• Search
  • Advanced Search

Search

  • HOME
  • Search
Original Article
Congenital Esophageal Stenosis : with Special Reference to Diagnosis and Postoperative Complications
Ju Young Jang, Jae Seong Ko, Kwi Won Park, Woo Seon Kim, In Won Kim, Ja Jun Jang, Jeong Kee Seo,
Clin Exp Pediatr. 1999;42(4):535-544.   Published online April 15, 1999
Purpose : Congenital esophageal stenosis(CES) is one of the rare causes of recurrent vomiting during infancy and childhood. We studied the diagnostic and therapeutic tools and postoperative complications for early diagnosis and adequate management of CES. Methods : Fourteen cases of CES were evaluated for clinical manifestations, findings of esophagogram and esophagoscopy, classification of pathologic findings and postoperative complications. Results : Most...
Clinical Profiles and Anatomic Classification of Intestinal Malrotation
Jung A Kim, Jae Seong Ko, Jeong Kee Seo, Kwi Won Park, Woo Sun Kim, In One Kim
Clin Exp Pediatr. 1999;42(4):526-534.   Published online April 15, 1999
Purpose : Intestinal malrotation is a developmental anomaly and may be complicated by volvulus and intestinal necrosis. We performed anatomic classification and compared clinical profiles to understand their relationship. Methods : Twenty-eight children were diagnosed as intestinal malrotation at Seoul National University Children's Hospital between Jan. 1980 to Dec. 1995. The patients were classified into 4 groups by age at...
A Result of Treatment of Malignant Germ Cell Tumors in Childhood
Hyoung Jin Kang, Jun Ah Lee, Hyo Jeong Han, Hyoung Su Choi, Hyeon Jin Park, Ki Woong Sung, Eun Sun Yoo, Hee Young Shin, Hyo Seop Ahn, Kwi Won Park, Byung Keu Cho, Hwang Choi, Chul Woo Kim
Clin Exp Pediatr. 1997;40(12):1707-1718.   Published online December 15, 1997
Purpose : Germ cell tumors have variable clinical characteristics according to the age, sex, primary site, and pathologic diagnosis. To provide the therapeutic principle, the clinical characteristics, response to the treatment, and prognostic factors were analyzed. Methods : Medical records of 57 children who were diagnosed as malignant germ cell tumor in Seoul National University Children' s Hospital from January 1986 till June 1996 were...
Case Report
A Case of Ischemic Enteritis
Ran Lee, Jeong Kee Seo, Kwi won Park, Jong Je Kim
Clin Exp Pediatr. 1997;40(2):254-259.   Published online February 15, 1997
Ischemic enteritis is caused by embolism or thrombosis of superior mesenteric artery and nonocclusive ischemia. Mesenteric venous thrombosis, drugs, and vasculitis are less frequent etiologic factors. In children, occlusion of microcirculation by fibrin thrombi initiated by endotoxemia may be an etiology. Severe abdominal pain, vomiting, and diarrhea with evidence of gross or microscopic bleeding are common presenting symptoms. Angiography may be...
Four Cases of Congenital Esophageal Stenosis Due to Tracheobronchial Remnants
Gi Woong Sung, So Young Lee, Yeon Ho Choi, Kyoung Mo Kim, Jeong Kee Seo, In Won Kim, Kwi Won Park, Jong Je Kim
Clin Exp Pediatr. 1996;39(2):273-279.   Published online February 15, 1996
Esophageal stenosis due to tracheobronchial remnants is a rare cause of congenital esophageal stenosis. The cause is thought to be esophageal sequestration of tracheobronchial remnants during embryonic separation. Errors in diagnosis are common and high index of suspicion is required for accurate diagnosis, and resection of primary site with anastomosis is recommanded. Although a rare entity, esophageal stenosis due to...
