• Clinical and Experimental Pediatrics
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• 제46권8호
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• pp.826-830
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• 2003

본 저자들은 출생 후 늘어지며 경구 수유를 잘 하지 못하는 증상으로 본원에서 ARCI 증후군 진단을 받고 경구용 bicarbonate, 1,25-dihydroxycholecalciferol, 비 경구 수유와 폐렴 치료를 받았으나 사망한 1례를 경험하여 이를 보고하는 바이다. 다발성 관절 구축, 신세뇨관성 산증, 담즙 정체성 간염은 ARCI 증후군의 기본적인 임상 증상이기는 하나 이들이 모두 혹은 동시에 나타나는 것은 아니므로 신생아 시기에 늘어지며 관절구축을 보이고 산증이 있는 경우 주의 깊은 추적 관찰을 통해 진단을 내리도록 해야할 것이다. 또한 이들은 성장 부진과 잦은 감염에 시달리게 되므로 일찍부터 비관 삽입 등을 통한 영양이나 감염의 증후를 잘 관찰함으로써 적절한 성장을 할 수 있도록 도와야겠다.

• Journal of Chest Surgery
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• 제31권2호
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• pp.168-172
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• 1998

하정맥동 결손(inferior sinus venosus defect)은 하대정맥과 우심방의 경계 부위에 발생하는 심방중격결손의 한 형태로 매우 드문 선천성 심장질환이며, 심방중격의 하부 뒤쪽에 위치하고 한 개 이상의 우 폐정맥의 환류 이상을 동반하고 있어 개심술시 정확한 교정을 요하므로 수술 전 또는 수술 중 정확한 해부학적 진단이 선행되어야 한다. 저자들은 부분 폐정맥 환류이상을 동반한 하정맥동형 심방중격결손 4예를 치험하였다. 1예는 25세 성인이었고 3예는 14개월 미만의 영아 및 소아였다. 4예 모두 심부전 때문에 수술했으며 이중 4개월의 영아는 긴급 수술이 필요했다. 진단을 위해 심초음파 및 도플러 검사와 심도자법을 시행하였다. 수술전 확진은 1예에서 가능했고 3예는 수술전 병변을 의심하고 수술시 확진되었다. 수술방법으로 이상 환류되는 폐정맥이 좌심방으로 환류 되도록 자가심막을 이용하여 심방중격결손을 폐쇄하였다. 4예 모두 수술 결과는 양호하였으며 초음파 검사의 추적에서 하대정맥과 폐정맥의 환류장애 소견은 없었다. 정확한 수술 교정을 위해 수술전 정확한 진단이 필수적이며, 수술전 폐정맥의 부분 환류이상과 심방중격 결손으로 진단된 환자에서는 수술중 하정맥동 결손의 여부를 확인하여 적절한 수술적 교정을 시행해야 할 것으로 사료된다.

• Clinical and Experimental Pediatrics
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• 제52권4호
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• pp.494-498
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• 2009

