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- Original Article
- Percutaneous Balloon Valvuloplasty in Children with Pulmonary and Aortic Valvular Stenosis.
- Chan Uhng Joo, Jung Soo Kim, Ho Yunh Song
- Clin Exp Pediatr. 1989;32(9):1224-1231. Published online September 30, 1989
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Pulmonary and aortic valvular stenosis were relieved by percutaneous balloon valvuloplasty during cardiac catheterization on 14 children aged 22 months to 18 years. Before dilatation the transpulmonary systolic pressure gradients ranged from 43 mmHg (mean 87. 8 mmHg) in children with pulmonary valvular stenosis. There were significant reduction in the transpulmonary systolic pressure gradient (mean 33.1 mmHg) immediately after balloon valvuloplas- ty except one patient... -
- Post-Exercise Pulmonary Function Changes in Asthmatic Children.
- Kyung Ae Yoon, Young Yull Koh, Hyung Ro Moon
- Clin Exp Pediatr. 1989;32(8):1074-1085. Published online August 31, 1989
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To determine the frequency, severity, time course and relations of exercise induced changes in lung function, forty-one asthmatic children and fifteen control children were subjected to free running and forced vital capacity (FVC), one-second forced expiratory volume (FEV1), maximum mid-expiratory flow rate (FEF 25-75%), and peak expiratory flow rate (PEFR) were measured before and serially for 60 minutes following exercise. The results were as follows. 1) Significant... -
- Continous Wave Dopple Echocardiographic Prediction of Pulmonary Arterial Hupertension in Congenital Heart Disease.
- Jung Suk Lee, Mi Jung Ko, Yeon Gyun Oh, Hyang Suk Yoon
- Clin Exp Pediatr. 1989;32(7):951-957. Published online July 31, 1989
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This study determines the accuracy of Doppler echocardiography for predicting the presence of pulmonary artery hypertension from Doppler pulmonary artery velocity traces. The patient group included 26 patients with congenital cardiac disease who had undergone catheterization. Doppler measurements of acceleration time(AT), right ventricular ejection time (RVET), and AT/ RVET were compared with pulmonary artery pressure (PAP) and mean pulmonary artery pressure (m-PAP). We devided the patients in... -
- Comparisons of the Ratio of Pulmonary to Systemic Blood Flow(Qp/Qs) Determined by Non-invasive Doppler Echocardiography and Radionuclide-Angiocardiography in Congenital Heart Diseases.
- Jung Suk Lee, Chul Wo Park, Hyang Suk Yoon
- Clin Exp Pediatr. 1989;32(7):943-950. Published online July 31, 1989
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This study was desinged to assess the accuracy of the ratio of pulmonary to systemic blood flow (Qp/Qs) measured by non-invasive continuous wave (CW) Doppler echocardiography comparing with other non-invasive Radionu- clide Angiocardiography (RNA) and invasive Fick method. Seventeen children with congenital heart disease, aged 14 months to 15 years, admitted for cardiac opention to this hospital, were studied. High correlations were found between the... -
- Expected Normal Values of Pulmonary Function test in Pediatric Age 1.by Spirometry.
- S Y Yang, M J Na, W H Choi, K W Kim
- Clin Exp Pediatr. 1989;32(2):206-214. Published online February 28, 1989
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Pulmonary function test is essential not only to find out the conditions of pulmonary desease such as asthma and determine the drug effects but also to diagnosis various diseases through the provocation tests or the elimination tests which are taken by foods, drugs, exercises or various kinds of antigens. With the total 531 cases, among them 277 boys and 254 girls who are... -
- Noninvasive Estimation of Pulmonary Artery Pressure with Doppler Echocardiogrphy.
- Ji Yean Lee, Soon Hak Kwon, Sang Bum Lee, Doo Hong Ahn
- Clin Exp Pediatr. 1989;32(1):20-26. Published online January 31, 1989
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This study determined the accuracy of Doppler echocardiography for predicting the pulmonary artery pressure from right ventricular systolic time intervals in 25 pediatric patients with various congenital cardiovascular diseases undergoing cardiac catheterization. Either estimated pulmonary artery systolic pressure (PASP) using Burstin nomogram and pulmo- nary artery diastolic pressure (PADP) using Riggs equation (PADP= 151· RPEP / RVET ·20.7) correlated well with the pressures at... -
- A Case of Pulmonary Squestration.
