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Case Report
Case of Chronic Pancreatitis Complicated Pancreatic Ascites and Pleural Effusion.
Gye Ja Lee, Yong Aee Chun, Hey Sun Lee, Yong Mi Hong, Young Min Ahn
Clin Exp Pediatr. 1987;30(1):108-113.   Published online January 31, 1987
A case of pancreatic ascites and pleural effusion as complication of chronic pancreatitis in the twelve-year-old boy was reported. He was admitted to the pediatric ward with chief complaints of abdominal pain and abdominal distension. He has been apparently well until one month prior to admission, when he began to feel intermittent abdominal pain and dyspnea and his abdomen was progressively distended. Serosanguinous fluid was...
Two Cases of Nephropathy in Association with Acute Rheumatic Fever.
Young Hi Park, Myoung Su Chang, Mi Ja Yoon, Shinna Kim
Clin Exp Pediatr. 1987;30(1):102-107.   Published online January 31, 1987
Two cases of nephropathy in association with acute rheumatic fever are presented. Both patients had Rheumatic carditis with mitral valvular involvement and positive urinary laboratory findings of significant hematuria and proteinuria. There was no relapse of nephropathy after initial recovery and both patients are getting monthly injection of Benzatine-penicillin as prophylaxis to prevent recurrence of rheumatic fever.
Original Article
Juvenile Chronic Lymphocytic Thyroiditis.
Duk Hi Kim
Clin Exp Pediatr. 1987;30(1):71-79.   Published online January 31, 1987
A diagnosis of chronic lymphocytic thyroiditis(CLT) was made in 90 children & adolescents according to Fisher’s criteria. The age of the group ranged between 4 years & 16 years. On the basis of serum T4, T3 & TSH, three groups of patients were distinguished at the time of diagnosis.: euthyroid group (n=49), hyperthyroid group (n=7), hypothyroid group (n=34), where three subgroups were classified;...
Clicical Syudy on Cardiac Involvement in Rheumatic Heart Disease in Children.
Sung Ho Cha, Myeong Yeon lee, Jong Woo Bae, Byeong Soo Cho, Chang Il Ahn
Clin Exp Pediatr. 1986;29(11):1215-1224.   Published online November 30, 1986
A clinical study was carried out to obtained the cardiac manifestations and echocardiographic findings from 25 cases of rheumatic carditis, those were undertaken echocardiography among 52 cases of rheumatic carditis from January 1973 to June 1985, admitted to Pediatric department of Kyung Hee university hospital. And compared with age matched 14 cases of control group. The following results were obtained: 1)...
Case Report
A Case of Potter Syndrome Type I.
Jong Cheol Ryu, Jae Kwang Hong, Jun Taek Park, Jung Sik Min, Chang Jee Choi, Je Geun Chi
Clin Exp Pediatr. 1986;29(10):1152-1156.   Published online October 31, 1986
We have experienced a case of Potter syndrome type I in a newborn infant who presented with severe respiratory distress soon after birth. The diagnosis was made with autopsy findings consisted of bilateral polycystic renal dysplasia, bilateral hypoplastic lung , facies renalis, fibrocystic change of liver, patent ductus arteriosus, patent foramen ovale, ureter and urinary bladder hypoplasia and calcaneovarus. Brief...
A Case of Infantile Cortical Hyperostosis.
Young Bin Cho, Gyu Ho Lim, Young Choon Woo, Ki Yang Ryoo
Clin Exp Pediatr. 1986;29(9):1035-1040.   Published online September 30, 1986
Infantile cortical hyperostosis occurs in the first few months of life, and is characterized by hyperirritability, swellings of the soft tissues, and cortical thickenings of the underlying bones. It's cause is unknown. Recently we experienced a case of infantile cortical hyperostosis in a 2 month old male infant, who complained of irribility, anorexia, swellings and bowing deformities of the lower limbs. The diagnosis...
Original Article
A Study on Hormonal Change of Lh, FSH, and Testosterone and Testicular Volumes in Pubertal Mal Children.
Heung Dong Kim, Duk Hi Kim, Ki Keun Oh
Clin Exp Pediatr. 1986;29(9):979-987.   Published online September 30, 1986
The mechanism involved in pubertal changes has not been clearly demonstrated, but evidence has been accumulated that hormonal changes are responsible for this pubertal changes. We studied the height, weight, testicular volume, bone age, LH, FSH, and testosterone, "by Tanner stage of pubic hair development in 134 pubertal male children with no previous endocrine disease, who admitted at Yonsei University Medical...
