- Original Article
- Mid-term Result of the Transcatheter Occlusion of Patent Ductus Arteriosus with Duct-Occlud Device and Procedure-Related Problems
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Yuria Kim, Jae Young Choi, Jong Kyun Lee, Jun Hee Sul, Sung Kyu Lee, Young Hwan Park, Bum Koo Cho
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Clin Exp Pediatr. 2004;47(1):36-43. Published online January 15, 2004
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Purpose : We will present our mid-term result of transcatheter closure of PDA with Duct-Occlud device(pfm. AG. Germany) after 12 months follow up and report the problems during the procedure.
Methods : In total 154 patients, the Duct-Occlud devices were inserted in our institute from March, 1996 to August, 2002. Three types of Duct-Occlud device, i.e standard, reinforced, reinforced reverse cone... |
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- The Natural Course and Size Change of Atrial Septal Defect Secundum
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Deok Young Choi, Jae Young Choi, Mi Jin Kim, Jun Hee Sul, Sung Kyu Lee
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Clin Exp Pediatr. 2003;46(9):871-875. Published online September 15, 2003
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Purpose : This study was performed to follow the natural course and size change of isolated atrial septal defect(ASD) secundum.
Methods : Among the newly diagnosed with ASD secundum at the division of pediatric cardiology in Yonsei cardiovascular hospital from January 1996 to December 2000, 89 patients with pure ASD secundum were checked by the serial echocardiographic evaluation to measure... |
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- Medico-Surgical Cooperative Treatment of Pulmonary Atresia with Intact Ventricular Septum
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Kyeong Sik Kim, Byeong Chul Kweon, Jong Kyun Lee, Jae Young Choi, Jun Hee Sul, Sung Kyu Lee, Young Whan Park, Bum Koo Cho
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Clin Exp Pediatr. 2003;46(3):250-258. Published online March 15, 2003
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Purpose : The actual clinical examples of co-appliance of catheter intervention with surgical procedures in the treatment of pulmonary atresia with an intact ventricular septum(PA/IVS) which we have experienced in our institution are here shown, and the anatomical and hemodynamical profiles between each method is compared.
Methods : Medical records of 33 patients with PA/IVS who underwent various treatment from January,... |
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- Postoperative Progress and Influencing Factors in Patients after Rastelli Procedure
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Se Heui Kim, Kyeong Sik Kim, Jong Kyun Lee, Jae Young Choi, Jun Hee Sul, Sung Kyu Lee, Young Whan Park, Bum Koo Cho
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Clin Exp Pediatr. 2003;46(3):259-264. Published online March 15, 2003
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Purpose : We have performed an analysis on patients who received Rastelli operation in our institute and reviewed their progress postoperatively. Various factors with suspected relationship to the outcome have been considered to help in future treatment and follow-up.
Methods : We analyzed retrospectively 43 patients who either received Rastelli operation in Yonsei University Cardiovascular Center from March 1995 to April... |
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- Conversion of Total Atrio-pulmonary Connection to
Total Cavo-pulmonary Connection
- Review of Indications and Hemodynamic Characteristics -
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Jung Ho Seo, Jong Kyun Lee, Jae Young Choi, Jun Hee Sul, Sung Kyu Lee, Young Whan Park, Bum Koo Cho
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Clin Exp Pediatr. 2002;45(2):199-207. Published online February 15, 2002
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Purpose : Since the successful application of total atrio-pulmonary connection(TAPC) to patients with various types of physiologic single ventricles in 1971, post-operative survival rates have reached more than 90%. However some patients have been shown to present with late complications such as right atrial thrombosis, atrial fibrillation and protein losing enteropathy eventually leading to re-operation to control the long-term complications.... |
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- Results of Balloon Angioplasty in Patients with Coarctation of the Aorta
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Hyun Kyung Roh, Bong Hee Seo, Jae Young Choi, Jin Sung Ko, Jong Kyun Lee, Jun Hee Sul, Sung Kyu Lee
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Clin Exp Pediatr. 2001;44(12):1404-1412. Published online December 15, 2001
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Purpose : This study was undertaken to analyze and compare the effects of percutaneous balloon
angioplasty(BAP) on postoperative re-coarctation and native coarctation of the aorta(CoA) and to
thereby contribute to the development of treatment methods for CoA.