- Byung Sook Park, Jin Oh Kim, Beyong Sang Choi, Chan Uhng Joo, Dae Yeol Lee
- Clin Exp Pediatr. 1988;31(10):1390-1393. Published online October 31, 1988
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Pulmonary sequestration is an uncommon congenital malformation charcterized by the presence of nonfunctioning lung tissue which usually has no communciation with the normal bronchial tree and which receives it's blood supply from an anomalous systemic artery instead of pulmonary arterial branch. We have experienced a case of pulmonary sequestration. The patient was 5 10/12 years old girl with the complaint of fever, cough, Chest films... -
- 4 Cases of Non-Hematogenous Disseminated Pulmonary Tuberculosis.
- Mi Ja Yoon, Myung Soo Chang, Bok Lyun Kim, Shin na Kim, Hae Soon Chang
- Clin Exp Pediatr. 1988;31(9):1225-1231. Published online September 30, 1988
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Unlike hematogenous spread in miliary tuberculosis, disseminated pulmonary tuberculosis is considered to be spread by non-hematogenous transbronchial with characteristic chest X-ray appear- ance. This type of spread is unusal in childhood pulmonary tuberculosis. We are reporting 4 such cases from 1984 to 1986 with chest X-ray findings. In city hospital where most patients come from low-income families, we see significant number of children with various types... -
- Two Cases of Idiopathic pulmonary Hemosiderosis.
- Sung Ky You, Ki Soo Kim, Young Jee Kim, Young Yull Koh, Yeon Lim Suh, Je Geun Chi
- Clin Exp Pediatr. 1988;31(9):1209-1216. Published online September 30, 1988
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Idiopathic pulmonary hemosiderosis is an uncommon disease of undetermined cause that is char- acterized by periodic episodes of cough, hemoptysis, widespread pulmonary infiltrates and hypo- chromic anemia. Two cases of idiopathic pulmonary hemosiderosis were diagnosed after open lung biopsy. It revealed hemosiderin and hemosiderin-laden macrophage. There were no specific causes for pulmo- nary hemorrhage. We report 2 cases of idiopathic pulmonary hemosiderosis with brief review... -
- Noninvasive Estimation of Systemic and Pulmonary Blood flow and the Ratio of Pulmonary to Systemic flow by Two-Dimensional Doppler Echocardigraphy.
- Woo Tack Kim, Ki Ho Kim, Haeng Mi Kim, Snag Bum Lee
- Clin Exp Pediatr. 1988;31(7):881-891. Published online July 31, 1988
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This study was designed to assess the accuracy and problems of noninvasively measuring right and left cardiac output at various sampling sites by range gated pursed Doppler echocardiography. High correlations were found between Fick-and Doppler-derived measurements of systemic and pulmonary flow as well as the pulmonary to systemic flow ratio in 21 patients undergoing cardiac catheterization (systemic flow [n=21] r=0.81; plulmonary flow [n=29], r=0.78;Qp/Qs... -
- Percutaneous Transluminal Balloon Valvuloplasty for Congenital Pulmonary Valve Stenosis.
- Heung Jae Lee, Jae Kon Ko, Woong Heum Kim, Nam Su Kim, Chang yee Hong
- Clin Exp Pediatr. 1988;31(7):822-832. Published online July 31, 1988
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During the period of 2 years, between January 1986 and December 1987, 36 patients, aged 2 years to 18 years, with congenital pulmonary valve stenosis(PVS) (with peak systolic transvalvar gradient over 30 mmHg) underwent percutaneous transluminal balloon valvuloplasty(TBV) at Sejong General Hospital m Korea. Of a group of 36 patients, 26 were treated successfully by the conventional balloon valve dilatation technique, and 6 were treated... -
- Doppler Echocardiographic Determination of the Time of Ductal Closure in Normal Newborn Infants.
