- Original Article
- Serum Albumin Concentrations and Clinical Disorders by Gestational Ages in Preterm Babies
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Mia Lee, Soo Youn, Baek Keun Lim, Jong Soo Kim
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Clin Exp Pediatr. 2005;48(2):148-153. Published online February 15, 2005
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Purpose : The aim of this study was to determine the reference ranges of serum albumin levels depending on the gestational ages of preterm infants. We also intended to compare the mean serum albumin levels between groups of preterm infants that did not develop clinical disorders later, and groups that did develop clinical disorders such as respiratory distress syndrome, intraventricular... |
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- Case Report
- A Case of Vascular Leak Syndrome During Induction Chemotherapy of Acute Lymphoblastic Leukemia(T Cell Type)
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Kye Wool Kang, Hwang Min Kim, Won Kyu Choi, Baek Keun Lim, Chang Hun Lee
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Clin Exp Pediatr. 2001;44(9):1041-1046. Published online September 15, 2001
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Vascular leak syndrome(VLS) is characterized by endothelial damage, which causes extravasation
of plasma proteins and fluid from capillaries into the extravascular space. It has been suggested
that the increased vascular permeability is the result of an IL-2-induced suppression of endothelin-
1 secretion by endothelial cells, an IL-2-induced activation of the complement cascade or
TNF-αrelease from IL-2-activated T-cells. A 13-year-old male patient visited our hospital... |
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- Original Article
- Mean Corpuscular Hemoglobin Concentration as a Discriminating Tool between Hereditary Spherocytosis and Intravascular Hemolysis
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Hae Young Park, Hwang Min Kim, Kyoung Ah Lee, Dong Il Won, Sei Myeng Park, Seok Won Park, Baek Keun Lim, Kil Young Kim
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Clin Exp Pediatr. 2001;44(6):664-668. Published online June 15, 2001
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Purpose : The purposes of this study were to elucidate the diagnostic significance of mean corpuscular hemoglobin concentration(MCHC) for various kinds of hemolytic anemia, the mechanism of elevated MCHC in hereditary spherocytosis(HS).
Methods : The subjects consisted of 39 cases of HS(group 1), 31 cases of intravascular hemolysis (IH) such as DIC, snake bite or hemolytic uremic syndrome(group 3), and sex... |
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- Case Report
- A Case of Propionic Acidemia
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Woo Seop Yeoum, Kwang Wook Lee, Byeong Ho Chae, Baek Keun Lim, Hong Jin Lee
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Clin Exp Pediatr. 1999;42(8):1159-1164. Published online August 15, 1999
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Propionic acidemia is an autosomal-recessive inborn error of branched-chain amino acid metabolism. It is caused by deficient activity of propionyl-coenzyme A carboxylase and is characterized by a spectrum of clinical and biochemical findings. It usually manifests in the neonatal period or early infancy. Since Childs et al first described the propionic acidemia of infants in 1961, it has rarely been... |
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- A Case of Idiopathic Hypoparathyroidism Associated with Graves' Disease
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Eun Young Jang, Hwang Min Kim, Baek Keun Lim, Jong Soo Kim
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Clin Exp Pediatr. 1999;42(5):716-721. Published online May 15, 1999
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Graves' disease is a relatively rare endocrinologic disorder in childhood age and often associated with other endocrinologic disorders such as type I diabetes mellitus and Addison's disease etc. Also, it is associtated with non-endocrinologic autoimmune diseases such as systemic lupus erythematosus, myasthenia gravis, idiopathic thrombocytopenic purpura, vitiligo and pernicious anemia. However, idiopathic hypoparathyroidism associated with Graves' disease is very... |
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- Original Article
- Diagnostic Value of Reticulated Platelet in Thrombocytopenia
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Song Hee Park, Hwang Min Kim, Baek Keun Lim, Young Hak Shim, Chang Hoon Lee, Myung Seo Kang
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Clin Exp Pediatr. 1997;40(6):850-856. Published online June 15, 1997
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Purpose : We performed this study to determine the diagnostic significance and useful
cut-off value of reticulated platelet, which can be used for discriminating the destructive
thrombocytopenia from underproductive thrombocytopenia.