Methods : The subjects in this study were 21 children who had undergone BAP from Jan. 1996
to Dec. 2000 in the Division of Yonsei Pediatric Cardiology.... |
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- Early Results of Stent Implantation in Branch Pulmonary Artery Stenosis after Tetralogy of Fallot Repair
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Sung Kyu Lee, Sang Hun Lee, Jae Young Lee, Su Jin Kim, Mi Young Han, Do Jun Cho, In Seung Park, Eun Jung Bae, Sung Ho Kim
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Clin Exp Pediatr. 2000;43(10):1343-1349. Published online October 15, 2000
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Purpose : Pulmonary artery stenosis is mainly complicated by aortopulmonary shunt or total correction of tetralogy of Fallot(TOF). Results of surgical angioplasty are poor and the success rate of balloon angioplasty is 53-72%. Endovascular stents have been applied to these lesions. The purpose of this study is to evaluate the early results of stent implantation in postoperative pulmonary artery stenosis... |
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- The Use of Quadruple Blood Bags Transfusion of Low Birth Weight Neonates
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Sang Hoon Lee, Jean Yoon, Yang Park, Sung Kyu Lee, Hee Chung Kim, Woo Sup Shim
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Clin Exp Pediatr. 1999;42(8):1122-1129. Published online August 15, 1999
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Purpose : Low-birth-weight(LBW) neonates often need multiple transfusions during their neonatal period. The routine use of the 500ml mono-bag system in Korea, even in neonatal transfusions, results in a great waste of blood and exposes the neonate to multiple blood donors. To reduce the waste of blood and the number of exposures, we used quadruple blood bags in the transfusion... |
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- Case Report
- A Case of Kawasaki Disease of Five Recurrences During 4 Years
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Jeong Woo Ryu, Dong Soo Kim, Jong Kyun Lee, Jun Hee Sul, Sung Kyu Lee
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Clin Exp Pediatr. 1997;40(9):1293-1296. Published online September 15, 1997
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Kawasaki disease is an acute illness of early childhood, especially less than 5 years of age,
characterized by prolonged fever(> 5 days), changes of lips and oral cavity, changes of peripheral
extremities, polymorphous skin rash, bilateral conjunctival congestion and acute nonpurulent cervical
lymphadenopathy. Usually, the recurrence of Kawasaki disease is not frequent.
It is thought that the factors in recurrence of Kawasaki disease was... |
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- Unilateral Absence of Pulmonary Artery
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Gu Hyun Lee, Jae Young Choi, Jong Kyun Lee, Jun Hee Sul, Sung Kyu Lee
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Clin Exp Pediatr. 1996;39(9):1309-1314. Published online September 15, 1996
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Unilateral absence of pulmonary artery(UAPA) is a rare disease. We experienced 2 cases of
UAPA in 5 month-old male patient and 16 year-old female patient with the chief complaint of
dyspnea. Lung perfusion scan, cardiac catheterization with pulmonary and aortic angiography
confirmed the diagnosis of UAPA. |
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- Original Article
- Hemodynamic Status of Subpulmonic Ventricular Septal Defect in Relation to Morphologic Changes of Aortic Valve
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Myung Hyun Sohn, Jae Young Choi, Jong Kyun Lee, Jun Hee Sul, Sung Kyu Lee, Bum Koo Cho
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Clin Exp Pediatr. 1996;39(8):1103-1110. Published online August 15, 1996
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Purpose : Subpulmonic ventricular septal defect is clinically important because the risks of
aortic regurgitation and endocarditis are substantially increased. This study was conducted to
evaluate the effect of hemodynamic changes induced by structural anomalies of aortic valve on
the surgical outcome.
Methods : This clinical study was done by reviewing the medical records of 124 patients who
were diagnosed and surgically managed at the... |
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- Erratum
- Transcatheter Closure of Secundum Atrial Septal Defect with \Buttoned\" Device"
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Jong-Kyun Lee, Seok Min Choi, Jo Won Jung, Jun Hee Sul, Sung Kyu Lee, Jin Yong Lee, Hae Yong Lee
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Accepted January 1, 1970
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Purpose : Recently, non-operative transcatheter management of congenital heart defects h as increased due to their effectiveness and safety being acknowledged. In the case of secundu- m atrial septal defect(ASD), closing devices have been developed since 1974 and have been u sed clinically. The authors, having tried the "Buttoned" device which was developed in 1990 an d having succeeded in... |
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- Case Report
- A Case of Two Giant congenital Aneurysms of the Right Coronary Artery
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Yong Kwan Kim, Jo Won Chung, Jong Kyun Lee, Jun Hee Sul, Sung Kyu Lee
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Clin Exp Pediatr. 1994;37(6):850-853. Published online June 15, 1994
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Aneurysms of the coronary arteries are rare. They may be due to atherosclerosis, mucocutaneous lymph node syndrome, mycotic emboli, syphilis or trauma and occasionally they are congenital.