Case Report
A Case of Autoimmune Hemolytic Anemia Caused by Warm Antibody.
Sei Hee Choi, Mee Kyung Namgoong, Baek Keun Lim
Clin Exp Pediatr. 1986;29(8):898-901.   Published online August 31, 1986
We reviewed a case of autoimmune hemolytic anemia caused by warm antibody in 7years old male patient. Diagnosis was established by clinical features, physical findings, laboratory findings, such as, CBC, Coombs’ test, fragility test, and bone marrow aspiration. Literatures were briefly reviewed.
Original Article
A Clinicopathological Study on Re nal Biopsies in Children.
Soon Wha Kim, Keun Chan Sohn
Clin Exp Pediatr. 1986;29(8):868-879.   Published online August 31, 1986
A clinical and histopathologic study was made on 80 cases of renal biopsies in children who were admitted to National Medical Center from January 1976 to June 1985. The results are as follows: 1) Among 80 cases, 60 cases were male and 20 cases female. The sex ratio of male to female was 3 : 1. The age distribution was from...
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
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...
Adrenal Cortical Adenoma Associated with Spinal Epidural Lipomatosis and Paraplegia.
Il Whan Kim, Chul Hoe Koo, Jae Sun Park, Sung Uhn Baek, Sung Do Lee, Kyu Ho Lee, Jae Do Kim, Bang Hur, In Sun Jun
Clin Exp Pediatr. 1986;29(7):784-790.   Published online July 31, 1986
A 14 year old girl was admitted because of severe obesity, respiratory difficulty and weakness of legs with edema. Diagnosis of Cushing* s syndrome by left adrenal adenoma was made by hormonal assay, abdominal C-T and surgery. 1 week after adrenalectomy, she developed paraplegia which was caused by massive deposition of fat in the spinal epidural space and compression of thoracic spinal cord. She was...
Original Article
A Study on Plasma Antidiuretic Hormone and Serum Sodium Levels of Cord Blood in the Newborn Infants.
Choon Ho Park, Chang Soo Ra
Clin Exp Pediatr. 1986;29(7):748-757.   Published online July 31, 1986
The authors studied the plasma antidiuretic hormone levels of cord blood in 40 cases of newborn infants and also studied the serum sodium levels of cord blood in 40 cases of newborn infants. For the purpose of analysis, the study subjects were divided into four group; 1st group of 17 cases of vaginal delivery infants with fetal distress, 2nd group...
Idiopathic IgA Nepropathy in Children.
Hae Il Cheong, Han Wook Yoo, Kwang Wook Ko
Clin Exp Pediatr. 1986;29(6):633-643.   Published online June 30, 1986
We analyzed clinical findings, pathological findings and clinico-pathological correlations in 55 children with idiopathic IgA nephropathy confirmed immunopathologically, and the results were as follows; 1) The mean age at onset was 9.65±2.45 years with relatively even distribution in school ages and males outnumbered females by 1.75 : 1. 2) The main mode of presentation was typical...
Clinical Observation of Rheumatic Fever and Rheumatic Heart Disease in Children.
Soon Don Hong, Sung Ho Cha, Chang Il Ahn
Clin Exp Pediatr. 1986;29(6):596-603.   Published online June 30, 1986
Acute rheumatic fever is an inflammatory disease of the heart, joint, central nervous system, and subcutaneous tissues which developes after a nasopharyngeal infection by group A beta-hemolytic Streptococci. Rheumatic fever is especially important to pediatrician because of the most acquired heart disease which usually ensues. To analyze the 101 cases of rheumatic fever and rheumatic heart disease in pediatric department of...
Case Report
Three Cases of Familial Glucocorticoid Deficiency.
Soo Heum Lim, Young Wun Kim, Byoung Hai Ahn, Hyung Ro Moon
Clin Exp Pediatr. 1986;29(5):549-552.   Published online May 31, 1986
Familial glucocorticoid defiency is a form of chronic adrenal insufficiency which is characterized by isolated deficiency of glucocorticoid and elevated levels of corticotropin in association with normal aldosterone production. It is thought to be degenerative process of adrenal cortex, with autosomal recessive or X-linked recessive pattern of inheritance. Skin hyperpigmentation and hypoglycemic symptom are characteristic and salt-losing symptom doesn’t develop....
Two Case of Infantile Cortical Hyperostosis.