Original Article
Infantile Choledochal Cyst Presenting with Neonatal Cholestasis; Review of Anatomical and Clinical Aspect
Jae Won Jeong, Jeong Kee Seo, Kwi Won Park, In Won Kim
Clin Exp Pediatr. 1995;38(12):1629-1637.   Published online December 15, 1995
Purpose : Extrahepatic biliary atresia, neonatal hepatitis, Allagille syndrome are most common primary causes of the neonatal cholestasis. Infantile choledochal cyst is another primary disease presenting with neonatal cholestasis but its incidence is so low that it has been reported rarely. Choledochal cyst in infancy has been known to have clinically and anatomically different characteristics from ones after infancy. Thus...
Case Report
A Case of \Intractable Ulcerating Enterocolitis\" of Infant"
Ju Young Jeong, Jeong Kee Seo, Kwi Won Park, Je Geun Chi
Clin Exp Pediatr. 1995;38(2):264-270.   Published online February 15, 1995
Intractable ulcerating enterocolitis of infancy is uncommon, inhereditary disease characterized by ulcerating stomatitis, severe perianal disease, affecting the whole gastrointestinal tract, mainly colon with flask shaped large ulcer. It was first described by Sanderson et al in 5 cases of infant with intractable diarrhea having above clinical manifestation. It should be differentiated with Crohn's disease and Behcet's disease. We experienced a...
A Case of Intestinal Lymphangiectasia
Yae Kyung Suh, Kyung Hee Park, Chul Ho Jang, Bum Soo Park, Jeong Kee Seo, Sung Hae Park, Je Geun Chi, Kyung Mo Yeon, Kwi Won Park
Clin Exp Pediatr. 1992;35(12):1737-1743.   Published online December 15, 1992
Intestinal lymphangiectasia is a primary or secondary disorder of the gastrointestinal tract, which is associated with lymphatic dysfuction and protein-losing enteropathy. It's clinical manifestations vary widely, but the main symptoms are abdominal distention, edema, abdominal pain and growth failure. We described a 15-yr-old boy, who suffered from above symptoms since third year of his age and diagnosed by duodenal endoscopy which...
Original Article
A case of Caroli's disease.
Seong Hee Jung, Cheol Ho Chang, Han Tchah, Jeong Kee Seo, Kwi Won Park, In One Kim, Kyung Mo Yeon, Je Geun Chi
Clin Exp Pediatr. 1991;34(2):261-266.   Published online February 28, 1991
Caroli’s disease was first described by Caroli in 1958 and characterized by segmental cystic dilatation of the intrahepatic bile ducts. There is stasis of bile with stone formation in the dilatated ducts, giving rise to frequent attacks of pain and cholangitis. In the past, diagnosis of the Caroli’s disease is rarely established prior to operation and subsequent cholangiography. Recently, with ultrasonography, computerized tomography, radioisotope...
A Case of Mucinous Cystadenocarcinoma in a Premenarchal Girl.
Hong Hoe Koo, Sang Oh Na, In Sang Jeon, Hyo Seop Ahn, Wan Suk Park, Suk Koo Lee, Kwi Won Park, Chong Jai Kim, Je Geun Chi
Clin Exp Pediatr. 1990;33(1):124-128.   Published online January 31, 1990
In childhood, cancer of the ovary is highly unusual. It is responsible for only 1—2% of cancers found in patients under the age of 17. The frequency with which the various histologic types of ovarian neoplasm occur in childhood differs from that in adults. Epithelial tumors account for 70% to 80% of ovarian neoplasms in adults but only 20% in patients less than...
A Clinical Observation on Esolhageal Atresia and Tracheoesophageal Fistula.
In Sang Jeon, Jung Hwan Choi, Jeong Kee Seo, Chong Ku Yun, Sung Chul Lee, Kwi Won Park, Woo ki Lee
Clin Exp Pediatr. 1988;31(6):691-699.   Published online June 30, 1988
To study the clinical characteristics of esophageal atresia and tracheoesophageal fistula, we carried out a retrospective review on medical records of 39 patients who were diagnosed as that by the operation, autopsy or radiolgy at the department of Pediatrics and Pediatric Surgery, Seoul National University Hospital between January 1980 and June 1987. The results were summarized as follows; 1) Type A was most common (94.8%) among...