The prognosis appears to be poor and death can occur suddenly from rupture of the aneurysm, peripheral coronary embolism or bacterial endocarditis. Recently surgical treatment has been successful
In a 5 year old patient with... |
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- Original Article
- Morphological Classification of Left Superior Vena Cava and Analysis of Associated Cardiac Anomalies
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Eun Joo Choi, Jong Kyun Lee, Seok Min Choi, Jun Hee Sul, Sung Kyu Lee
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Clin Exp Pediatr. 1994;37(5):612-619. Published online May 15, 1994
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The persistend left superior vena cava(LSVC) is not rare cardiovascular developmental anomaly occurring both in association with congenital heart disdease and as an isolated anomaly of no hemodynamic importance. We have studied 73 cases of the LSCV out of 1,060 cases of congenital heart disease catheterized at Yonsei Cardiovascular Center.
We conducted the study with a view point of position of... |
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- Echocardiographic Evaluation of the Changes of the Interventricular Septal Morphology in Postoperative Tetralogy of Fallot Patients
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Im Jae Park, Jun Hee Sul, Jong-Kyun Lee, Seok Min Choi, Jo Won Chung, Sung Kyu Lee, Bum Koo Cho
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Clin Exp Pediatr. 1994;37(4):502-509. Published online April 15, 1994
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The hemodynamic feature of the tetralogy of Fallot (TOF) is best characterized by equality of left and right ventricular peak systolic pressure. The interventricular septum is flattened and thickened. Even after the right ventricular pressure is normalized in the postoperative period, the morphological abnormality continues for some time. We have analyzed the morphological changes of the IVS echocardiographically after total... |
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- Case Report
- A Case of congenital Diverticulum of Ventricle Associated with Pulmonary Atresia
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Kun Taek Kim, Jo Won Jung, Jong Kyun Lee, Jun Hee Sul, Sung Kyu Lee
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Clin Exp Pediatr. 1994;37(2):276-281. Published online February 15, 1994
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The congenital diverticulum of ventricle is a rare cardiac malformation arising from the left or right ventricle, the former being more common. Ventricular diverticulum is usually associated with other anomalies including intracardiac, midline thoracic, diaphragmatic and abdominal wall defect.
The authors experienced a case of congenital diverticulum of left ventricle in nine month-old female infant. Left Blolock-Taussig shunt operation was done... |
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- Original Article
- Morphlolgical Analysis of the Congenital Heart Disease Associated with Infrahepatic Interruption of IVC with Azygos Contnuation
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Jun Hee Sul, Jong Kyun Lee, Sung Kyu Lee
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Clin Exp Pediatr. 1993;36(4):543-549. Published online April 15, 1993
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Infrahepatic interruption of the inferior vena cava with azygos continuation is elatively infrequent cardiovascular developmental anomaly occurring both in association with congenital heart disease and as an isolated anomaly of no hemodynamic importance. During the past 5years, we observed 38cases of infrahepatic interruption of IVC with azygos continuation out of 2,397 cases of congenital heart disease catheterized at Yonsei... |
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- Tricuspid Atresia : A Re-evaluation and Classification
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Jun Hee Sul, Jong Kyun Lee, Seok Min Choi, Sung Kyu Lee
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Clin Exp Pediatr. 1993;36(12):1716-1720. Published online December 15, 1993
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Morphological evaluations accounting the associated anomalies were performed in the 60 cases of tricuspid atresia, diagnosed at Divsion of Pediatric Cardiology. The following results were obtained.
1) Twenty one out of the 6 cases had transposition of the great vessels, among which 8 cases were in complete A-transposition.