Methods : We evaluated 37 patients with thrombocytopenia who were admitted to the
Wonju christian hospital from March to July, 1995. All patients were evaluated with bone
marrow megakaryocyte count. We divided them into two... |
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- Case Report
- A Case of Multicystic Encephalomalacia in a Liveborn Twin with a Stillborn Co-twin
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Mi Ya Park, Kyung Hee Kim, Jae Seung Yang, Baek Keun Lim, Jong Soo Kim
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Clin Exp Pediatr. 1997;40(3):429-433. Published online March 15, 1997
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Multicystic encephalomalacia is the condition defined anatomically by the presence of
multiple cavities in the great part of both cerebral hemispheres. The most common
cause of the condition was regarded as the circulatory disturbance during the perinatal period. Also,neonatal asphyxia was the most important cause of the circulatory disturbance.
But we experienced a case of multicystic encephalomalacia in a liveborn twin with a
stillborn... |
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- A Case of Acyclovir Induced Acute Tubular Necrosis
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Mi Ya Park, Mee Kyung Namgoong, Hwang Min Kim, Baek Keun Lim, Sun Hee Jung
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Clin Exp Pediatr. 1995;38(9):1283-1287. Published online September 15, 1995
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Acyclovir is generally regarded as a safe and highly effective antiviral agent in normal, as well as in immunocompromised hosts. Major renal complication was unusual. However, reversible renal dysfunction has been reported. The impairment of renal nephropathy resulting from crystal formation in the renal tubules or the collecting ducts.
But we experienced a case of immunocompetent patient who developed severe... |
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- Three Cases of Pneumoperitoneum in Ventilated Newborns
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Chun Ok Yang, Ho Young Lee, Won Kju Choe, Baek Keun Lim, Jong Soo Kim
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Clin Exp Pediatr. 1995;38(7):1006-1011. Published online July 15, 1995
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Pneumoperitoneum in the newborn is usually a surgical emergency resulting from gastroint-estinal perforation. However, pneumoperitoneum can occur secondary to a pulmonary air leak which progresses from the mediastinum to the retroperitoneum by way of perivascular spaces and then to the peritoneum following rupture. We have observed this phenomenon in three ventilated newborn. A brief review of the related literatures was... |
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- A Case of Congenital Dyserythropoietic anemia Type IV
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Hwa Young Jeon, Hwang Min Kim, Baek Keun Lim, Duk Woo Park, Myung Seo Kang, Young Kun Deung
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Clin Exp Pediatr. 1995;38(5):702-706. Published online May 15, 1995
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Congenital dyserythropoietic anemia(CDA) is characterized by ineffective erythropoiesis an d increased numbers of multinucleated red cell precursors in the marrow. This syndrome has b een subdassified on the basis of morphologic and serologic differences in the red cell pecursors. There are some patients with congenital dyserythropoietic anemia who do not fit into the conventional classification of type I, II, or... |
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- Original Article
- Relationship of Echocardiographic, Shunt Flow, and Angiographic Size
to the Operation Diameter of the Atrial Septal Defect
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Dae Kwon Hong, Hae Yong Lee, Baek Keun Lim
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Clin Exp Pediatr. 1995;38(2):232-239. Published online February 15, 1995
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This report is based on analysis of admissions to the department of pediatric at the Wonju Christian Hospital during the 3 3/4-year period from January 1989 to September 1993 with an Isolated ostium secundum ASD.
Several methods of assessment of ASD size, namely, echographic, pulmonary-to-systemic flow ratio(Qp:Qs), and angiographic measures, were undertaken in a group of 37 patients, who were being... |
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- Case Report
- A case of Central Diabetes Insipidus Associated with Brachycephaly
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Woo Sik Kang, Mee Kyung Namgoong, Jae Seung Yang, Baek Keun Lim, Jong Soo Kim
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Clin Exp Pediatr. 1994;37(2):282-287. Published online February 15, 1994
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Brachyecphaly is a kind of craniosynostosis. Because of premature closure of the coronal suture, the skull is shorter in the anteroposterior diameter but is widened with a high vault and the occiput and borehead are flattened. Diabetes insipidus had been reported in oxycephaly.