- Dong Joo Na, Hyung Kook Kim, Jong Wan Kim, Sang Min seong, Kyong Su Lee, In Soo Park
- Clin Exp Pediatr. 1988;31(6):747-753. Published online June 30, 1988
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Pulsed Doppler echocardiography, a sensitive and specific non-invasive method enabled the various congenital and acquired heart diseases to be detected sine 1970，s For determining the time of functional closure of ductus arteriosus, 30 normal newborn infants were examined by pulsed wave Doppler (PWD) from March 1 to April 30, 1987, in Holy Family Hospital, Catholic Medical Center. A PDA was diagnosed when abnormal diastolic ductal... -
- A Case of Pulmonary Candidiasis.
- Hye Ran Byun, Kung Ha Ryu, Moon Ja Kim, Keun Lee, Yeon Lim Suh, Je Geun Chi
- Clin Exp Pediatr. 1988;31(5):621-626. Published online May 31, 1988
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A case of fatal pulmonary candidiasis was diagnosed at autopsy of 5-month-old female infant. Patient had mild coughing, poor weight gain and marked hepatosplenomegaly. She had no sign of immune dysfunction but developed fever, wheezing and intermittent respiratory distress. Chest P-A showed infiltrations of multiple lobar pneumonia. Postmortem examination revealed the whitish necrotic mass like lesion with a feature of lobar pneumonic consolidation in... -
- A Case of Pulmonary Paragonimiasis Whose Parenchymal Lesions Dtected by Tomogram and Perfusion Scan of the Lung.
- Jung Keun KIm, Kyu Earn Kim, Ki Young Lee
- Clin Exp Pediatr. 1988;31(4):519-525. Published online April 30, 1988
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Recently, we experienced a case of pulmonary paragonimiasis in a 8 year old boy with a chief complaint of intractable pleural fluid for one year. The cystic cavity was detected by tomogram, but not by chest X-ray and apparant regional pulmonary perfusion defect was also detected at the same site of that lesion by lung scan. We report this case with brief review of... -
- The Case of Persistent Pulmonary Hypertension of the New born.
- Sung Oh Kim, Soo Yup Lee, Kyoo Hwan Lee, Soo Jee Moon
- Clin Exp Pediatr. 1988;31(1):128-133. Published online January 31, 1988
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Persistent pulmoanry hypertension of the newborn (PPHN) is a syndrome consisting of severe hypoxemia and pulmoanry hypertension that appears within hours of birth. The essential pathophysiologic features of this syndrome is pulmonary artery hypertension causing right-to-left shunt through the patent ductus arteriosus or foramen ovale or both and clinically manifested by central cyanosis and respiratory distress. We recently have experienced 20 hour old female and... -
- Percutaneous Balloon Angioplasty in Children with Pulmonary Valvular Stenosis.
- Yong Soo Yun, Chang Yee Hong
- Clin Exp Pediatr. 1987;30(12):1355-1362. Published online December 31, 1987
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Pulmonary valve stenosis was relieved by balloon dilatation during cardiac catheterization on 58 children aged 8 months to 15 years, mean 6.2 years. Pulmonary valve diameter was estimated by two-dimensional echocardiogrphy to assist in the choice of balloon size. Before dilatation the transpulmonary systolic pressure gradients ranged from 15 mmHg to 250 mmHg. There were significant reduction in the transpulmonary systolic pressure gradients immediately after... -
- Pulmonary Air Leaks in the Newborn.
- Myung Chul Cho, Beyong Il Kim, Son Moon Shin, Jung Hwan Choi, Chong Ku Yun
- Clin Exp Pediatr. 1987;30(7):727-734. Published online July 31, 1987
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A clinical study was performed on 17 cases of pulmonary air leaks in the newborn who were admitted to the NICU of SNUH from Jan. 1980 to Jun. 1986. The results were as follows: 1) Spontaneous air leaks were 2 cases (11.8%) and secondary air leaks were 15 cases (88.2%). 2) Of the 17 cases of pulmonary air leaks, 9 cases (53.0%) were premature infants, 10... -
- A Case of Pulmonary Lymphangiectasis Associated with Chylothorax.