목 적 : 심방중격결손의 기구 폐쇄술은 현재 소아 영역에서 수술을 대체할 치료법으로 광범위하게 사용되고 있으나 수술과 비교하였을 때 적절한 시행 시기는 명확하지 않다. 본 연구에서는 3세 미만의 심방중격결손 소아에서 기구 폐쇄술의 안전성, 효용성 및 임상 결과를 평가하여 시술을 시행하기에 적절한 시기를 알아보고자 하였다. 방 법 : 2003년 5월부터 2005년 12월까지 연세대학교 의과대학 심장혈관병원 소아심장과에서 Amplatzer septal occluder(ASO)를 이용한 심방중격결손의 기구 폐쇄술을 시행 받은 환자 295명 중 3세 미만 소아 51명을 대상으로 하였다. 시술 소요 시간, 투시 검사 시간, 폐쇄 성공률, 잔류 단락율, 합병증의 종류 및 발생 빈도를 조사하였고, 기구 장착 전후의 체폐순환비, 폐동맥압, 우심실압을 측정하였으며 시술 후 1일, 1개월, 6개월, 12개월 및 이후 1년 간격으로 경흉부 심초음파를 시행하여 추적 관찰하였다. 결 과 : 대상 환자의 75% (38/51)가 여자였으며, 시술 당시 연령은 $2.0{\pm}0.6$세, 체중은 $11.8{\pm}1.7$ kg, 심방 중격 결손의 크기는 $16.6{\pm}3.6$ mm, 이들의 체폐순환비는 $2.4{\pm}0.9$이었고, 기구 폐쇄술 시행 후 추적 관찰 기간은 $19.8{\pm}6.4$개월이었다. 시술의 폐쇄성공률은 98% (50/51), 소요 시간은 $87.7{\pm}23.6$분, 방사선 투시 시간은 $31.8{\pm}14.7$분이었으며 잔류 단락은 시술 후 24시간 뒤 51명중 7명(15%)에서 관찰되었으나, 최종 추적 관찰 시에는 모두 폐쇄되었다. 폐쇄술 시행 전과 시행 직후의 체폐순환비는 $2.4{\pm}0.9$에서 $1.4{\pm}0.3$ (P<0.001)으로, 주폐동맥압은 $28.4{\pm}6.4$ mmHg에서 $25.5{\pm}5.6$ mmHg (P=0.04)로, 우심실압은 $41.3{\pm}11.8$ mmHg에서 $32.6{\pm}7.9$ mmHg (P<0.001)로 감소하였다. 대상 환자 중 2명에서 시술과 관련한 합병증이 있었으며 기구 이탈과 관련한 우심방 색전증 1예, 서혜부에 발생한 혈종 1예가 관찰되었다. 결 론 : 심방중격결손 소아에서 ASO를 이용한 경피적 심방중격결손 폐쇄술은 3세 미만의 작은 소아에서 안전하고 효과적으로 시행할 수 있으며 더 성장하기까지 시술을 연기할 필요는 없는 것으로 생각된다. 작은 영아에서의 효용성과 안전성에 대해서는 더 광범위한 연구가 필요하다.

• Journal of Chest Surgery
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• 제14권1호
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• pp.49-59
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• 1981

This is one case report of surgically treated partial atrioventricular canal. The 22 year-old male patient had no definitive history of frequent respiratory infection and cyanosis in his early childhood. Since his age of 7 years, dyspnea was manifested on exertion. First appearance of congestive heart failure was at his age of 16 years old. The physical examination revealed that the neck veins were distended and heaving of precordium. A thrill was palpable on the left 3rd-4th intercostal space extending from the sternal border toward the apex and Grade IV/VI systolic ejection murmur was audible on it. Neither cyanosis nor clubbing was noted. Liver was palpable about 5 finger breadths. Chest X-ray revealed increased pulmonary vascularity and severe cardiomegaly (C-T ratio = 74%). EKG revealed LAD, clockwise rotation, LVH and trifascicular block. Echocardiogram showed paradoxical ventricular septal movement, narrowed left ventricular outflow tract and abnormal diastolic movement of the anterior leaflet of mitral valve. Right heart catheterization resulted in large left to right shunt (Qp : Qs = 5.7: 1), ASD and moderate pulfllonary hypertension. Finally, left ventriculogram revealed typical goose neck appearance of left ventrlcalar outflow tract. On Oct. 10, 1980, open heart surgery was performed. Operative findings were: 1. Large primum defect ($6{\times}5$ Cm in diameter) 2. Cleft on the anterior leaflet of mitral valve. 3. The upper portion of ventricular septum was descent but no interventricular communication. 4. Downward attachment of the atrioventricular valves on the ventricular muscular septum. 5. Medium sized secumdum defect ($2{\times}1$ Cm in diameter). The cleft was repaired with 4 interrupted sutures. The primum defect was closed with Teflon patch and the secundum defect was closed with direct suture closure. Postoperatively atrial flutter-fibrillation in EKG and Grade U/VI apical systolic murmur were found. The postoperative course was uneventful and discharged on 29th postoperative day in good general conditions.