We have experienced a case of central diabetes insipidus associated with brachcephaly. A brief review of related literatures... |
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- Original Article
- Analysis on the Cause of Eosinophilia in Premature Infants
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Woo Sik Kang, Suck Kyu Hur, Mee Kyung Namgoong, Hwang Min Kim, Baek Keun Lim
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Clin Exp Pediatr. 1994;37(1):47-53. Published online January 15, 1994
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Eosinophilia is a common finding in premature babies during the neonatal period. Serial eosinophil counts were determined in 94 hospitalized, appropriately grown premature infants whose gestational ages ranged from 28 to 36 weeks. The incidence, sseverity and etiologic factors of eosinophila were retrospectively studied in premature infants, who were divided into three groups according to their gestational age.
The results were... |
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- Clinical Observation of Aseptic Meningitis Associated with Mucocutaneous Lymph Node Syndrome
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Jae Hee Han, Seon Jin Ji, Mee Kyung Namgoong, Hae Yong Lee, Jae Seung Yang, Baek Keun Lim
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Clin Exp Pediatr. 1993;36(6):805-809. Published online June 15, 1993
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Clinical observation was carried out for 147 patients with mucocutaneous lymph node syndrome(MCLS) who were admitted to the Department of Pediatrics, Wonju Cristian Hospital during the period from June, 1983 to June, 1992. A spinal tap was performed on 114 of these patients and the following results were obtained.
1) The incidence of aspetic meningitis in patients with MCLS was 52.6%.(60... |
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- Case Report
- Three Cases of Purpura Fulminans
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Sun Hee Suh, Hwang Min Kim, Jae Seung Yang, Baek Keun Lim
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Clin Exp Pediatr. 1993;36(5):725-732. Published online May 15, 1993
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Purpura fulminans is one of rare consumptive coagulopathy in children. The most common prediasposing conditions of purpura fulminans are infectious disease like streptococcal infection and chickenpox. This disease is characterized by ecchymotic lesions that are usually distributed symmetrically on the lower extremities and buttocks. These ecchymotic lesions undergo necrosis, unless there is effective treatment.
We experienced 3 cases of purpura fulminans... |
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- Original Article
- Clinical Characteristics of Inborn and Outborn Infants Admitted to the NICU
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Hyun Cheol Lee, Jin Young Choi, Hwang Min Kim, Baek Keun Lim, Jong Soo Kim
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Clin Exp Pediatr. 1993;36(12):1647-1655. Published online December 15, 1993
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Regionalization of high-risk perinatal care has been advocated because intensive care of small and ill newborn infants lowers mortality and morbidity. This report is based on analysis of admissions to the Neonatal Intensive Care Unit (NICU) at the Wonju Christian Hospital during the 4-year period from January, 1988 to December, 1991. There were 786 inborn infants and 1155 outborn... |
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- Case Report
- A Case of Poststeroid Panniculitis
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Moon Sang Park, Mee Kyung Nam, Hae Yong Lee, Baek Keun Lim, Jong Soo Kim, Sun Won Hong
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Clin Exp Pediatr. 1992;35(3):406-410. Published online March 15, 1992
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Poststeroid panniculitis occuring after steroid treatment is an extremely rare entity. Multiple subcutaneous, firm, pruritic, tender nodules occur chiefly over the cheeks, arms, and trunk in young children following sudden discontinuation of large dose of steroids.
