- Case Report
- Pseudoaneurysm after Renal Biopsy; Angigraphic Diagnosis and Treatment by Superselective Embolization
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Sin Weon Yun, Keun Seop Jung, In Seok Lim, Chul Ha Kim, Dong Keun Lee, Byeong Heun You, Hyung Jin Shim, Young Ku Kim
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Clin Exp Pediatr. 1995;38(3):417-421. Published online March 15, 1995
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The use of superselective embolization was assessed as a treatment for bleeding from arteriovenous fistulas and pseudoaneurysm after renal biopsy procedure. But unless it is sufficiently selective, the procedure results in loss of significant amount of renal parenchyme. We experienced one case of renal arterial pseudoaneurysm, which happened at 5days after percutaneous renal biopsy. Diagnosis of pseudoaneurysm was made by... |
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- A Case of Idiopathic Long QT Syndrome with 2:1 Atrioventricular Block
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Kwang In Lee, Chul Ha Kim, In Seok Lim, Dong Keun Lee, Byoung Hoon Yoo
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Clin Exp Pediatr. 1995;38(12):1701-1705. Published online December 15, 1995
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The idiopathic long QT syndrome is a very rare disorder in which affected individuals have an unusual electrocardiographic repolarization abnormality (QT prolongation) and a propensity to syncope and fatal ventricular arrhythmia.
Since Jervell and Lange-Nielsen first described this syndrome in 1957, progression has been made in the pathophysiology and in the treatment. Sinus bradycardia may be associated with this syndrome sometimes,... |
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- Original Article
- Clinical analysis of Serum and Urine N-Acetyl-β-D-Glucosaminidase (NAG) in Renal Disease
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Yo Han Chung, In Seok Lim, Chul Ha Kim, Byoung Hoon Yoo, Tae Sub Shim
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Clin Exp Pediatr. 1994;37(3):383-389. Published online March 15, 1994
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Recently, NAG activity has gained increasing importance as an aid in the diagnosis of renoparenchymal diseases. Elevation of urine NAG activity has been found to be an indicator of renoparenchymal diseases. To evaluate the diagnostic value of the NAG activity test in the renal disease, we carried out clinical study on 31 cases of renal disease patients who had been... |
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- Case Report
- A Case of Fanconi Syndrome
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Young Woon Lee, In Seok Lim, Chul Ha Kim
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Clin Exp Pediatr. 1993;36(5):737-442. Published online May 15, 1993
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Fanconi syndrome is a complex of renal tubular dysfunction defined by glycosuria without diabetes, generalized aminoaciduria, phosphaturia, bicarbonaturia, uric aciduria, and renal tubular acidosis. It is often associated with hypokalemia, hypophosphatemia, rickets and osteomalacia.
We have experienced one case of Fanconi syndrome with chronic tubulointerstitial nephritis. The patient was a 4 year and boy and his chief complaints were polyruia, polydipsia,... |
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- A Case of Roberts Syndrome
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Young Choi, Yo Han Chung, In Seok Lim, Chul Ha Kim, Dong Keun Lee, Seong Nam Kim, Sang Yong Song, Je Geun Chi
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Clin Exp Pediatr. 1993;36(10):1447-1451. Published online October 15, 1993
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Roberts syndrome is an autosomal recessive disorder accompanied by limb defects, craniofacial abnormalities, pre-and postnatal growth retardation. Patients with Roberts syndrome have characteristic premature separation of heterochromatin of many chromosomes and abnormalties in celldivision cycle.
We have experienced a case of Roberts syndrome in an immature neonate. The patients showed characteristic clinical features of multiple encephaloceles. Severe facial mid-line clefts, and... |
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- Original Article
- A case of malignant atrophic papulosis (Degos' disease).
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Sung Ku Lee, In Seok Lim, Chul Ha Kim, Dong Keun Lee, Eung Sang Choi, Byoung Hoon Yoo, Gae Yong Song
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Clin Exp Pediatr. 1991;34(12):1724-1729. Published online December 31, 1991
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Malignant atrophic papulosis (Degos’ disease) is characterized by porcelain-white skin lesions. It
has unknown etiology and bad prognosis. Death usually occurs from multiple intestinal perforations
weeks to years after onset.
We experienced a case of Degos’ disease in a 12-year-old male patient who had porcelain white
papules on face, trunk and extremities. Histopathologic studies showed broad epidermal necrobiosis
with thrombotic arteriolar occlusion.
A brief review of... |
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- A Case of Congenital Hypofibrinogenemia.
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Ji In Park, In Seok Lim, Chul Ha Kim, Byoung Hoon Yoo
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Clin Exp Pediatr. 1990;33(7):1009-1011. Published online July 31, 1990
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Congenital hypofibrinogenemia is a rare congenital bleeding disorder, inherited by autosomal
dominant or recessive trait.
We experienced one case of congenital hypofibrinogenemia in 4 year-old female patient with chief
complaints of headache and ecchymosis. History of continuous umbilical cord bleeding and frequent
bleeding tendency against minor trauma were revealed on her past medical history. On laboratory
data, bleeding time, platelet aggregation test were normal and... |
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- Echocardiographic Evaluation of Sequential Change of Cardiac Function in Normal Neonates.
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Ji In Park, Chul Ha Kim, Byoung Hoon Yoo
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Clin Exp Pediatr. 1990;33(11):1533-1539. Published online November 30, 1990
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Echocardigraphy was done on the first and the second day of life in 23 normal full term newborns
to evaluate the sequential change of cardiac function of the normal neonates.
The results were as follows.
1) On the first day of life, all of the measurements of diastolic filling except peak A velocity were
significantly different when the right and left ventricle were compared. For... |
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