대한 경험을 보고한다.

잔여 하정맥동형 심방중격결손증의 재수술 (Reoperation for the Missed Inferior Sinus Venous Atrial Septal Defect)

  • 유병수;조태준;김건일;이재웅;홍기우;이원용
    • Journal of Chest Surgery
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    • 제39권2호
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    • pp.154-156
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    • 2006
  • 난원와 하부에 위치하는 하정 맥동형 심방중격결손증(inferior sinus venclsus defect)은 매우 드문 선천성심질환으로 수술 전 이차공형 심방중격결손증과 감별이 어렵고 수술 중에도 발견하기가 쉽지 않다. 저자들은 10세 때에 심방중격결손증으로 단순 봉합술 시행 후 별 문제없이 지내다가 이비인후과 수술 위한 사전 검사로 시행한 심장초음파 검사상 잔여 심방중격결손증이 발견된 24세 여자 환자에서 심방중격결손증 재수술을 시행하였다. 환자는 이차공형 심방중격결손증과 하정맥동형 심방중격결손증을 동시에 가지고 있었으나 일차수술에서 하정맥동형 심방중격결손증을 발견하지 못하여 이차공형 심방중격결손증만 교정된 상태였고, 금번 재수술에서 하정맥동형 심방중격결손증을 확인하고 패취 봉합을 시행하였다.

선천성심질환(先天性心疾患)의 심폐기(心肺器) 개심수술(開心手術) - 4례(例) 보고(報告) - (Open Heart Surgery of Congenital Heart Diseases -Report of Four Cases-)

  • 김근호;박영관;지행옥;김영태;이종배;정윤채;오철수
    • Journal of Chest Surgery
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    • 제9권1호
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    • pp.1-9
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    • 1976
  • The present. study reports four cases of congenital heart diseases, who received open heart surgery by the Sarn's Heart-Lung-Machine in the department of Thoracic Surgery, Hanyang University Hospital during the period between July 1975 and May 1976. The Heart-Lung-Machine consisted of the Sarn's five head roller pump motor system (model 5000), heat exchanger, bubble trap, the Rygg-Kyvsgaard oxygenator, and monitors. The priming of pump oxygenator was carried out by the hemodilution method using Hartman's solution and whole blood. Of the four cases of the heart diseases, three whose body weight were below 30kg, received the partial hemodilution priming and the remaining one whose body weight was 52kg received the total hemodilution priming with Hartman's solution alone. The rate of hemodilution was in the average of 60.5ml/kg. Extracorporeal circulation was performed at the perfusion flow rate of the average 94.0ml/kg/min, and at the moderate hypothermia between 35'5"C and 30'5"C of the rectal temperature. In the total cardiopulmonary bypass, arterial blood pressure was anged between 30 mmHg and 85 mmHg, generally maintaining over 60 mmHg and venous pressure was measured between 4 and $23cmH_2O$, generally maintaining below $10cmH_2O$. The first case: The patient, a nine year old girl having the symptoms and physical signs typical to cardiac anomaly was definitely diagnosed as isolated pulmonary stenosis through the cardiac catheterization. There was, however, no cyanosis, no pathological finding by X-ray and E.C.G. tracings. The valvulotomy was performed through the arteriotomy of pulmouary artery under the total cardiopulmonary bypass. Postoperative course of the patient was uneventful, and murmur and the clinical symptoms disappeared. The second case: A 12 year old boy with congenital heart anomaly was positively identified as having ventricular septal defect through the cardiac catheterization. As in the case with the first case, the patient exhibited the symptoms and physical signs typical to cardiac anomaly, but no pathological abnormality by X-ray and E.C.G. tracings. The septal defect was localized on atrioventricular canal and was 2 by 10 mm in size. The septal defect was closed by direct simple sutures under the cardiopulmonary bypass. Postoperative hemodynamic study revealed that the pressure of the right ventricle and pulmonary artery were decreased satisfactory. Postoperative course of the patient was uneventful, and murmur and the clinical symptoms disappeared. The third case: The patient, a 19 year old girl had been experienced the clinical symptoms typical to cardiac anomaly for 16 years. The pink tetralogy of Fallot was definitey diagnosed through the cardiac catheterization. The patient was placed on an ablolute bed rest prior to the operation because of severe exertional dyspnea, fatigability, and frequent syncopal attacks. However, she exhibited very slight cyanosis. Positive findings were noted on E.C.G. tracings and blood picture, but no evidence of pathological abnormality on X-ray was observed. All of the four surgical approaches such as Teflon patch closure (3 by 4cm in size) of ventricular septal defect, myocardial resection of right ventricular outflow tract, valvulotomy of pulmonary valvular stenosis, and pericardial patch closing of ventriculotomy wound were performed in 95 minutes under the cardiopulmonary bypass. Postoperative hemodynamic study revealed that the pressure of the right ventricle was decreased and pulmonary artery was increased satisfactorily. Postoperative course of the patient was uneventful, and murmur and the clinical symptoms disappeared. The fourth case: The patient, a 7 1/4 year old girl had the symptoms of cardiac anomaly for only three years prior to the operation. She was positively identified as having acyanotic tetralogy of Fallot by open heart surgery. The patient showed positive findings by X-ray and E.C.G. tracings, but exhibited no cyanosis and normal blood picture. All of the three surgical approaches, such a myocardial resection of hypertrophic sight ventricular outflow tract, direct suture closing of ventricular septal defect and pericardial patch closing of ventriculotomy wound were carried out in 110 minutes under the cardiopulmonary bypass. Postoperative hemodynamic study revealed that the pressure of the right ventricle was decreased and pulmonary artery was increased satisfactorily. Postoperative course of the patient was uneventful, and the symptoms disappeared.

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Partial Atrioventricular Canal Defect in a Maltese Dog

  • Lee, Seung-Gon;Nam, So-Jeong;Moon, Hyeong-Sun;Hyun, Chang-Baig
    • 한국임상수의학회지
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    • 제25권3호
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    • pp.195-199
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    • 2008
  • A 2-year-old female Maltese dog was referred with primary complaints of exercise intolerance and abnormal heart sound. Clinical and diagnostic investigation revealed split S2 and S4 gallop in the cardiac auscultation, tall P wave and left anterior fascicular block in the electrocardiogram, left atrial enlargement on the thoracic radiography, ostium primum atrial septal defect and cleft of the anterior leaflet of the mitral valve on the echocardiography. Based on those findings, the dog was diagnosed as the partial atrioventricular canal defect. Since the dog showed mild exercise intolerance, enalapril and furosemide were prescribed.