We experiened a case of poststeroid panniculitis in a 2day-old female infant with complaints of multiple subcutaneous nodules on cheeks and neck... |
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- Original Article
- The Significance of Nucleated Red Blood Cell Counts in Various Conditions Associated with Acute or Chronic Perinatal Asphyxia
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Suck Kyu Hur, Moon Sang Park, Mee Kyung Namgoong, Hwang Min Kim, Jae Seung Yang, Baek Keun Lim, Jong Soo Kim, Myung Seo Kang
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Clin Exp Pediatr. 1992;35(11):1514-1519. Published online November 15, 1992
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This study was conducted to find out the significance of nucleated red blood cell (NRBC) in neonates, especially associated with acute or chronic perinatal asphyxia. So, we compared NRBC counts in various neonatal groups, such as normal newborn, small for gestational age (SGA), premature, acute perinatal asphyxia, & hyaline membrane disease (HMD). In the first day of life, we examined... |
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- The Comparision of Brain Computed Tomography and Isotope Cisternography in Communicating Hydrocephalus
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Jong Chan Kim, Hwang Min Kim, Jae Seung Yang, Baek Keun Lim, Chul Hu, Soon Ki Hong, Young Hyuk Lee
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Clin Exp Pediatr. 1992;35(1):9-16. Published online January 15, 1992
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Brain computed tomograpy is particularly accurate in defining cerebrospinal fluid (CSF) space because of the relatively great density difference between CSF and brain parenchyma. This noninvasive procedure has very quickly become definitive in the diagnosis of hydrocephalus. However, while the typical clinical and radiological picture of a hydrocephalic patient leaves no doubt as to the need for adequate surgical treatment.... |
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- A case of myelofibrosis with juvenile xanthogranuloma.
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Jong Chan Kim, Hae Yong Lee, Hwang Min Kim, Baek Keun Lim, Jong Soo Kim, Young Hyuk Lee
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Clin Exp Pediatr. 1991;34(6):869-876. Published online June 30, 1991
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Myelofibrrosis is characterized by anemia, leukoerythroblastosis, extramedullary hematopoiesis,
hepatosplenomegaly, osteosclerosis and fibrosis of bone marrow. Idiopathc myelofibrosis is usually a
disease of the adult and is rare in the pediatric age group. Juvenile xanthogranuloma is characterized
by multiple papules on forehead and scalp. Lipid laden histiocytes and Touton giant cell are found in
skin biopsy. We experienced a case of myelofibrosis with juvenile xanthogranuloma.... |
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- Two cases of ectopic sublingual thyroid with hypothyroidism to be appeared in fetal life.
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Dong Sik Kim, Mee Kyung Namgoong, Hae Yong Lee, Hwang Min Kim, Baek Keun Lim
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Clin Exp Pediatr. 1991;34(3):426-434. Published online March 31, 1991
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Infants & children with hypothyrodism usually manifest variable skeletal abnormality. These
features are the delay in longitudinal bone growth, the delay in epiphyseal maturation (=delay in
bone age), the disturbances in bone mineralization and charateristic multiple stippled epiphysis
(cretenoid epiphyseal dysgenesis). But many pediatrician have only concerned about the delay in
epiphyseal maturation.
Epiphyseal dysgenesis can be used a marker to find out the begining... |
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- A case of citrobacter freundii osteomyelitis.
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Hyung Goo Cho, Dong Sig Kim, Hwang Min Kim, Jae Seung Yang, Baek Keun Lim, Jong Soo Kim
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Clin Exp Pediatr. 1991;34(3):408-412. Published online March 31, 1991
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Citrobacter although once regarded as nonpathogenic, has been responsible for many well-
documented pathologic conditions, especially in compromised hosts.
These include urinary tract, pulmonary and bone infections, gastroenteritis, gangrenous ulcer with
septicemia, meningitis, and brain abscess.
Citrobacter organisms have a mosaic of 0, K and H antigens that are found in the Enterobacter-
iaceae. Cross reactions with antisera of other members of the Enterobacteriaceae suggest... |
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- The normal values of platelet count, mean platelet volume and platelet distribution width in the normal newborn, small for gestational age and premature neonates.
