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Original Article
Burkitt Lymphoma in Children.
Soo Jong Hong, Dong Kyu Jin, Hee Young Shin, Hyo Seop Ahn, Chang Yee Hong, Je G Chi
Clin Exp Pediatr. 1988;31(4):482-491.   Published online April 30, 1988
Seventeen cases of Burkitt lymphoma under 15 years of age who were admitted to Dept, of Ped., Seoul National University Hospital from Jan. 1979 to Dec. 1986 were reviewed and analysed. One hundred and six cases of non-Hodgkin lymphoma were seen during the same period. 1) Burkitt lymphoma accounted for 16% of non-Hodgkin lymphoma. 2) The age ranged from 10/12 year to 15 5/12 years, with...
A Case of Potter Syndrome with Bilateral Polycystic Kidneys.
Chun Hwa Lee, Jung Hwan Choi, Yong Choi, Chong Ku Yun, Yeon Lim Suh, Je G Chi, Son Moon Shin
Clin Exp Pediatr. 1987;30(11):1282-1286.   Published online November 30, 1987
In 1946, Potter described a series of 20 cases of infants in whom bilateral absence of the kidneys was associated with hypoplasia of the lungs and characteristic faces. Afterwards it has been known that any condition that causes significant reduction in urine formation or excretion will result in oligohydramnios accounts for many of the nonrenal features of Potter syndorme. We report a case...
Current Status of Congenital Malformation Statistics in Korea.
Je G Chi
Clin Exp Pediatr. 1987;30(6):595-601.   Published online June 30, 1987
Cardiac Malposition.
Sejung Sohn, Jung Yun Choi, Yong Soo Yun, Chang Yee Hong, Je G Chi
Clin Exp Pediatr. 1986;29(2):186-202.   Published online February 28, 1986
Cardiac malposition refers to any position of the heart other than a left-sided heart in a situs solitus individual. Authors analyzed the clinical, radiological, operative and autopsy findings of 69 patients with cardiac malpositions by segmental approach to describe the internal cardiac anatomy and their arterial connections. 1) Male to female sex ratio was 1.23 : 1 and 68% of cases were under...
Case Report
A Case of Acardius Twin.
Kyung Hyo Kim, Jung Soo Park, Mina Lee, Hye Kyung Lee, Sung Sik Shin, Je G Chi
Clin Exp Pediatr. 1984;27(1):84-88.   Published online January 31, 1984
A case of acardiac twins to a 30 year-old primiparous mother is presented. This case was diagnosed to have this anomaly by ultrasonography at 28 weeks and 33 weeks of gestation. The acardiac monster was delivered as the second twin without any signs of Life. It weighed 2,175 gms and was connected to the placenta by an umbilical cord having...
Original Article
Clinicao-Pathologic Study on Hyaline Membrane Disease.
Jung Woo Suk, Je G Chi
Clin Exp Pediatr. 1983;26(6):534-544.   Published online June 30, 1983
A total of 27 cases of hyaline membrane disease (idiopathic respiratory distress syndrome was studied clinically, and postmortem findings were reviewed on 14 cases that were available：for autopsy. These 27 cases were obtained during a period of 19 years from January, 1961 to December,1979, at National Medical Center, Seoul. Following results were obtained. 1. The overall incidence of hyaline membrane disease (HMD) among...
Case Report
Disseminated Intravascular Coagulation in an Infant Born after Abruptio Placentae.
Soon Ung Kang, Jung Hwan Choi, E Boong Kwon, Chong Ku Yun, Kwang Wook Ko, Je G Chi, Chul Woo Kim
Clin Exp Pediatr. 1982;25(7):730-736.   Published online July 31, 1982
Premature separation of the placenta(abruptio placentae), as a serious obstetric complication, has been recognized to be associated with disseminated intravascular coagulation(DIC) in the newborn period. However, pathologic evidence for DIC generally has been lacking or rarely reported. Recently we have experienced one case of DIC in an infant born after abruptio placentae. The infant had suffered from cyanosis, dyspnea and...
Original Article
Histiocytic Medullary Reticulosis in Children: Report of Four Cases and Analysis of Previously Reported Cases.
Eue Cho Yang, Jae Ho Lee, Soon Ung Kang, Hyo Seop Ahn, Chang Yee Hong, Je G Chi, Yong Il Kim
Clin Exp Pediatr. 1981;24(10):928-941.   Published online October 15, 1981
Histiocytic Medullary Reticulosis(H.M.R.) is a rapidly progressing fatal disease seen most often in adults, but it has been reported in children younger than 15 years of age. H.M.R. is clinically characterized by fever, wasting generalized lymphadenopathy and hepatosplenomegaly. In the terminal stage, jaundice, purpura, anemia and pancytopenia are all present with or without skin involvement. Cardinal pathologic features are systemized...
Case Report
Hyaline Membrane Disease (Five cases report including two autopsy cases).
Jun Hee Kang, Young Min Ahn, Joong Gon Kim, Chun Haeng Park, Jeong Kee Seo, Ok Ja Hwang, Chong Ku Yun, Yoon Seong Lee, Shin Eun Choi, Je G Chi
Clin Exp Pediatr. 1981;24(9):882-890.   Published online September 15, 1981
The hyaline membrane disease is not a common disease in Korea. Only a few reports of small scale are avaiable in the literature. We have experienced 5 cases of HMD during approximately 1 year period. The diagnosis was made either on characteristic clinical and roentgenological features or postmortem examination. The birth weights of these cases were in the range of...
An Autopsy Case of Agyria.
Young Ill Park, Joon Hee Oh, Tae Sub Shim, Je G Chi
Clin Exp Pediatr. 1979;22(9):799-802.   Published online September 15, 1979
An autopsy case of agyria in a newborn infant was reported. This neonate had her birth weight of 1.62kg after 40 weeks of gestation. The head circumference was 24cm(less than 3 percentile), and was slightly asymmetric. The brain weighed 60 grams. Fronto-occipital diameter was 7cm. And biparietal diameter was 6.5cm. Two small hemispheres were covered with opague congested leptomeninges, and...
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