- Min Hee Kim, Jae Kyoung Lee, Oh Bae Chun, Byoung Hoon Yoo, Jae Hyung Yoo
- Clin Exp Pediatr. 1987;30(4):422-426. Published online April 30, 1987
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Congenital pulmonary lymphangiectasis is a rare abnormality usually becoming manifest at birth and almost invariably fatal in neonatal period or early infancy. Chylothorax is an infrequent manifestation of this disease. We report a patient with pulmonary lymphangiectasis, 3 year old male, who had been suffered from persistent respiratory distress since 7 days after birth, in whom the diagnosis was suggested by the appearance of... -
- Case Report
- A Case of Subdiaphragmatic Total Anomalous Pulmonary Venous Return.
- Ho Jin Lee, Sung Sik Lee, Soon Il Lee, Young Seok Lee, Je Geun Chi
- Clin Exp Pediatr. 1986;29(7):791-796. Published online July 31, 1986
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One case of subdiaphragmatic total anomalous pulmonary venous return in a newborn male baby under the impression of respiratory distress syndrome was presented. Isolated form of subdiaphragmatic total anomalous pulmonary venous return was confirmed by autopsy. The pulmonary veins joined a common trunk which was connected to the hepatic vein below the diaphragm for the venous circulation. There were two associated small... -
- A case of Unilateral Absence of Pulmonary Artery.
- Kwang Sin Joh, Dong Soo Kim, Chul Joo Ryu, Shin Heh Kang, Sung Kyu Lee, Ki Young Lee, Dong Shik Chin
- 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. -
- Original Article
- Post-exercise Pulmonary Function Changes in Asthmatic Children.
- Hee Joo Jeon, Jong Woo Shin
- Clin Exp Pediatr. 1986;29(4):353-360. Published online April 30, 1986
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The pulmonary function tests were made after exercise provaction using bicycle in 22 :asthmatic and 6 healthy children. The results obtained were summarized as follows: 1) There was no significant difference in pre-exercise pulmonary function tests between asthmatic and control children. 2) Among 22 asthmatic children, 17-10 children(77.3%~45.5%) according to different test indices, showed significant air way obstruction after exercise. 3) In the time... -
- Case Report
- A Case of Pulmonary Arteriovenous Fistulas with Cyanosis.
- Yun Oak Rho, Hyun Eog Yang, Kyong Su Lee, Kyung Sub Shin
- Clin Exp Pediatr. 1986;29(3):327-331. Published online March 31, 1986
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Pulmonary arteriovenous fistula is a congenital vascular malformation in lung resulting from abnormal capillary development and thus unoxygenated, desaturated arterial blood enters into the pulmonary venous system and results in various symptoms such as exertional dyspnea, cyanosis, clubbing fingers and secondary polycythemia. The exact etiology of pulmonary arteriovenous fistula is not well known but it may occur with or without hereditary... -
- A Case of Cryptococcosis with Advanced Pulmonary Tuberculosis.
- Hi Ju Park, Yong Joon Kim, Sang Kun Jung, Chan Yung Kim
- Clin Exp Pediatr. 1986;29(1):95-100. Published online January 31, 1986
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This is a case of cryptococcosis accompanied by pulmonary tuberculosis and malnutrition. The 11-year-old female patient was admitted to our hospital because of dyspnea, ascites and oliguria. Cervical lymph node biopsy and chest X-ray were checked, which were revealed tuberculous lesions. She was treated with amphotericin-B for 10 weeks, but didn*t complete remission at present. -
- Pulmonary Sequestration.
- J M Ryu, K A Ree, C H Yoon, S H Choi, K G Cho
- Clin Exp Pediatr. 1985;28(6):593-596. Published online June 30, 1985
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The pulmonary sequestration is an uncommon congenital anomaly characterized by the presence of a part of lung tissue which is supplied by an aberrent artery from the aorta or its branch and usually has no communication with the normal bronchial tree. This is a relatively uncommon anomaly that requires arteriography for definitive diagnosis. We have experienced one case of pulmonary... -
- Original Article
- Pulmonary Infiltration in Rotaviral Gastroenteritis.