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Eun Kyung Oh, Hae Yong Lee, Hwang Min Kim, Jae Seung Yang, Baek Keun Lim, Jong Soo Kim
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Clin Exp Pediatr. 1991;34(3):340-347. Published online March 31, 1991
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The importance of establishing authentic normal platelet count, mean platelet volume and platelet
distribution width in the newborn has been emphasized, but they have not been firmly established. We
have presented values for platelet count, mean platelet volume and platelet distribution width in the
venous blood of term, small for gestational age and premature neonates at postnatal day 1 and 7.
The results were... |
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- A Case of Esophageal Duplication.
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Hyung Kuk Ham, Jeong Kyu Seoh, Jae Seung Yang, Baek Keun Lim, Jong Soo Kim, Hee Jae Joo
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Clin Exp Pediatr. 1990;33(8):1134-1139. Published online August 31, 1990
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Esophageal duplication, a term used synonymously with enteric cyst, foregut cyst, gastroenteric
cyst, enteric duplication, and etc, is a rare developmental anomaly which occures during differentia-
tion of the larynx, trachea, and bronchi from the primitive foregut. They may cause dysphagia,
regurgitation, pneumonia, hemoptysis, and occasionally produce alarming airway obstruction.
We experienced a case with chief complaints of pale appearance and swallowing difficulty in... |
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- Three Cases of Transverse Myelopathy.
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Hae Joung Joung, Hwang Min Kim, Jae Seung Yang, Baek Keun Lim, Jong Soo Kim
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Clin Exp Pediatr. 1990;33(10):1418-1422. Published online October 31, 1990
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Transverse myelopathy is characterized by a sudden onset of motor weakness and sensory loss on
the distribution under the affected spinal cord level. And slso, autonomic nerve functions may be
disturbed at the same time.
The etiology is still unknown. But it is thought that numerous conditions and diseases are associat-
ed with it.
We experienced 3 cases of transverse myelopathy preceded by Korean hemorrhagic... |
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- A Case of Hypertrophic Cardiomyopathy in Identical Twin.
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Wea Kyoung Shin, Hae Young Lee, Hwang Min Kim, Jae Seung Yang, Baek Keun Lim, Jone Soo Kim
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Clin Exp Pediatr. 1990;33(10):1399-1405. Published online October 31, 1990
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Hypertrophic cardiomyopathy is a common genetically transmitted disorder characterized by
asymmetric septal hypertrophy and systolic anterior motion of the mitral valve.
We have recently experienced identical twin with the hypertrophic cardiomyopathy confirmed by
M-mode and 2-D echocardiography. It is the first report of hypertrophic cardiomyopathy in identical
twin in Korea. So presented this case with a review of referential literatures. |
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- Two cases of Glanzmann's thrombasthenia in brother.
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Won Mo Yang, Hyung Kook Ham, Mee Kyung Namgoong, Baek Keun Lim, Hong Sup Yoon, Kab Joon Yoon
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Clin Exp Pediatr. 1989;32(11):1574-1580. Published online November 30, 1989
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Glanzmann’s thrombasthenia is rare congenital bleeding disorder of autosomal recessive trait.
We experienced two cases of Glanzmann’s thrombasthenia in brother. The mother and elder
brother had no history of bleeding tendency. But 10 year-old and 7 year-old younger brothers had
frequent epistaxis, gum bleeding and easy bruisability.
On platelet aggregation test, mother and elder brother appeared normal responses, but the younger
brothers appeared no responses... |
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- A Case of Massive Thymic Hyperplasia.
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Hye Kyung Bae, Jung Kyu Suh, Jae Seung Yang, Baek Keun Lim, Yeun Kee Kim, Chan Il Park
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Clin Exp Pediatr. 1988;31(11):1516-1521. Published online November 30, 1988
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We have experienced a case of massive thymic hyperplasia in 2 months old female with about 1
month’s history of upper respiratory tract infection and inspiratory stridor.