Hae Lim Chung, Heon Seok Han, Young Yull Koh, Yong Seung Hwang, kyung Mo Yeon
Clin Exp Pediatr. 1986;29(4):441-445.   Published online April 30, 1986
We experienced 2 cases of Infantile Cortical Hyperostosis. Case I was 2V2 month old male who complained of irritability and tender swelling on extremities. Case I was 3 month old male who complained of deformities in both legs and irritability on handling above lesions. The diagnosis was established by typical clinical findings and radiological evidence A brief review of...
Original Article
Progostic Factors in Neonatal Asphyxia.
Hye Li Chung, Wan Sup Kwak, Haeng Mi Kim, Doo Hong Ahn
Clin Exp Pediatr. 1986;29(4):420-425.   Published online April 30, 1986
A clinical study was conducted on 30 term babies with neonatal asphyxia, who were admitted to Pediatric Department of Kyungpook National University Hospital during 2years period from May 1983 to April 1985. Of the 20 cases returned to follow up, 15 cases were neurodevelopmentally normal but 5 cases were retarded with neurologic disability. Retarded case revealed higher incidence of severe asphyxia...
Case Report
Two cases of Vascular Ring.
Jun Chul Choi, Dong Soo Kim, Jun Hee Sul, SUng Kyu Lee, Dong Shik Chin
Clin Exp Pediatr. 1986;29(3):312-317.   Published online March 31, 1986
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...
Original Article
The Clinical Study of Rodenticide Intoxication in Children.
Song Yee Koh, Myoung Ho Kang, Byoung Tae Kim, Dong Hong Ahn, Sang Jhoo Lee
Clin Exp Pediatr. 1986;29(3):305-311.   Published online March 31, 1986
A clinical study on 34 cases with rodenticide intoxication seen at Soon Chun Hyang College Hospital from January, 1979 to July, 1984 was performed. The results were as follows: 1) The rodenticide intoxication accounted for 20% of all drug intoxication. Fluoroacetate intoxication 24 cases (70.6%), vacor intoxication 1 cases (2.9%), phosphorus 及 arsenic into xication none and unknown rodenticide intoxication 9 cases...
Case Report
Two Cases of Hemolytic Disease of Newborn due to Anti-E.
Se Won Park, Young Sun Kim, Jung Hwan Choi, Hyo Seop Ahn, Chong Ku Yun
Clin Exp Pediatr. 1986;29(2):203-208.   Published online February 28, 1986
Isoimmune hemolytic disease of the newborn is a disease which is caused by maternal sensitization to one of the fetal blood factors. This report presented two esses of isoimmune hemolytic disease due to anti-E in 2 male newborns who were admitted to Seoul University Hospital because of jaundice. Antibody screening and antibody identification tests were made which revealed anti-E antibody...
Original Article
Clinical Study of Therapeutic Effect in Status Epilepticus.
Young Hyuk Lee, Chang Jun Coe
Clin Exp Pediatr. 1986;29(1):72-78.   Published online January 31, 1986
A clinical studies were conducted to determine the effectiveness of anticonvulsant treatment in 90 cases of status epilepticus in children who had been admitted to Pediatric Department of Yonsei University Medical Center from January 1979 to July 1984. The results were obtained as follows: 1) The incidence was 9.9% of epileptics who visit to our clinic at the same period of time. 2) In...
A Study on Changes of Serum Prootein, Immunoglobulins, and Electrolyte Metabolism in Childhood Nephrotic Syndrome after Steroid Therapy.
Kyung Rae Moon, Chang Soo Ra
Clin Exp Pediatr. 1986;29(1):32-44.   Published online January 31, 1986
The author determined serum and 24hr urine protein(total protein and albumin), immunoglobulins(lgG, IgA, and IgM) and serum electrolytes(Na, K, Ca, P, Mg, and Cl) in 5 cases of childhood nephrotic syndrome before and after steroid therapy, until urinary excretion of protein was negative (remission).The results observed are summarized as follows; 1) Serum protein; Before treatment, the mean serum total protein...
Case Report
Myelodysplastic syndrome Transformed into Erythroleukemia.
Sun Hee Kim, Don Hee Ahn, Keun Chan Sohn, Jung Il Suh, Jung Hee Um, Hea Ran Park
Clin Exp Pediatr. 1985;28(12):1231-1237.   Published online December 31, 1985
Myelodysplastic syndrome is a disorder of the marrow stem cell characterized initially by ineffective erythropoiesis, an abnormal bone marrow, and peripheral blood cytopjenia. Recently MDS was classified into 5 subtypes by the F rench-American-British (FAB) Cooperative Group: (1) Refractory anemia(R.A.), (2) RA with ring sideroblast, (3) RA with excess of blast(RAEB), (4) Chronic myelomonocytic leukemia (CMML) and (5) RAEB in transformation. We...