2) Seven cases were associated with pulmonany atresia, in 1 case, aorts arise from... |
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- Analysis of the Morphological Characteristics of Double Outlet Right Ventricle and Comparative Study of Operative Methods
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Jun Hee Sul, Jong-Kyun Lee, Jo Won Jung, Sung Kyu Lee, Bum Koo Cho
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Clin Exp Pediatr. 1993;36(12):1721-1731. Published online December 15, 1993
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Double outlet right ventricle, a complex of congenital cardiac anomalies in which both great arteries arise wholly or in large part from the morphologic right ventricle presents diverse clinical manifestations according to the morphological characteristics.
Eighty cases with DORV were diagnosed and operated at Yonsei Cardiovascular Center from 1988 to 1992. The analysis of the morphological characteristics of this anomaly and... |
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- Erratum
- Analysis of 5,653 Cases with Congental Heart Disease (CHD) Catheterized at Yonsei Medical Center - A 28-Year Review -
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Dong Shik Chin, Jong Kyun Lee, Jun Hee Sul, Sung Kyu Lee, Bum Koo Cho
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Clin Exp Pediatr. 1992;35(2):143-156. Published online February 15, 1992
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This is a 28-year analysis of 5,653 cases with congenital heart disease who underwent cardiac catheterization at Yonsei Medical Center from 1964 to 1991.
Form 1964, there was a steady increment in the number of catheterized cases with CHD until the late 1970's when the patients population began to increase rapidlly. This was undoubtedly set off by the introduction of the... |
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- Evaluation of Congenital Cardiac Anomalies Associated with Side by Side Ventricle
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Young Sook Kim, Jong Kyun Lee, Jun Hee Sul, Sung Kyu Lee, Dong Shik Chin
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Clin Exp Pediatr. 1992;35(2):168-173. Published online February 15, 1992
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Many forms of congenital heart disease are arrests in normal development. An understanding of the relevent embryology and pathology is basic to the understanding, accurate diagnosis, and successful management of congenital heart disease. The heart appears on the 18th day of life and its formation is normally completed by about the 40th day of life when the embryo is approximately... |
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- Clinical study on the factors used in the diagnosis of heart failure.
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Dong Chul Park, Seok Min Choi, Jun Hee Sul, Sung Kyu Lee, Dong Shik Chin
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Clin Exp Pediatr. 1991;34(11):1534-1539. Published online November 30, 1991
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Heart failure is the state in which heart cannot produce the cardiac output required to sustain the
metabolic needs of the body without evoking certain compensatory mechanisms. As these mecha-
nisms become ineffective, increasingly severe clinical manifestations result. The diagnosis of conges-
tive heart failure relies on several sources of clinical findings, including history, physical examination,
and chest X-rays. For lack of uniform diagnostic... |
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- A case of Gaucher's Disease Diagnosed by beta-Glucosidase Enzyme Deficiency.
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Hwan Gyn Park, Yil Sub Lee, Chang Hyun Yang, Chang Ho Hong, Sung Kyu Lee, Kyung Soon Song, Hyeon Joo Jeong
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Clin Exp Pediatr. 1990;33(4):514-521. Published online April 30, 1990
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We experienced a case of adult type Gaucher’s disease in a 2 year 9 month old female.
The patient had hepatosplenomegaly with anemia and characteristic Gaucher cells in bone marrow
aspiration and biopsy of liver and spleen.
Diagnosis was confirmed by demonstration of β-glucosidase enzyme deficiency in circulating
leukocytes.
Partial splenectomy was followed by improvement of anemia and thrombocytopenia. A brief
review of literature was done. |
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- Measles in Previously Vaccinated Children during Measles Epidemics.
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Hwan Gyu Park, Jeong Wan Yoo, Soh Yeon Kim, Young Mo Shon, Sung Kyu Lee, Kyung Soon Song
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Clin Exp Pediatr. 1990;33(11):1510-1515. Published online November 30, 1990
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A clinical study was made on 98 cases of measles patients admitted to YoungDong Severance
Hospital during the period of 7 months from June to December 1989. The patients with measles were
evaluated for presence of measles specific IgM antibody in serum, clinical symptom and vaccination
history.
We obtained the following results:
1) Out of 98 patients, 62 patients (63.3%) were vaccinated children and 36 patients... |
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- A Case of Mitral Atresia.
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Chang Yul Kim, Jun Hee Sul, Sung Kyu Lee, Dong Shik Chin
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Clin Exp Pediatr. 1989;32(3):418-422. Published online March 31, 1989
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Mitral atresia is a rare and fatal congenital heart disease.
