- Case Report
- Familial Hemophagocytic Lymphohistiocytosis
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Dong Un Kim, Dae Kyun Koh, Yeon Dong Lee, Jae Kyun Hur, Kyoo Hong Cho, Suk Jin Kang
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Clin Exp Pediatr. 1994;37(9):1279-1285. Published online September 15, 1994
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Familial hemophagocytic lymphohistiocytosis (FHL) is a rare disease characterized by fever, hepatosplenomegaly, cytopenia and non-malignant lymphohistiocytic infiltration with hemophagocytosis in reticuloendothelial organs.
We experienced three cases of FHL in identical male twins and their younger brother who presented with fever and severe hepatosplenomegaly. Cytompenia, elevated serum transaminase and low serum albumin levels, hypertriglyceridemia were common laboratory findings of them. One of... |
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- A Case of Idiopathic Hypereosinophilic Syndrome
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Bin Cho, Jin Tack Kim, Joon Sung Lee, Kyoo Hong Cho
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Clin Exp Pediatr. 1994;37(7):1020-1027. Published online July 15, 1994
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The idiopathic hypereosinophilic syndrome(HES) represents a heterogenous group of disorder characterized by prolonged eosinophilia of undetectable cause and multiorgan system dysfunction.
Bone marrow is the most frequentry involved organ, but the most severe clinicopathologic involvement is heart. The major cause of death in patients with the HES is cardiac dysfunction especially congestive heart failure resulted from endocardial fibrosis and restrictive cardiomyopathy.
We... |
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- Original Article
- Clinical Observation for Prematurity and Low Birth Weight Infant.
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Kyung Nam Kim, Jong Wan Kim, Kyoo Hong Cho, Young Heon Kwak
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Clin Exp Pediatr. 1982;25(12):1197-1202. Published online December 31, 1982
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Infants who are delivered prior to the term are subject to various disorders which complicate
their neonatal course. Neonatal mortality rises progressively with increasing degrees of
prematurity.
We attempted to know the incidence of birth rate and mortality rate for prematurity and
low birth weight infants who were delivered at Our Lady of Mercy Hospital, Catholic
Medical College located in Bupyung Dong, Incheon during the... |
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