• Journal of Chest Surgery
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• 제23권3호
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• pp.474-481
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• 1990

We have experienced 44 cases of coarctation of aorta in the age of infancy and children from April 1986 to September 1989 at Seoul National University Children`s hospital. Patients were thirty males and fourteen females, and their age ranged from one month to ten years[mean 23.84 $\pm$33.06 months] with thirty-two infant cases. In the infantile age, congestive heart failure was the most common chief complaint[18/32], and above that age, frequent upper respiratory infection was most common[8/12]. We experienced thirteen cases of isolated COA, twenty-two cases of COA with VSD, eight cases of COA with VSD, eight cases of COA with intracardiac complex anomalies and one case of COA with atrial septal defect. The associated intracardiac complex anomalies were three Taussig-Bing type double outlet right ventricle, one single ventricle, one transposition of great arteries, one atrioventricular septal defect, one hypoplastic aortic arch with left heart hypoplasia, and one Tetralogy of Fallot. Operative techniques of COA were twenty-three subclavian flap arterioplasty, 12 resection and end to end anastomosis, eight onlay patch angioplasty, and I direct angioplasty after resection of web. Among the cases with other cardiac anomalies, staged operation was done in twenty-nine patients, and single stage total correction was performed only in three patients. There were seven operative mortality[15.9%], all being in infantile age group, and among fourteen cases associated with large VSD[Qp/Qs>2.0, mean pulmonary arterial pressure>50mmHg], four patients were died, but there was no mortality in patients with small VSD. With above results, we are intended to discuss about the interval between staged operation, the fate of VSD after coarctoplasty in case of COA with VSD, causes of death, complications etc.

• Clinical and Experimental Pediatrics
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• 제49권8호
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• pp.895-897
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• 2006

폐 격리증이 없는 정상적인 폐에 체 혈관이 이상 기시하는 것은 매우 드문 질환이다. 저자들은 반복적인 하기도 감염을 보이는 영아에서 선천성 심장질환의 상태가 본 하기도 감염을 나타낼 정도로 심하지 않음을 이상히 여겨 컴퓨터 단층 촬영을 시행하였다. 그 결과 폐 격리증이 없는 폐의 이상 체 동맥 기시가 우측 폐하 엽에 존재함과 동시에 우측 하엽 폐동맥이 없는 사실을 확인하게 되었다. 어린 나이에 이 같은 선천성 질환의 조합은 이전에 보고 된 바가 없는 매우 드문 질환으로 생각된다.

• Journal of Chest Surgery
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• 제19권1호
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• pp.116-121
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• 1986

Patients over 15 years of age who have undergone a surgical correction of a congenital cardiac malformation during period of January 1958 through January 1986 have been reviewed. During this period there were 3957 congenital cardiac lesions consisting of 2712 acyanotic and 1245 cyanotic cases. Among them, a total of 725 adults [18.3%] with a variety of congenital heart lesions, 548 acyanotic group and 177 cyanotic group were operated on. 372 patients were male and 252 patients were female. There were 280 patients under 20 years of age, 206 between 20-24 years, 102 between 25-29 years, 48 between 30-34 and 89 over 35 years. The most common defects were atrial septal defect which accounted for 207 cases [28.6%] and other common anomalies were VSD [140 cases, 19.3%], TOF [136 cases, 18.6%], PDA [120 cases, 16.6%] and PS [33 cases, 4.6%] in order of incidence. Overall operative mortality for this series was 3.6% [1.8% of a cyanotic group and 9.0% of cyanotic group] compared with 2.8% of total cases of congenital heart disease [acyanotic group 1.1% and cyanotic group 6.5%]. This reviewed series reveals the incidence of operable congenital heart defects appearing in any adult life and demonstrates that surgical repair can be accomplished with a satisfactory low mortality rate.