We experienced a case of mitral atresia associated with double outlet right ventricle(S.D.S). atrial
septal defect and multiple ventricular septal defect in a 50 day old female infant. which was diagnosed
by echocardiogram and confirmed at autopsy. |
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- Studies of false tendon in left ventricle by echocardiography.
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Un Jun Hyoung, Jin Yong Lee, Jun Hee Sul, Sung Kyu Lee, Dong Shik Chin
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Clin Exp Pediatr. 1989;32(11):1503-1509. Published online November 30, 1989
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The False tendon is an anomalous chordae tendinae which attaches to abnormal sites in left
ventricle. We studied the incidence of false tendon and relationship of the false tendon, functional
murmur and arrhythmias using echocardiography.
The results were as follow;
1) We found false tendons in 42 cases of total 307 cases, 13.6%
2) In group I (the patients who have congenital heart disease), the incidence of... |
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- Truncus Arteriosus Associated with Interrupted Aortic Arch.
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Chang Hyun Yang, Jae Seung Yang, Jun Hee Sul, Dong Soo Kim, Sung Kyu Lee, Dong Shik Chin
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Clin Exp Pediatr. 1988;31(6):779-783. Published online June 30, 1988
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We experienced a case of truncus arteriousus associated with interrupted aortic arch, ventricular
septal defect and patent ductus arteriosus. A 5 month old boy had complained of rapid respiration and
feeding difficulty since birth.
There was no visible cyanosis or clubbing toes and nails. There was a grade 2 〜3 ejection systolic
murmur with maximum intensity at the left lower sternal border. Diagnosis was... |
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- Abdominal Ultrasonographic Findings in Patients with Kawasaki Disease.
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Ho Taek Kim, Chang Ho Hong, Chul Lee, Sung Kyu Lee, Pyung Kil Kim, Ki Kun Oh
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Clin Exp Pediatr. 1988;31(3):348-354. Published online March 31, 1988
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Kawasaki disease, first reported in Korea in 1973, is now one of the disease commonly encountered
in pediatric age group. It presents systemic symptoms including abdominal ones such as pain, nausea
and vomiting, etc. There have been several case reports of hydrops of the gallbladder occuring
concurrently with Kawasaki disease, and the abdominal symptoms of the disease are known to
correlate with hydrops of... |
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- A Case of Persistent Fetal Circulation.
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Jong Kyun Lee, Chul Lee, Ran Namgung, Sung Kyu Lee, Dong Gwan Han
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Clin Exp Pediatr. 1988;31(2):234-240. Published online February 28, 1988
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The authors have experienced a case of persistent fetal circulation associated with hypocalcemia.
The baby was delivered with full-term by repeated cesarean section. He showed marked dyspnea 4
hours after birth and thereafter cyanosis appeared. So artificial ventilator had been applied combined
with tolazoline administration. The patient was treated successfully and discharged on 28th hospital
day without complications.
We present one case of persistent fetal... |
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- Two-Dimensional Echocardiographic Diagnosis of Cornary Aneurysms in Children with the Mucocutaneous Lymphnode Syndrome.
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Jun Hee Sul, Sung Kyu Lee, Dong Shik Chin
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Clin Exp Pediatr. 1987;30(12):1363-1367. Published online December 31, 1987
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The two dimensional echocardiographic technique for detecting coronary artery aneurysms was
performed in 62 cases with mucocutaneous lymphnode syndrome. Of 62 patients with MCLS, coronary
artery aneurysms were detected as large echo-free space in 8 patients.
It was found that coronary artery aneurysms usually developed during the acute stage of the illness,
and regressed gradually thereafter. Most aneurysms disappeared in 6 months.
Therefore, Echocardiography is... |
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- The Criteria for Surgical Correction of Ventricular Septal Defect by Non-invasive Diagnostic Methods.
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Chuhl Joo Lyu, Jun Hee Sul, Sung Kyu Lee, Dong Shik Chin
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Clin Exp Pediatr. 1986;29(8):830-835. Published online August 31, 1986
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In selected cases, early corrective surgery is indicated in the management of infants with moderate or large ventricular septal defects. The risks of any surgical procedure in infancy are acknowledged to be great and should be avoided if possible. However, these surgical risks are justified when the patients have intractable congestive heart failure, marked growth retardation, recurrent prolonged lower respiratory... |
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- Case Report
- Coarctation of the Aorta : Unusual Type.