A Case of Genetic Skeletal Dysplasias.
Jeh Hoon Sin
Clin Exp Pediatr. 1985;28(11):1125-1129.   Published online November 30, 1985
Genetic skeletal dysplasias(osteochondrodysplasias) are a heterogenous group of conditions characterized by disordered growth of the various components of the skeleton, leading to disproportionate short status, deformity, or other structural and functional abnormalities of individual skeletal elements. Author experienced a case of the genetic skeletal dysplasia newborn who was born in Dong Bu City Hospital.
Two Case of Watson-Alagille Syndrome.
Heon Seok Han, Soo Heum Lim, Young Sun Kim, Jeong Kee Seo, Hyung Ro Moon
Clin Exp Pediatr. 1985;28(10):1047-1051.   Published online October 31, 1985
Watson-Alagille syndrome (Arteriohepatic dysplasia, Syndromatic paucity of interlobular bile duct), a disease characterized by chronic liver disease, characteristic facies, cardiova scular abnormalities, and vertebral arch abnormalities has paucity of interlobular bile ducts on histologic examination of liver. We experienced two cases of Watson-Alagille syndrome in a 7-month-old male infant and a 12-month-old male infant who had the chief complaint of...
A case of Congenital Nephrotic Syndrome.
Kwang Nam Kim, Kwang Hyun Kim, In Joo Seol, Ha Baik Lee, Chong Moo Park
Clin Exp Pediatr. 1985;28(9):931-935.   Published online September 30, 1985
The congenital nephrotic syndrome is characterized by large placenta, low birth weight, early clinical findings, delayed growth and development and resistance to treatment. Authors experienced a case of characteristic of congenital nephrotic syndrome in a girl, who was admitted to the Pediatric Department of HUH at 28 days of age because of generalized edema, abdominal distension with vomiting and diarrhea....
Original Article
Bone Marrow Cell Culture(GM-CFU) in Anaplastic Anemia of Children.
Jae Sun Jung, Chang Yee Hong
Clin Exp Pediatr. 1985;28(9):888-898.   Published online September 30, 1985
Bone marrow cell cultures (GM-CFU) were performed in the 15 cases of children with aplastic anemia and the correlation with the clinical course were investigated. They have been treated with androgen with or without low dose prednisone and supportive care. Bone marrow cell cultures from 8 children without any evidence of aplastic anemia were performed as a control. 1)In control...
Case Report
Three Cases of Congenital Hypoplastic Anemia.
Heui Jeong Kwon, Myung Hyun Lee, Jung Hwan Choi, Hyo Seop Ahn, Chang Yee Hong
Clin Exp Pediatr. 1985;28(8):829-835.   Published online August 31, 1985
Congenital hypoplastic anemia is a rare disease characterized by aplasia or severe hypoplasia of the erythron, with onset usually at birth or during early infancy. This report presented three cases of congenital hypoplastic anemia in 3 infants with pallor and irritability which were noticed since one to three months of age. Three cases were treatsd with prednisolone and the courses of...
A Case of Acute Lymphocytic Leukemia Successfully Treated with Allogeneic Bone Marrow Transplantaion.
In Kyung Sung, Byung Churl Lee, Kyong Su Lee, Du Bong Lee, Chong Won Park, Chun Choo Kim, Dong Jip Kim
Clin Exp Pediatr. 1985;28(8):805-811.   Published online August 31, 1985
A 8-year old boy with acute lymphocytic leukemia who had shown resistance to repeated combination chemotherapies, was successfully grafted with bone marrow from his HLA- matched sister. He was in the third partial remission at the time of bone marrow transplantation. He was conditioned with cyclophosphamide 60 mg/kg/day on two consecutive days, followed by 800 rads total body irradiation. Marrow...
A Case of Congenital Hypoplastic Anemia.
Sae Jin Lee, Moon Chung Cho, Kyung Sook Cho, Doo Sung Moon, Chong Dae Cho
Clin Exp Pediatr. 1985;28(8):801-804.   Published online August 31, 1985
We observed a case of congenital hypoplastic anemia in a 10 month old male patient who was diagnosed through bone marrow aspiration. This steroid-unresponsive patient has been maintaining a concentration of hemoglobin compatible with health from supportive transfusion therapy. A brief review of related literature was made.
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