The chest X-ray and chest CAT scan examination revealed superior mediastinal huge mass and so
surgical resection and pathologic examination were perfermed because of clinical suspicion of
pathologic mass. The pathologic finding of mass showed massive thymic... |
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- A Case of Dapsone Syndrome.
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Jeong Kyu Seoh, Hye Kyong Bae, Jae Seung Yang, Eung Deok Choi, Baek Keun Lim, Jong Soo Kim
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Clin Exp Pediatr. 1988;31(10):1376-1380. Published online October 31, 1988
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Dapsone syndrome is a rare hypersensitivity reaction to Dapsone. The reaction included fever,
malaise, dermatitis jaundice with hepatic dysfunction, lymphadenopathy, and hemolytic anemia.
We have experienced a case of Dapsone syndrome in a 10 years old male. This patients had taken
D.D.S. with 50 mg per day for 1 month to treat an unknown skin disease. After then, above mentioned
symptoms and signs were... |
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- Diagnosis of Meconium Aspiration by Spectrophotometric Analysis of Urine.
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Chang Yul Kim, Hye Kyung Bae, Mee Kyung Namgoong, Baek Keun Lim, Joong Soo Kim
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Clin Exp Pediatr. 1988;31(10):1275-1280. Published online October 31, 1988
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We measured optical density of aqueous extracts of meconium and meconium stained amniotic
fluid at 390 nm, 405 nm, 420 nm, 435 nm, 450 nm by spectrophotometry.
We also applied the spectrophotometric method to the urine from 25 infants with clinical sign of
meconium aspiration and from normal infants.
The absorption band at 450 nm observed on the spectra of urine was estimated as... |
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- Non-Hemolytic Hereditary Ellitocytosis born of Asymptomatic Carrier state of Hereditary Elliticytosis.
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Hae Joon Park, In Soon Ahn, Baek Keun Lim, Young Uh, Kyung Won Lee
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Clin Exp Pediatr. 1988;31(1):113-118. Published online January 31, 1988
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Hereditary elliptocytosis is characterized by elliptically shaped erythrocytes in peripheral blood
and known to be transmitted as an autosomal dominant trait, but in some cases, inherited recessively.
The clinical and hematologic expressions are variable range from healthy person with normal red cell
morphology to severe hemolytic anemia.
Recently, the authors experienced all three offsprings shown non-hemolytic hereditary el-
liptocytosis, whose parents were healthy persons with... |
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- Continuous Intravenous Glucose Infusion and Serum Glucose in Neonates.
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Hae June Park, Jung sik Rhim, Baek Keun Lim, Jong Soo Kim
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Clin Exp Pediatr. 1987;30(5):499-503. Published online May 31, 1987
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Serum glucose changes by constant infusion of glucose at the rate of 8 mg/kg/min were studied in
20 neonates. Serum glucose level elevated from 41 ±8 mg/dl to 80 ±31 mg/dl within 10 minutes of
infusion. In some cases hyperglycemia above 150 mg/dl was observed from 40 minutes of infusion.
Constant glucose infusion was found to be useful for elevation of glucose level... |
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- Case Report
- A Case of Autoimmune Hemolytic Anemia Caused by Warm Antibody.
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Sei Hee Choi, Mee Kyung Namgoong, Baek Keun Lim
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Clin Exp Pediatr. 1986;29(8):898-901. Published online August 31, 1986
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We reviewed a case of autoimmune hemolytic anemia caused by warm antibody in 7years old male patient. Diagnosis was established by clinical features, physical findings, laboratory findings, such as, CBC, Coombs’ test, fragility test, and bone marrow aspiration. Literatures were briefly reviewed.
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- Original Article
- Cord Plasma Alpha-Fetoprotein Values and Neonatal Jaundice.