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Jung Bae Lee, Dong Soo Kim, Chuhl Joo Ryu, Kwang Sin Cho, Jun Hee Sul, Sung Kyu Lee, Dong Shik Chin, Kyu Ok Choe, Bum Koo Cho
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Clin Exp Pediatr. 1986;29(7):773-778. Published online July 31, 1986
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We experienced a case of coarctation of the aorta with aneurysmal dilatation which was
located in aortic arch, who was a 13 year old male.On physical examination on admission,
pulses were weak in right radial artery and in both femoral artery. Blood pressure measured 100/70 mmHg
in right arm, 100/70 mmHg in left arm, 130/110 mmHg in right leg and 130/110... |
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- A case of Unilateral Absence of Pulmonary Artery.
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Kwang Sin Joh, Dong Soo Kim, Chul Joo Ryu, Shin Heh Kang, Sung Kyu Lee, Ki Young Lee, Dong Shik Chin
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Clin Exp Pediatr. 1986;29(5):559-563. Published online May 31, 1986
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Unilateral Absence of Pulmonary Artery(UAPA) is a rare disease. It is characterized by no specfiic cardiopulmonary symptoms in general. We experienced a case of UAPA in a 9 year-old female patient with the chief complaint of abnormal chest Xray finding. Lung perfusion scan, cardiac catheterization with pulmonary and aortic angiography confirmed the diagnosis of right side UAPA.
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- Two cases of Vascular Ring.
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Jun Chul Choi, Dong Soo Kim, Jun Hee Sul, SUng Kyu Lee, Dong Shik Chin
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Clin Exp Pediatr. 1986;29(3):312-317. Published online March 31, 1986
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This study is a report of two cases of vascular ring that were experienced at Yonsei University in 1983 and 1985.
The first case was a one-month-old female patient with a double aortic arch and PDA.
The main pulmonary artery was connected to the anterior arch by PDA. The anterior arch was larger in diameter than the posterior arch and the descending... |
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- Original Article
- Aortography and Echocardiography by Countercurrent Injection Via Radial Artery in Newborns with PDA.
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Jun Hee Sul, Dong Kwan Han, Sung Kyu Lee, Dong Shick Chin
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Clin Exp Pediatr. 1986;29(11):1196-1200. Published online November 30, 1986
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Aortography and echocardiography by countercurrent injection into the radial artery performed for the detail diagnosis of PDA in newborns. The results were as follows：
1) Aortography by countercurrent injection via ridial artery affords an easy, safe and simple bedside means for
the diagnosis of PDA without retrograde arterial catheterization, which is occasonally complicated by thrombosis
of the artery in small infant.... |
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- Case Report
- A Successful Repair of Interrupted Aortic Arch.
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Dong Su Kim, Du Yung Lee, Jun Hee Sul, Sung Kyu Lee, Kyu Ok Choi, Bum Koo Cho, Dong Sik Chin
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Clin Exp Pediatr. 1983;26(4):386-391. Published online April 30, 1983
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This is a case report of Interrupted aortic arch combined with large ventricular septaldefect and patent ductus arteriosus. This 5 years old girl, she was complained of frequent upper respiratory infections, exertional
dyspnea from 6 months age. The diagnosis was confirmed by cardiac catheterization and angiocardiography.
Pressure of main pulmonary artery was 80/50 (63) mmHg, and that of descending aorta was 75/45(60)mmHg
(Qp... |
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- A Case of Pulmonary Infundibular Stenosis Developed in Ventricular Septal Defect.
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Boc Lyul Park, Jun Hee Sul, Sung Kyu Lee, Dong Shiek Chin
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Clin Exp Pediatr. 1983;26(2):175-179. Published online February 28, 1983
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I year 11 month old boy had large ventricular septal defect(Kirklin type I) with pulmonary hypertension and Eisenmenger syndrome, so operation was not indicated at that time. I year and 3month later pulmonary infundibular stenosis was developed and pulmonary artery pressure and resistence were decreased. Operation (patch repair) was performed successfully. A brief review of natural course of ventricular septal... |
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- Original Article
- Clinical Studies of Tetralogy of Fallot : Factors Affecting Outcome of Operation.