Clinical Observation on Splenectomized Children.
Mi Ryung Um, Jae Won Song, Yong Yull Koh, Jeong Kee Seo, Hyo Seop Ahn, Chang Yee Hong, Kwi Won Park
Clin Exp Pediatr. 1987;30(5):511-517.   Published online May 31, 1987
A clinical study was performed on 26 cases of splenectomized children who had been seen at the Department of Pediatrics, Seoul National University Hospital, during the period of 7 years 7 months from January 1978 to July 1985. The results were as follows: 1) Primary diseases were hereditary spherocytosis (8 cases), Hodgkin disease for staging laparotomy (8 cases), ...
Case Report
Hepatoblastoma with Rupture and Hemorrhage.
Kwang Wook Ko, Hyung Ro Moon, Je Geun Chi, Kwi Won Park
Clin Exp Pediatr. 1985;28(12):1261-1261.   Published online December 31, 1985
Tracheal Foreign Body Associated with Esophageal Duplication Cyst.
Kwang Wook Ko, Je Geun Chi, Kwi Won Park
Clin Exp Pediatr. 1985;28(10):1052-1052.   Published online October 31, 1985
A Case Report of Caroli's Disease.
Hun Jong Chung, Jeong Kee Seo, Kwang Wook Ko, Kwi Won Park, Woo Ki Kim
Clin Exp Pediatr. 1985;28(7):731-736.   Published online July 31, 1985
A case of Caroli's disease was presented and review of the literature was done. The patient was a 3 year old girl and had recurrent episodes of jaundice, abdominal pain and vomiting. Dilatation of the left intrahepatic bile duct was clearly shown on the operative cholangiography.
Four Cases of Papillary Thyroid Cancer in Childhood.
Sei Weon Yang, Sei Won Park, In Sil Lee, Hyo Seup Ahn, Hyung Ro Moon, Chang Yee Hong, Kwi Won Park, Je Geun Chi
Clin Exp Pediatr. 1984;27(3):282-287.   Published online March 31, 1984
Papaillary thyroid cancer is a rare lesion in children. It progresses slowly and its prognosis is relatively good. A painless nodule in the thyroid or in the neck is the usual first evidence of disease. Cervical lymph node involvement is usually present at the time of the initial diagnosis and is often bilateral. The lungs are the most common site...
Pancreatic pseudocyst associated with severe adhesive ileus.
Kwang Wook Ko, Je Geun Chi, Kwi Won Park
Clin Exp Pediatr. 1983;26(10):1044-1047.   Published online October 31, 1983
Congenital biliary atresia.
Kwang Wook Ko, Je Geun Chi, Kwi Won Park
Clin Exp Pediatr. 1983;26(1):106-106.   Published online January 31, 1983
BCGitis.
Kwang Wook Ko, Je Keun Ji, Kwi Won Park
Clin Exp Pediatr. 1982;25(12):1295-1300.   Published online December 31, 1982
Jejunal atresia with meconium peritonitis and sepsis.
Kwang Wook Ko, Je Geun Chi, Kwi Won Park
Clin Exp Pediatr. 1982;25(9):972-976.   Published online September 30, 1982
Original Article
A Clinicostatistical Study of Congenital Alimentary Tract Obstruction.
Sang Pok Suck, Yong Soo Youn, Han Woong Choi, Woo Ki Kim, Kwi Won Park
Clin Exp Pediatr. 1981;24(1):36-44.   Published online January 15, 1981
Clinicostatistical datsa on 314 patients with congenital alimentary tract obstruction at the Department of Pediatrics and Pediatric Surgery of Seoul National University Hospital from January, 1974 to July, 1980 are presented and reviewed. The results are as follows; 1. Congenital megacolon(133 cases) is the most common congenital alimentary tract obstruction, and anorectal malformations(127 cases), congental duodenal obstruction(20 cass), esophageal atresia(12...
  • PubMed Central
  • PubMed
  • Scopus
  • Directory of Open Access Journals (DOAJ)