• Journal of Chest Surgery
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• 제12권3호
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• pp.281-288
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• 1979

For years, physicians and anatomists have been interested in the heart that has one functioning ventricle. Various terms have been suggested for this entity including single ventricle, common ventricle, double-inlet left ventricle, cor biatriatum triloculare, and primitive ventricle. In this report, the term "single ventricle" is utilized as suggested by Van Praagh, and is defined as that congenital cardiac anomaly in which a common or separate atrioventricular valves open into a ventricular chamber from which both great arterial trunks emerge. An outlet chamber, or infundibulum, may or may not be present and give rise to the origin of either of the great arteries. This definition excludes the entity of mitral and tricuspid atresia. An 11 year old cyanotic boy was admitted chief complaints of exertional dyspnea and frequent upper respiratory infection since 2 weeks after birth. He was diagnosed as inoperable cyanotic congenital heart disease, and remained without any corrective treatment up to his age of 11 year when he suffered from aggravation of symptoms and signs of congestive heart failure for 2 months before this admission. On 22nd of May 1979, he was admitted for total corrective operation under the impression of tricuspid atresia suggested by a pediatrician. Physical check revealed deep cyanosis with finger and toe clubbing, and grade V systolic ejection murmur with single second heart sound was audible at the left 3rd intercostal space. Development was moderate in height [135 cm] and weight[28Kg]. Routine lab findings were normal except increased hemoglobin [21.1gm%], hematocrit [64 %], and left axis deviation with left ventricular hypertrophy on EKG. Cardiac catheterization and angiography revealed 1-transposition of aorta, pulmonic valvular stenosis, double inlet of a single ventricle with d-loop, and normal atriovisceral relationship [Type III C solitus according to the classification of Van Praagh]. At operation, longitudinal incision at the outflow tract of right ventricle in between the right coronary artery and its branch [LAD from RCA] revealed high far anterior aortic valve which had fibrous continuity with mitral annulus, and pulmonic valve was stenotic up to 4 mm in diameter positioned posterolaterally to the aorta. Ventricular septum was totally defective, and one markedly hypertrophied moderator band originated from crista supraventricularis was connected down to the imaginary septum of the ventricular cavity as a pseudoseptum of the ventricle. Size of the defect was 3X3 cm2 in total. Patch closure of the defect with a Teflon felt of 3.5 x 4 cm2 was done with interrupted multiple sutures after cut off of the moderator band, which was resutured to the artificial septum after reconstruction of the ventricular septum. Pulmonic valvotomy was done from 4 mm to 11 mm in diameter thru another pulmonary arteriotomy incision, and right ventriculotomy wound was closed reconstructing the right ventricular outflow tract with pericardial autograft of 3 x 4 cm2. Atrial septal defect of 2 cm in diameter was closed with 3-0 Erdeck suture, and atrial wall was sutured also when rectal temperature reached from 24`C to 35.5`C. Complete A-V block was managed with temporary external pacemaker with a pacing rate of 110/min. thru myocardial wire, and arterial blood pressure of 80/50 mmHg was maintained with Isuprel or Dopamine dripping under the CVP of 25-cm saline. Consciousness was recovered one hour after the operation when his blood pressure reached 100 /70 mmHg, but vital signs were not stable, and bleeding from the pericardial drainage and complete anuria were persisted until his heart could not capture the pacemaker impulse, and patient died of low output syndrome 320 min after the operation.