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Hong Jin Kim, Jun Hee Sui, Sung Kyu Lee, Dong shick Chin, Sung Nok Hong
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Clin Exp Pediatr. 1982;25(3):225-233. Published online March 31, 1982
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Tetralogy of Fallot is one of the most common cyanotic congenital heart disease. It consists of four features anatomically pulmonic stenosis or atresia, ventricular septal defect, overriding aorta, and right ventricular hypertrophy. One hundred and ninety one cases of Tetralogy of Fallot were confirmed by cardiaccatheterization at Severance Hospital. These were observed on general feature, cardiac catheterization findings and outcome... |
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- Case Report
- A case of Acute Renal Failure with Hemoglobinuria Following Open Heart Surgery.
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Jong Ho Kim, Jun Hee Sul, Sung Kyu Lee, Pyung Kil Kim, In Jun Choi, Bum Ku Cho
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Clin Exp Pediatr. 1980;23(9):724-729. Published online September 15, 1980
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Acute renal failure is a serious complication after open heart surgery which involve total body perfusion but the reported incidence of the complication has varied widely. We have experienced a case of acute renal failure with hemoglobinuria following an open heart surgery for correction of ventricular septal depect, which was comfirmed by cardiac catheterization. Kidney biopsy shows a typical change... |
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- Original Article
- Clinical Evaluation of 185 cases of Ventricular Septal Defect.
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Sung Kyu Lee, Pil Rai Chung, Jun Hee Sul, Dong Sick Chin, Duk Jin Yun
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Clin Exp Pediatr. 1980;23(6):446-457. Published online June 15, 1980
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One hundred and eighty nine cases of ventricular septal defect, which was confirmed by cardiac catheterization at Severance Hospital, were observed on clinical, hemodynamic, electrocardiogr sphic findings and their correlation, during the period from January, 1964 to December, 1979. The six hundred and forty one cases of congenital heart disease under fiften years old received cardiac catheterization during this period.... |
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- Clinical Studies on the Patent Ductus Arteriosus.
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Baek Keun Lim, Sung Kyu Lee, Duk Jin Yon, Seung Nok Hong
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Clin Exp Pediatr. 1980;23(10):798-808. Published online October 15, 1980
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Patent Ductus Arteriosus is one of the most common congenital heart diseases. The symptoms and clinical findings in patients with typical patnet ductus arteriosus are well recognized. That not all patient with ductus arteriosus have the typical clinical findings is well documented. Since the poor prognosis of untreated patent ductus arteriosus and good results of surgical intervention are fairly well... |
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- Case Report
- A Case of Uhls Anomaly.
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Jun Hee Sul, Ki Chun Kim, Ki Sub Chung, Sung Kyu Lee, Chang Jin Kim, Jae Yun Rho
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Clin Exp Pediatr. 1979;22(6):476-480. Published online June 15, 1979
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Congenital hypoplasia of the right ventricular myocardium, also known as parchment heart or Uhl's anomaly, is a rare congenital heart defect. It was first described in Oslers principles and Practice of Medicine in 1905 and reviewed by Segall We found 29 reported cases, but there was no reported case in Korea. Recently, we experienced a case of Uhls anomaly associated... |
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- Original Article
- Clinical Studies on Congenital Heart Disease (1964~1975).
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Suk Kyou Cha, Soo Hyung Kim, Seoc Koo Bai, Sung Kyu Lee, Dong Sik Jin, Hong Do Cha, Sung Soon Kim
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Clin Exp Pediatr. 1977;20(3):192-198. Published online March 31, 1977
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The clinical studies were performed on 757 patients who had been admitted to Severance Hospital from May, 1964 to June, 1975 with the diagnosis of congenital heart disease. The following results were obtained; 1. Among 757 patients, cardiac catheterization was performed on 367 patients. 2. Four hundred and thirty eight patients were male and 319 were female. Over half of... |
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- Clinical Studies on Guillain-Barre Syndrome (1969~1974)
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Soo Hyung Kim, Soo Young Whang, Sung Kyu Lee, Dong Shick Chin
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Clin Exp Pediatr. 1975;18(7):499-504. Published online July 31, 1975
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The clinical studies were performed on 58 patients who had been admitted to Severance hospital from Jaunary, 1969 to December, 1974 with the diagnosis of Guillain-Barre Syndrome. The following results were obtained:
1.Forty two cases were male and 16 cases female. The age ranged from 6 months to 43 years old with the peak incidence of 3 to 6 years. The... |
