- Original Article
- A clinical study of deep neck abscess in children
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Soo Jung Lee, Mee Yong Shin, Chang Hwi Kim, Yoon Woo Koh
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Clin Exp Pediatr. 2007;50(4):363-368. Published online April 15, 2007
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Purpose : It has been reported that deep neck abscesses are recently increasing again. We analyzed pediatric cases with deep neck abscesses during the last several years to contribute to the treatment of the disease.
Methods : The clinical data of 30 children under 16 years of age with deep neck abscess from February 2001 to July 2006 were analysed retrospectively.... |
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- Childhood Obstructive Sleep Apnea Syndrome :
Clinical and Polysomnographic Findings
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Yang Jun Park, Dae Kyun Koh, Jin Hee Oh, Soo Jung Lee
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Clin Exp Pediatr. 2001;44(7):786-795. Published online July 15, 2001
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Purpose : Although pediatricians may see a lot of patients with clinically suspected obstructive sleep apnea syndrome(OSAS), the actual incidence, clinical and polysomnographic manifestations of OSAS in children have not well been recognized and reported cases are rare. The objective of this study was to evaluate the efficacy of polysomnography in the diagnosis of OSAS in children and to analyze... |
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- Case Report
- A Case Of Common Variable Immunodeficiency with Fatal Measles
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Su Jin Cho, So Hyun Kim, Soo Jung Lee, Kyung Ha Yoo, Kyung Hyo Kim
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Clin Exp Pediatr. 2001;44(12):1463-1468. Published online December 15, 2001
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Common variable immunodeficiency(CVID) is a heterogeneous immunodeficiency syndrome characterized by hypogammaglobulinemia, recurrent bacterial infections, and a variety of immunological abnormalities. We report a 10-year-old boy diagnosed with CVID and a fatal case of measles. He was admitted for fever, cough, conjunctival injection with purulent discharge and maculopapular rash with some scattered pinpoint sized petechial lesions on the whole body for... |
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- Dapsone in a Case with Chronic Recurrent Henoch-Schönlein Purpura
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Jin Choi, Soo Jung Lee, Dae Kyun Koh
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Clin Exp Pediatr. 1999;42(11):1574-1578. Published online November 15, 1999
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The most clearly delineated condition with prominent cutaneous leukocytoclastic vasculitis which presents to a pediatrician is Henoch-Schönlein purpura. There is general agreement that in Henoch-Schönlein syndrome the skin manifestations have a very benign long-term course and that corticosteroids are of little value. Dapsone appears to be of special value in diseases characterized by an accumulation of polymorphonuclear neutrophils notably leukocytoclastic... |
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- Follow up of a Case of Primary Intestinal Lymphangiectasia
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Su Jeong Ha, Soo Jung Lee, Dae Kyun Koh
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Clin Exp Pediatr. 1999;42(10):1452-1458. Published online October 15, 1999
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Primary intestinal lymphangiectasia is a rare congenital disorder characterized by diffuse or localized ectasia of the enteric lymphatics, often in association with lymphatic abnormalities elsewhere in the body. The pathogenesis of these abnormal lymphatic structures is uncertain. Ectatic lymphatics may be located in the mucosa, submucosa, or subserosa, leading to a loss of protein and lymphocytes into the gut or... |
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- A Case of Intestinal Necrosis Associated with Henoch-Schönlein Purpura
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Soo Jung Lee, Young Yoo Kim, Sung Soo Whang, Kyung Yil Lee, Won Ik Lee, Jeong Soo Kim, Chang Joon Ahn, Mi Kyung Jee
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Clin Exp Pediatr. 1992;35(9):1291-1297. Published online September 15, 1992
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Gastrointestinal symptoms of Henoch-Schönlein commonly present abdominal pain, nausea, nomitting, melena and hematemesis and resolve mostly without any complications. Some times life threatening gastrointestinal manifestations such as massive hemorrhage, intussusception, intestinal necrosis and perforation may develop
We report a case of the Henoch-Schönlein purpura with intestinal lesion in 11 year female patient who presented with colicky abdominal pain and bloody stool... |
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- A Case of Congenital Pelger-Huet Anomaly
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Soo Jung Lee, Young Yoo Kim, Seung Won Kang, Jong Wan Kim, Kyung Tai Whang, Sung Ho Cho
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Clin Exp Pediatr. 1992;35(11):1578-1583. Published online November 15, 1992
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Congenital Pelger-Huet anomaly is an autosomal dominant disorder characterized by incomplete nuclear segmentation of neutrophils without functional disturbance. The morphology of these mature but hyposegmented neutrophils may be confused with that of immature neutrophils (bands), thereby suggesting bacterial infection.
We experienced a case of congenital Pelger-Huët anomaly on routine hematologic examination in a 7-year old boy who was admitted because of... |
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