• Journal of Chest Surgery
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• 제12권3호
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• pp.289-296
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• 1979

For years, physicians and anatomists have been interested in the heart that has one functioning ventricle. Various terms have been suggested for this entity including single ventricle, common ventricle, double-inlet left ventricle, cor biatriatum triloculare, and primitive ventricle. In this report, the term "single ventricle" is utilized as suggested by Van Praagh, and is defined as that congenital cardiac anomaly in which a common or separate atrioventricular valves open into a ventricular chamber from which both great arterial trunks emerge. An outlet chamber, or infundibulum, may or may not be present and give rise to the origin of either of the great arteries. This definition excludes the entity of mitral and tricuspid atresia. An 11 year old cyanotic boy was admitted chief complaints of exertional dyspnea and frequent upper respiratory infection since 2 weeks after birth. He was diagnosed as inoperable cyanotic congenital heart disease, and remained without any corrective treatment up to his age of 11 year when he suffered from aggravation of symptoms and signs of congestive heart failure for 2 months before this admission. On 22nd of May 1979, he was admitted for total corrective operation under the impression of tricuspid atresia suggested by a pediatrician. Physical check revealed deep cyanosis with finger and toe clubbing, and grade V systolic ejection murmur with single second heart sound was audible at the left 3rd intercostal space. Development was moderate in height [135 cm] and weight[28Kg]. Routine lab findings were normal except increased hemoglobin [21.1gm%], hematocrit [64 %], and left axis deviation with left ventricular hypertrophy on EKG. Cardiac catheterization and angiography revealed 1-transposition of aorta, pulmonic valvular stenosis, double inlet of a single ventricle with d-loop, and normal atriovisceral relationship [Type III C solitus according to the classification of Van Praagh]. At operation, longitudinal incision at the outflow tract of right ventricle in between the right coronary artery and its branch [LAD from RCA] revealed high far anterior aortic valve which had fibrous continuity with mitral annulus, and pulmonic valve was stenotic up to 4 mm in diameter positioned posterolaterally to the aorta. Ventricular septum was totally defective, and one markedly hypertrophied moderator band originated from crista supraventricularis was connected down to the imaginary septum of the ventricular cavity as a pseudoseptum of the ventricle. Size of the defect was 3X3 cm2 in total. Patch closure of the defect with a Teflon felt of 3.5 x 4 cm2 was done with interrupted multiple sutures after cut off of the moderator band, which was resutured to the artificial septum after reconstruction of the ventricular septum. Pulmonic valvotomy was done from 4 mm to 11 mm in diameter thru another pulmonary arteriotomy incision, and right ventriculotomy wound was closed reconstructing the right ventricular outflow tract with pericardial autograft of 3 x 4 cm2. Atrial septal defect of 2 cm in diameter was closed with 3-0 Erdeck suture, and atrial wall was sutured also when rectal temperature reached from 24`C to 35.5`C. Complete A-V block was managed with temporary external pacemaker with a pacing rate of 110/min. thru myocardial wire, and arterial blood pressure of 80/50 mmHg was maintained with Isuprel or Dopamine dripping under the CVP of 25-cm saline. Consciousness was recovered one hour after the operation when his blood pressure reached 100 /70 mmHg, but vital signs were not stable, and bleeding from the pericardial drainage and complete anuria were persisted until his heart could not capture the pacemaker impulse, and patient died of low output syndrome 320 min after the operation.

• Journal of Chest Surgery
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• 제36권9호
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• pp.683-686
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• 2003

우심실 형성부전이 있으면서 단신방, 그리고 스펀지 좌심실이 있는 매우 드문 질환인 독립된 우심실 형성부전 환아를 경험하였다. 수술 전 우심실의 크기는 좌심실의 반이었으며 삼첨판막의 크기는 z-value로 -4이었다. 수술 시 6세였으며 수술은 양심실성 교정을 시도하여 심방을 2개로 나누어주었으며 3mm 구멍을 남겨 두었다. 수술 후 경과는 좋았으며 외래 추적에서 우심실 기능 부전소견은 없었다. 술 후 27개월에 심도자가 시행되었으며 삼참판막은 잘 자랐으며(z-value=-0.4), 심방중격의 구멍은 저절로 막혔음을 확인하였다. 독립된 우심실 형성부전을 경험하여 성공적으로 양심실성 교정을 시행하였기에 보고하는 바이다.