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- Case Report
- Ivemark’s Syndrome 4 Cases
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Soon II Lee, Woo Gill Lee, Bu Kyung Kang, Sun Hee Lee, Sung Kyu Lee, Dong Shik Chin, Duk Jin Yun
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Clin Exp Pediatr. 1975;18(6):468-472. Published online June 30, 1975
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Ivemark’s syndrome is rare disease and characterized by congenital absence of the spleen as sociated with characteristic group of anomalies of the cardiovascular and gastroenteric systems. We had experienced 4 cases of Ivemark’s yndrome: Case 1 had asplenia, situs inversus, dextrocardia, ASD, and pulmonary stenosis; Case 2 had asplenia, bilobulated liver, centraly located stomach but deviated to right side, single... |
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- Original Article
- A Clinical Study of Cerebral Palsy
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Soo Young Whang, Sung Kyu Lee
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Clin Exp Pediatr. 1975;18(2):128-134. Published online February 28, 1975
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This is a clinical study of 88 cerebral palsy cases, visited pediatric department of Severance Hospital from Feb. 1970 through Jun. 1974. We observed following results; 1)Spastic paralysis is 59 cases (67.0%) that subdevides into diplegia 26 cases (29. 6%), quadriplegia 25 cases (28.4%), paraplegia 5 cases (5.7%), hemiplegia 2 cases (2.3%), and monoplegia 1 cases (1.4%). Athetosis is 11... |
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- Case Report
- A Case of Congenital Cleft Sternum
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Kwang Soo Sohn, Woo Gill Lee, Joon Tai Kim, Sung Kyu Lee, Duk Jin Yun
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Clin Exp Pediatr. 1975;18(10):771-773. Published online October 31, 1975
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Bifid sternum is a congenital midline malformation resulting from disturbance of normal fusion and the defects allows a herniation of the pericardium covered only by the subcutaneous tissue and skin. A case of congenital cleft sternum in 8 month old male infant was presented. There was marked paradoxical motion with respiration in the area of the defect and a long... |
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- Original Article
- A Clinical Study of Trachoestomy and It’s Complication in Infant and Children
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Soon Hi Lee, Young Soon Lee, Sung Kyu Lee, Dong Shick Chin, Duk Jin Yun
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Clin Exp Pediatr. 1974;17(4):278-283. Published online April 30, 1974
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A total of 33 children with tracheostomy were observed after admission in Severance Hospital
during the past 10 years and 3 months from January 1958 to March 1973.
1. Sex incidence was 20iiiale to 13female, and complications occured in 17 cases.
2. The age and complication rate relationship showed that about 70% of the patients were under
5... |
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- Case Report
- A Case of Epidermolysis Bullosa Hereditaria
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Myung Suk Kim, Young Soon Lee, Sung Kyu Lee, Duk Jin Yun, Chung Koo Cho, In Joon Choi
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Clin Exp Pediatr. 1974;17(2):168-171. Published online February 28, 1974
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Epidermolysis bullosa hereditaria is an uncommon skin disease which is manifest at birth or
in infancy. It is characterized by blister formation occuring spontaneously or after friction or
slight trauma. Recently, we experienced a case of epidermolysis bullosa hereditaria in one day old newborn
infant, who was developed bullae on the neck, abdomen, both extremities and buttock.
A brief review of literature was made.
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- Original Article
- A Comparative Study on Growth of Infants Cared for in Well Baby Clinic and Milk Station
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Sung Kyu Lee
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Clin Exp Pediatr. 1969;12(3):121-136. Published online March 31, 1969
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Growth is a manifestation of life in the young and its rate and quality are importantly related to
the general health and welfare of the individual. Because of this important relationship, parents and
pediatrician must have intimate knowledge of the phenomenon of growth.
Infancy is the period of most rapid extrauterine growth.
There are factors influencing growth such as genetic factors, trauma, nutritional factors,... |
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- Clinical Studies on Guillain-Barre Syndrome in Children (1964〜 1968)
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Sung kyu Lee, Sang Hoo Park, Jae Sung Lee, Duk Jin Yun
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Clin Exp Pediatr. 1969;12(3):137-142. Published online March 31, 1969
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This paper presents the clinical study of 31 cases under 15 years of age who had been admitted to
Severance Hospital and Wonju Union Christian Hospital from January, 1964 to December, 1968
with the diagnosis of Guillain Barre syndrome.
1. Twenty one cases were male and 10 cases female. The age ranged from 3 months to 15 years
with the peak incidence of 3 to... |
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