- Wan Sup Kwak, Wang Bock Lee, Haeng Mi Kim, Ja Hoon Koo
- Clin Exp Pediatr. 1985;28(5):448-454. Published online May 31, 1985
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A clinical study was conducted to determine the frequency and degree of pulmonary infiltration in patients with rotaviral gastroenteritis. Thirty-three children with Rotazyme test positive gastroenteritis were enrolled in the study group, who had been admitted to the Pediatric Department of Kyungpook National University Hospital from September, 1983 to December, 1983. The following results were obtained: Vomiting and signs/symptoms of... -
- Peumomediastinum in the Newborn.
- Dong Gwan Han
- Clin Exp Pediatr. 1985;28(3):217-224. Published online March 31, 1985
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A retrospective review was performed of 15 medical records to study the pneumomedia- stinum in the newborn during last 4 years from Jan. 1980 through Dec. 1983 at Severance Hospital of Yonsei University. Tne results were as follows： 1) The incidence was 0.14% (15 of 8,737 live-births) during the neonatal period. Of those cases spontaneous pneumomediastinum was 66.7%(10 cases) and secondary pneumomedia- stinum 33.3%(5 cases). Males were... -
- Case Report
- A case of Idiopathic pulmonary hemosideroisis.
- Yeong Hee Kim, Jeong Hee Lee, Seung Joo Lee, Keun Lee, Ok Kyung Kim, Doo Yeon Lee
- Clin Exp Pediatr. 1985;28(2):182-186. Published online February 28, 1985
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Idiopathic Pulmonary Hemosiderosis is a rare disease characterized by recurrent attacks of hemoptysis, iron deficiency anemia and pulmonary infiltration on chest X-ray. We experienced a case of Idiopathic Pulmonary Hemosiderosis in a 3 year-old boy with recurrent attacks of dyspnea, pallor and chest infiltration on X-ray, without underlying pulmonary disease. Diagnosis was established by hemosiderin and hemosiderin-laden macrophage on lung... -
- Original Article
- Secondary Pneumothorax in the newborn.
- Dong Gwan Han
- Clin Exp Pediatr. 1985;28(2):123-130. Published online February 28, 1985
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Clinical records of 25 neonates with secondary pneumothorax were reviewed retrospectively during last 6 years from Jan. 1978 through Dec. 1983 at Pediatric Department of Yonsei University Hospital. The following results were obtained; 1)The incidence of secondary pneumothorax was 0.16% (21 out of 12,864 live-birth) during the neonatal period. The incidence tended to increase since we had set up the neonatal,... -
- Echocardiographic Evaluation of Pulmonary Arterial Hypertension in Pediatric Congenital Heart disease.
- Myoung Sung Moon, In Hee Park, Heung Jae Lee, Hahng Lee, Keun Soo Lee
- Clin Exp Pediatr. 1984;27(10):971-981. Published online October 31, 1984
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To assess the validity of Echocardiographic criteria for pulmonary arterial hypertension we studied pulmonary valve motion in 75 congenital heart disease children. 75 patients were divided into two groups, A and B. The group A consisted of 39 patients who had normal pulmonary arterial pressure, group B consisted of 36 patients who had pulmonary arterial hypertension(pulmmonary artery mean pressure more... -
- Case Report
- Two Cases of Anomalous Origin of the Right Pulmonary artery from the Ascending Aorta.
- Kyu Gap Hwang, Gu Soo Kim, Jung Yun Choi, Yong Soo Yun, Chang Yee Hong
- Clin Exp Pediatr. 1984;27(5):501-505. Published online May 31, 1984
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Anomalous origin of one pulmonary artery from the ascending aorta is a rare congenital malformation. It happens as the result of abnormal development of the 6th aortic arch. Anomalous origin of right pulmnary artery is more frequent than left. It is frequently associated with P.D.A., V.S.D. and T.O.F. In this malformation, congestive heart failure develops in early life and once the... -
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