• Search
  • Advanced Search

Search

  • HOME
  • Search
Original Article
A Clinical Observation on Fulminant Hepatitis in Children.
Hoan Jong Lee, Jeong Kee Seo, Hyung Ro Moon
Clin Exp Pediatr. 1987;30(4):406-415.   Published online April 30, 1987
Twenty-seven cases of fulminant hepatitis in children were retrospectively analyzed. The overall survival rate was 11%. The interval between onset of encephalopathy and death, and that between jaundice and death were 2-26 days (median 4 days), 4-61 days (median 14 days), respectively. HBs antigenemia was detected in 24%, HAV IgM was negative in 5 patients tested, and 4 cases were suspected as non-A, non-B...
A Clinical and Pathologic Study on Chronic Hepatitis in Infancy and Childhood.
Ki Sub Jung, Chan Ill Park
Clin Exp Pediatr. 1987;30(1):35-44.   Published online January 31, 1987
A clinical and pathologic study was undertaken on 46 cases of chronic hepatitis who had been admitted to Department of Pediatrics, Yonsei University College of Medicine during the period of 6 years from August, 1979 to July, 1985. The results were as follows: 1) Of 46 patients with chronic hepatitis, 40 cases were caused by hepatitis B virus, 3 cases by autoimmunity, and in 3 cases...
Case Report
A Case of Aplastic Anemia Following Hepatitis.
Woo Yeong Chung, Seung Won Park, In Soon Park, Chul Ho Kim, Soo Yong Lee
Clin Exp Pediatr. 1983;26(8):812-815.   Published online August 31, 1983
We experienced a case of aplastic anemia following hepatitis in a 11-year old male child. He was admitted because of pallor and gum bleedings with an episode of hepatitis 2 months prior to this admission. On admission CBC showed pancytopenia and there was marked hypocellularity of all hematopoietic elements in bone marrow aspiration. Transfusion and treatment with prednisolone and oxymetholone were tried but...
A Case Of Choledochal Cyst In A Neonate.
Jong Man Lee, In Kyung Sung, Jong Seung Kim, Chang Kyu Oh
Clin Exp Pediatr. 1982;25(10):1068-1072.   Published online October 31, 1982
Congenital choledochal cyst is a rare disease, especially in fetal life and early infancy age. Our case was a 66 days old female baby who had the symptoms of jaundice, clay-colored stool, intermittent vomiting since birth and abdominal distension. Final diagnosis was choledochal cyst with neonatal hepatitis. An early accurate preoperative diagnosis has been associated with a marked decrease in the mortality. Roux-en-Y choledochocystojejunostomy was done. We...
TOPICS

Browse all articles >

ARTICLE CATEGORY

Browse all articles >

BROWSE ARTICLES
FOR CONTRIBUTORS
ABOUT
Editorial Office
Korean Pediatric Society
#1606 Seocho World Officetel, 19 Seoun-ro, Seocho-ku, Seoul 06732, Korea
Tel: +82-2-3473-7306    Fax: +82-2-3473-7307    E-mail: office@e-cep.org                

Clinical and Experimental Pediatrics is an open access journal. All articles are distributed under the terms of the Creative Commons Attribution NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/)

Copyright © 2025 by Korean Pediatric Society.      Developed in M2PI