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Mee Kyung Namgoong, Sei Hee Choi, Ae Sook Kim, Baek Keun Lim, Jong Soo Kim
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Clin Exp Pediatr. 1986;29(8):836-839. Published online August 31, 1986
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Alpha-fetoprotein(aFP) levels were studied in 20 neonatally hyperbilirubinemic children and 20 controls matched for gestational age. The mean aFP value of cord blood (119+58.2산g/ml) with hyperbilirubinemic children was significantly greater than that(79.6±40.8/zg/ml) for the control infants(P<0.001). At the age of 3 and 5 days the mean serum aFP in hyperbilirubinemic children were higher compared with the control group, the difference... |
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- A Measurement of Measles Antibodies among the Age Between 6 to 15 Months
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Ki Young Lee, Sang Woo Kim, Kyoung Tae Hwang, Kyu Chong Choi, Jong Soo Kim, Chang Ju Cho, Baek Keun Lim, Hyun Sook Kim, Dong Soo Kim
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Clin Exp Pediatr. 1986;29(4):375-380. Published online April 30, 1986
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To determine the proper age of the measles vaccination, we must know the time when the passively transferred measles antibody from mother disappeared. Because it can be a major factor for vaccine failure to take the measles vaccine to the children who still have the passive immunity. We measured the degree of immunity of 50 children with the age between... |
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- Case Report
- A Case of Eosinophilic Granuloma with Recurrent Bacterial Meningitis associated with CSF Rhinorrhea.
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Eung Deok Choi, Mee Kyung Namgoong, Seung Ha Yoo, Baek Keun Lim, Jong Soo Kim, Tae Seung Kim
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Clin Exp Pediatr. 1986;29(2):209-214. Published online February 28, 1986
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We experienced a case of eosinophilic granuloma with multiple lesions on skull, ribs, vertebrae, tibia
and pelvic bone. In addition, recurent bacterial meningitis was associated with CSF rhinorrhea probably due
to osteolytic lesion of eosinophilic granuloma in the same patient.
A brief review of literature was made.
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- Original Article
- Transcutaneous Bilirubin Measurements in Newborn Infants.
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Cook Huh, Soon Bock park, Baek Keun Lim, Jong Soo Kim, Duk Jin Yun
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Clin Exp Pediatr. 1985;28(4):314-324. Published online April 30, 1985
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Neonatal jaundice is probably the most frequently encountered diagnostic and therapeutic problem in the newborn, but its accurate assessment still requires a measurement of the serum bilirubin concentration. To date, repetitive and continuing blood sampling has been the only acceptable methodology available for monitoring the jaundiced newborn infant. This technique serves as a source of discomfort and of serious infection(Lilien... |
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- Case Report
- A Case of Preleukemia Presenting as Aplastic Anemia.
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Dong Hee Oh, Sei Hee Choi, Baek Keun Lim, Jong Soo Kim
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Clin Exp Pediatr. 1985;28(11):1141-1146. Published online November 30, 1985
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We experienced a case of preleukemia of 8-year-old male child, whose initial diagnosis was aplastic anemia, but 2 months later, acute lymphocytic leukemia was developed. So, we concluded that the initial state presenting as aplastic anemia had been prelekemia. Literatures were briefly reviewed.
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- A Case of Congenital Neuroblastoma.
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Soon Bock Park, Mi Sook Park, Baek Keun Lim, Jong Soo Kim, Kyi Beom Lee, Tai Seung Kim
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Clin Exp Pediatr. 1984;27(9):930-934. Published online September 30, 1984
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Neuroblastoma is the commonest malignant tumor identified during the neonatal period and the majority of neuroblastomas are felt to be congenital in origin. Neuroblastoma is a tumor of particular interest because it is known to arise from cells of the neural crest which possess the potential for maturation of spotaneous regression.
This report present the clinical, radiographic and autopsy findings of... |
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- A Case of Human Fascioliasis.
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Dong Hee Oh, Ae Sook Kim, Young Gun Kim, Baek Keun Lim, Jong Soo Kim, Yung Kyum Ahn
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Clin Exp Pediatr. 1984;27(8):827-831. Published online August 31, 1984
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We experienced a case of human fascioliasis in a 4-y-old male child who had been suffered from abdominal pain, pallor and intermittent generalized edema for about 21 months. Diagnosis was established by eggs of Fasciola species in stool and by double diffusion analysis. After treatment with bithionol, the symptoms were disappeared rapidly and the eggs also disappeared. A brief review... |
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- Original Article
- Clinical Studies of Aseptic Meningitis.
