- Case Report
- A Case of Subacute Necrotizing Lymphadenitis.
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S Y Song, W H Kwon, C H Han, H R Chung, S Y Kim, Y D Kwon
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Clin Exp Pediatr. 1990;33(5):714-720. Published online May 31, 1990
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We experienced a case of subacute necrotizing lymphadenitis in a 6 year old boy which has been
originally described in Japan.
The diagnosis was made by clinical features(fever, adenopathy), laboratory(WBC, ESR, GOT, GPT,
LDH etc), histopathologic, electron microscopic, and immunohistologic findings.
The review of literature was made. |
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- Original Article
- 2 cases of I-cell disease.
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H D Lee, K H Kim, Y T Lim, W T Kim, S Y Kim, H J Jeon, H J Park, C Y Kim
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Clin Exp Pediatr. 1990;33(3):360-366. Published online March 31, 1990
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Clinical pictures of 2 cases with I-cell disease patients, 8 and 11 months old female, were analyzed.
Characteristic coarse facial features, gum hypertrophy, retarded growth and dysostosis multiplex
were observed in both cases. Under phase contrast microscopic examination, cultured fibroblasts of
skin of case I patient had their cytoplasm filled with numerous dark granules leaving only a
juxtanuclear crescent free of inclusions. We report... |
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- A Clinical study on the Neonatal Exchange Transfusion.
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S Y Song, W H Kwon, C H Han, H L Jeong, S Y Kim, Y D Kwon
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Clin Exp Pediatr. 1990;33(2):162-169. Published online February 28, 1990
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A clinical observation was performed on patients with neonatal hyperbilirubinemia who were
treated by exchange transfusion, and following results were obtained. Exchange transfusion was
performed in 31 cases (8% of 383 csases admitted due to neonatal hyperbilirubinemia during the
observation period).
There was no sex predominance (male 16, female 15). Most common type of delivery was normal
varginal delivery (22 cases, 71%).
Birth weight of 17... |
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- A Case of Virginal Breast Hypertrophy.
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S C Hamm, S W Oh, S S Shim, H D Lee, S Y Kim, H J Park, H J Jun, C Y Kim
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Clin Exp Pediatr. 1990;33(12):1741-1747. Published online December 31, 1990
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A 12-year-old girl visited due to massive breast enlargement during past 10 months. We evaluated
hormonal levels and radiologic studies but could not find the cause and diagnosed as virginal or
juvenile breast hypertrophy. Hormonal therapy was not effective. We relieved her physical discom-
fort or mental anguish with reduction mammoplasty and report with brief review of related literatur-
es. |
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- Clinical Study on Twins.
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C H Han, W H Kwon, H R Jung, S Y Kim, Y D Kwon
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Clin Exp Pediatr. 1989;32(3):331-341. Published online March 31, 1989
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We observed 150 twin cases over 26 weeks gestational age among 8,328 deliveries which were born
from 75 Korean twin pregnancies at Catholic Hospital. Taegu during 5 years from Jan. 1981 to Dec.
1985. retrospectively.
We investigated survey of twin delivery on various aspects as same manner as singletons. which
was incidence of twin deliveries, body weight with gestational age, body weight difference between
co-twins,... |
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- Waardenburg's Syndrome in a Boy and Mother.
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D H Kim, M Y Kim, C S Suh, S Y Kim, J Y Jung
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Clin Exp Pediatr. 1988;31(5):655-659. Published online May 31, 1988
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Waardenburg's syndrome is a rare autosomal dominant disorder which is characterized by (1)
lateral displacement of the medial canthi of the eyes and the inferior lacrimal puncta.
(2) a broad, prominent root of the nose (3) hyperplasia of the medial portions of the eyebrows (4)
white or grey forelock (5) partial or total heterochromia of the irides and (6) deaf-mutism.
The authors experienced 2... |
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- Three Cases of hereditary Spherocytosis.
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D H Kim, M Y Kim, S Y Kim, J Y Jung
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Clin Exp Pediatr. 1988;31(4):500-505. Published online April 30, 1988
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We experienced 3 cases of herediatry spherocytosis which occurred in a family. The family consited
of parents, one sone and one daughter.
The case I, Daughter showed the chief complaints of pallor ad generalized weakness.
The case II, Son hoswed the chief complaint of jaundice.
The case III, Father showed the chief complaints of fatigue and dizziness.
Diagnosis was made by presence of spherocytes in... |
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- Case Report
- A Case of Gaucher's Disease.
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J S Kim, S J Kim, H J Suh, I J Kang, S Y Chung, J B Park, S K Moon, S Y Kim
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Clin Exp Pediatr. 1986;29(9):1028-1034. Published online September 30, 1986
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We experienced a case of adult type Gaucher's disease in 14 month old male.
The patient showed hepatosplenomegaly with anemia and characteristic Gaucher cells in bone marrow aspiration and biopsy of liver and spleen both in light microscopic and electromicroscopic examination. Splenectomy was followed by improvement of anemia and thrombocytopenia but hepatomegaly remained even progressed.
A brief review of literature was... |
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- Caroli's disease.
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K H Suh, S K Chai, S W Lee, S M Shin, C I Ahn, S Y Kim
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Clin Exp Pediatr. 1979;22(5):384-390. Published online May 15, 1979
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Congenital dilatation of the biliary tract(Caroli's disease) is uncommon condition. The condition was first described by Caroli and associates in 1958. The location, degree and type of dilatation vary. The disease entity is characterized by: (1) congenital saccular dilatation of the intrahepatic bile ducts; (2) high incidence of stone formation and cholangitis; (3) absence of hepatic cirrhosis and portal hypertensin;... |
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