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Case Report
One Case of Neonatal Acute Lymphocytic Leukemia.
Une Hee Choi, Sang Ki Whang, In Soon Lee, In Bok Lee, Eun Cho Yang, Heum Rea Park
Clin Exp Pediatr. 1984;27(11):1103-1107.   Published online November 30, 1984
A 26 days old male with petechiae, ecchymoses and hepatosplenomegaly was admitted to the Department of Pediatrics, at In Cheon Gil Hospital on Jnue, 1983. Peripheral blood smear and bone marrow studies revealed acute lymphocytic leukemia. Autopsy findings revealed that abundant lymphoblastic leukemic cell infiltrated in bone marrow, liver, spleen, kidney and other organs in male newborn infant who died 29 days after birth. And...
A Case of Congenital Cystic Adenomatoid Malformation of Lung Associated with Fetal Ascites.
In Soon Lee, Un Hee Choi, Woon Sik Kim, Heum Rea Park
Clin Exp Pediatr. 1983;26(7):722-725.   Published online July 31, 1983
Cystic adenomatoid malformation is a specific form of cystic lung disease characterized by a cuboidal and columnar epithelium. Reported cases had anasarca or polyhydramnios. We have experienced a case of cystic adenomatoid malformation of lung associated with. fetal ascites and reviewed the pertinent literatures briefly.
A Case Report of Congenital Multiple Jejunoileal Atresia with Massive Mesenteric Defect.
Ji Young Kang, In Soon Lee, Sang Kyo Lee, Byung Wha Lee
Clin Exp Pediatr. 1983;26(3):271-274.   Published online March 31, 1983
This is a case report of congenital multiple jejunoileal atresia with massive mesenteric： defect around the ileum. He was born by mid-wife and transferred to our Dep't of Pediatrics，. In Cheon Gil Hospital on Feb. 9th’ 1981. Vomiting noted one time 17 hours after birth and abdominal film disclosed markedly geseous distention of stomach and duodenum and no gas。 in the ileum and colon....
A Case of 18p- Syndrome with Congenital Hypothyroidism.
Ji Young Kang, In Soon Lee, Woon Sik Kim
Clin Exp Pediatr. 1983;26(1):102-105.   Published online January 31, 1983
We have experienced a case of 18p- syndrome with congenital hypothyroidism in a 16-month-old girl who had microcephaly, flat nasal bridge, failure to thrive, left inguinal hernia and umbilical hernia. The diagnosis was confirmed by physical findings, cytogenetic study, thyroid function test and thyroid scanning. The review of the related literature was made briefly.
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