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Seung Ha Rheu, Soon Bok Park, Baek Keun Lim, Jong Soo Kim
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Clin Exp Pediatr. 1984;27(12):1176-1184. Published online December 31, 1984
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200 cases of aseptic meningitis were clinically observed for 171/2 years from 1966, Jan. to
1983, Jun. Eitologic classification showed that there were 165 cases (82.5%) of unknown
etiology because virus was not identified, 30 cases (15.0%) of mumps, and 5 cases (2.5%) of Kawasaki disease.
The most frequent age group was early childhood (81 cases, 40.5%) and more frequently in males (139... |
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- Case Report
- A Case of Holoprosencephaly.
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Cook Huh, Seung Ha Rheu, Young Gun Kim, Baek Keun Lim, Jong Soo Kim
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Clin Exp Pediatr. 1983;26(11):1125-1128. Published online November 30, 1983
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We experienced, a case of holoprosencephaly with no extracranial annormalities, normal
chromosme count and karyotype. The diagnosis was confirmed by brain C-T scan, which
was compatible to semilobar type of holoprosencephaly. The patient is living now at 2 years old.
Review of the references concerning holoprosencephaly was made briefly.
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- Original Article
- Clinical study of low birth weight infants.
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Sung Ho Chang, Young Gun Kim, Cook Huh, Baek Keun Lim, Jong Soo Kim
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Clin Exp Pediatr. 1982;25(9):898-905. Published online September 30, 1982
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A Clinical Study was made on. 542 low birth weight infants, admitted to the department
of pediatrics, Wonju Christian Hospital during 6 years from 1975 to 1980.
The results were as follows:
1) Incidence of low birth weight infants was 12.8% without sexual and seasonal predo-
migance, of which small for gestational age infants were about 50%.
2) Low birth weight infants were most prevalent among mothers... |
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- Clinical Study of Shigellosis.
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Young Gun Kim, Sung Ho Chang, Han Soo Choi, Baek Keun Lim, Jong Soo Kim
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Clin Exp Pediatr. 1982;25(7):723-729. Published online July 31, 1982
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Clinical and Bacteriological studies were carried out on 57 cases of infants and children with shigellosis who were cared from January, 1976 to December, 1980 in our hospital. The results were as follows: 1. The age distribution revealed the range between 6 months and 5 years(85% of all) with sex ratio of 30(53%) of male and 27(47%) of female, 1.1:1.... |
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- Case Report
- A Case of Acute(infantile) Gaucher's Disease.
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Baek Keun Lim, Kwan Sub Chung, Jae Seung Lee, Kir Young Kim, Byung Soo Kim, Duk Jin Yun, Chang Jin Kim, Chan Il Park
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Clin Exp Pediatr. 1981;24(10):982-990. Published online October 15, 1981
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A case of Acute infantile form of Gaucher's disease in Korean infant is described. The large cells characteristically found in the bone marrow and liver in Gaucher's disease have been investigated with electron microscope, as well as light microscope. The pertinent literature has reviewed briefly concerning the clinical and laboratory fingings, roentgenographic picture, pathogenesis, pathology, diagnosis and treatment of this... |
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- Original Article
- Clinical Studies on the Patent Ductus Arteriosus.
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Baek Keun Lim, Sung Kyu Lee, Duk Jin Yon, Seung Nok Hong
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Clin Exp Pediatr. 1980;23(10):798-808. Published online October 15, 1980
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Patent Ductus Arteriosus is one of the most common congenital heart diseases. The symptoms and clinical findings in patients with typical patnet ductus arteriosus are well recognized. That not all patient with ductus arteriosus have the typical clinical findings is well documented. Since the poor prognosis of untreated patent ductus arteriosus and good results of surgical intervention are fairly well... |
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