- Original Article
- A Case of Agnogenic Myeloid Metaplasia.
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Min Sook Um, Jo Sam koo, Jae Sun Park, Sook Ja Park, Hae Kyung Jang
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Clin Exp Pediatr. 1988;31(11):1486-1493. Published online November 30, 1988
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Agnogenic myeloid metaplasia characterized by marrow fibrosis, leukoerythroblastic anemia,
extramedullary hematopoiesis with varying degree of hepatosplenomgaly, is very rare disorder in
children.
We experienced a case of agnogenic myeloid metaplasia 34 months old male patient who was
presented with pallor, generalized petechiae, marked hepatosplenomegaly and intermittent fever.
Peripheral blood smear showed leukoerythroblastosis, poikilocytosis and tear drop cells. Bone
marrow aspiration and biopsy showed fibrosis with no... |
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- A Clinical Study of Type A Hepatitis Confirmed by IgM Anti-HAV.
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Oh Kyung Lee, Sung Seek Lee, Keun Chul Choi, Myung Ho Lee, Sook Ja Park
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Clin Exp Pediatr. 1984;27(8):778-785. Published online August 31, 1984
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79 children with Type A Hepatitis who were admitted to the pediatric department of the Presbyterian Medical Center from April 1, 1983 to October 31, 1983 were clinically analized and we report the following result. 1) Type A Hepatitis occupied 8% of total in patients and 88% of total Hepatitis patients. 2)The peak age incidence was between 7 and 9 years... |
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- Case Report
- Two Cases of Di Guglielmo Syndrome.
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Seok Ku Kim, Seong Ja Jeon, Chul Lee, Myung Ho Lee, Sook Ja Park
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Clin Exp Pediatr. 1983;26(3):289-284. Published online March 31, 1983
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Di Guglielmo Syndrome is a relatively rare disease in childhood and refers to an acute or
chronic myeloproliferative disorder in which erythrocytes and their precursors are the cells
predominantly involved in the leukemic process. We experienced two cases of Di Guglielmo syndrome,
an llyear-old girl and a 14 year-old boy, who had the chief complaints of severe anemia, fever,
dizziness and general... |
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- A Case of Histiocytic Medullary Reticulosis in 17 Month-old Child.
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Oh Kyung Lee, Wan Seob Kim, Myung Ho Lee, Sung Seek Lee, Sook Ja Park
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Clin Exp Pediatr. 1983;26(12):1220-1225. Published online December 31, 1983
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Histiocytic medullary reticulosis(HMR) is a rare, uniformly fatal, acute disease of the
reticuloen dothelial system. Major features are fever, malaise, weakness, weight loss,
lymphadenopathy, hepatosplenomegaly, jaundice and purpura. Common laboratory finding is severe pancytopenia. Cardinal pathologic feature is proliferation of atypical, neoplastic, erythrophagocytic
histiocytes. Recently we experienced a case of HMR in 17 month-old male child. The clinical findings
and... |
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- A case of myelofibrosis.
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Hae Jung Cho, Keun Chull Choi, Chul Lee, Myong Ho Lee, Sook Ja Park
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Clin Exp Pediatr. 1982;25(9):945-953. Published online September 30, 1982
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The so called “Myelofibrosis” within the category of myeloproliferative disorders consists
of various degrees of leukoerythroblatosis, bone marrow fibrosis, and extramedullary hema-
topoiesis with hepatosplenomegaly.
Primary myelofibrosis occurs predominantly in adults and few in childhood. We experie-
nced one case of myelofibrosis, at 17 month old male patient.
He was admitted due to intermittent fever, pallor and abdominal distension. On admission,
hepatosplenomegaly, anemia and generalized petechia... |
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- Original Article
- Study on cord blood hemoglobin and etiology of neonatal anemia.
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Chul Lee, Hae Jung Cho, Myung Ho Lee, Sook Ja Park, Young Hae Lee
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Clin Exp Pediatr. 1982;25(9):906-913. Published online September 30, 1982
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Capillary samples obtained by skin prick, generally from the heel or toe, have a higher
hemoglobin Concentration than simultaneously collected venous samples. So, capillary values
should not be compared to previously obtained cord venous blood values when one is looking
for changes in hemoglobin, concentration during the first week of life. Cord venous blood
hemoglobin and hemotocrit of 309 normal newborn infants have been... |
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