- Original Article
- A Case of multiple Splenic Abscess.
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J H Kim, Y H Kim, J O Lee, E R Kim, S J Lee
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Clin Exp Pediatr. 1989;32(2):244-249. Published online February 28, 1989
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The authors experienced a case of multiple splenic abscess in 3 years old girl with a chief complaint
of fever, anorexia and abdominal pain for 2 months.
The abscess cavity was detected by abdominal ultrasonography and computerized axial tomography.
Computerized axial tomography appeared as a multiple round low density areas in the spleen.
Abdominal ultrasonography appeared as poorly defined focal decreased echoes in the... |
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- 11 q Deletion Syndrome.
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Y B Im, S B Park, B Y Pyun, J O Park, S J Lee, S Y Moon
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Clin Exp Pediatr. 1989;32(2):239-243. Published online February 28, 1989
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llq deletion syndrome is a rare chromosomal anomaly.
The authors experienced a case of llq deletion syndrome with congenital glaucoma and infantile
spasm in a female child. She showed delayed psychomotor development, flat occiput, hypertelorism,
low set malformed ears, flat nasal bridge, short neck, simian line on right palm and throm.
bocytopenia.
Chromosomal study showed the deletion of the long arm of chromosme 11, karyotypically... |
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- Clinical Studies of Childhood Typhoid Fever during Outbreak.
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Y M Choung, H K KIM, B T Kim, S C Park, Y C Kim, H J Cha, S J Lee
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Clin Exp Pediatr. 1989;32(10):1345-1352. Published online October 31, 1989
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During 2 months from April 1988 to May 1988 when typhoid fever outbreak occured in the hot
spring resort town, 52 cases of typhoid fever had been admitted to the department of Pediatrics Soon
Chun Hyang Chun An Hospital, and evaluated clinically. The results were summarized as follows.
1) Among the 52 cases of typhoid fever, 28 were male and 24 were female. The... |
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- Angioimmunoblastic Lymphadenopathy in a Child.
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S J Lee, H S Lee, H S Kim, C M Kang, D S Kim
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Clin Exp Pediatr. 1988;31(12):1669-1673. Published online December 31, 1988
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Angioimmunoblastic lymphadenopathy is a lymphoma like disorder consisting of generalized
lymphadenopathy, hepatosplenomegaly, skin rashes, often associated with dysgammag-
lobulinemia.
We have experienced recently 3 year old female complaining of generalized lymphadenopthy,
fever, hepatomegaly and hypergammaglobulinemia, and was proved as angioimmunoblastic
lymphadenopathy histologically.
Patient was treated with combined chemotherapy with COMP and responded well clinically in 4
months.
The brief review of the literature was made. |
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- Perforation of the Gastointestinal Tract in Infancy and Childhood.
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S J Lee, Y S Kim, H D Cha, T C Kwon, C M Kang
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Clin Exp Pediatr. 1988;31(12):1626-1632. Published online December 31, 1988
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Thirty-nine patients with perforations of the gastrointestinal tract proved by operation were
presented.
35.9% of perforations were between the age of 6-10 year and 20.5% were Neonates.
Male to female ratio was 2:1.
The cardinal symptom of the perforation was abdominal pain in older child and abdominal
distention in the neonates.
Abdominal X-ray showed subphrenic free air shadow in 48.7% of the total cases.
The subphrenic free... |
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- Status of Pediatric Disease in Korea.
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H J Oh, J H Lee, S B Lee, S I Lee, J Y Choi, S J Lee, K S Jung, Y C Tockgo
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Clin Exp Pediatr. 1987;30(5):469-486. Published online May 31, 1987
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It is the purpose of this study to help understand the disease pattern in the pediatric f
The survey was made mostly by the Korean Pediatric Association during the period o
1983 to 1984 with the help from 43 pediatric training hospitals throughout Korea.
The studies were made from the total of 67,550 pediatric inpatients under 15 years of s
the distribution of the... |
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- A Clinical Observation of Acute Carbon Monoxide Poisoning.
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M R Roh, K W Lee, E M Kim, S M Shin, S J Lee
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Clin Exp Pediatr. 1984;27(12):1213-1217. Published online December 31, 1984
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Carbon monoxide poisoning is one of the most serious public health problem in Korea.
Author analysed 126 cases of pediatric CO poisoning which had been treated in emergency
room of Soon Chun Hyang Hospital, during 4 years from Jan. 1979 to Decern. 1983.
The results are as follows:
1) Incidence in male was similar to that in female and the age group between 11 〜... |
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- Case Report
- A Case of Chronic Granulomatous Disease.
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C H Park, M R Roh, S C Park, J O Park, D H Lee, S J Lee
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Clin Exp Pediatr. 1984;27(11):1141-1146. Published online November 30, 1984
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Chronic granulomatous disease is characterized by an inability of patients* leukocytes to
generate hydrogen peroxide and to kill non-peroxide forming bacteria, such as staphylococci,
E. coli and serratiae etc.
We experienced a case of chronic granulomatous disease with recurrent pyogenic infection.
It was diagnosed by clinical findings and laboratory examinations including NBT test. Clin-
ical findings showed persistent diarrhea since birth, recurrent bacterial pneumonia, perianal
abscess,... |
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- A Case of Osteopetrosis.
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C H Park, J H Yoo, T K Yoon, J O Park, S J Lee
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Clin Exp Pediatr. 1983;26(12):1203-1208. Published online December 31, 1983
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Osteopetrosis is a rare disease causing an abnormal sclerosis of bone.
We experienced a case of osteopetrosis with rachitic-like changes which was diagnosed by
clinical features, radiologic examinations and laboratory examinations. Radiologic examinations showed generalized sclerosis, dense orbital roof, thick & dense skull base, anterior notching “sandwich” appearance of the vertebrae, club shaped long bone, and bone within bone appearance in metacarpals.... |
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- Fanconi's Anemia.
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J H Yoo, E M Kim, S J Lee, W B Kim, D W Lee, D Y Kang, K Y choi
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Clin Exp Pediatr. 1983;26(11):1139-1144. Published online November 30, 1983
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We report 1 case of Fanconi’s anemia which has severe pancytopenia, increased fetal Hb,
hyperpigmented skin, absence of right thumb and metacarpal bone, retardation of bone age
and chromosomal abnormalities with a brief review of related literature and references.
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- One Case of 13q-Syndrome.
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C O Lee, T H Lee, D W Lee, S J Lee, D.W Lee, D.Y Kang, K.Y Choi, Je G Ghi
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Clin Exp Pediatr. 1982;25(7):743-747. Published online July 31, 1982
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13 q-syndrome based on loss of specific band was first described by Bain and Gauld in 1963 and may be transmitted if one parents is translocation carrier. We experienced one case of 13p-syndrome with ercephalocele in newborn diagnosed by clinical feature, chromosomal study and autopsy findings. He had multiple anomalies such as microcephaly, hypertelorism, microphthalmia, absent thumbs, clinodactyly, equinovarus, bifid... |
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- Two Cases of Cryptococcosis.
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T K Yoon, J S Moon, D H Lee, S J Lee
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Clin Exp Pediatr. 1982;25(2):195-199. Published online February 28, 1982
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We experienced two cases of cryptococcosis which were diagnosed by India-ink stain and culture of cerebrospinal fluid and biopsy with culture of skin lesion or lymph nodes. Both cases were confused with tuberculous meningitis or miliary tuberculosis because of irregular densities in hilum and scattered miliary sized nodules in chest X-ray, family history of pulmonary tuberculosis and clinical symptoms. We... |
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- A case of Pneumothorax due to Paragonimiasis with Family.
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S J Han, B Y Pyun, D H Lee, S J Lee
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Clin Exp Pediatr. 1982;25(2):168-174. Published online February 28, 1982
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We experienced one case of pneumothorax due to paragonimiasis of 6 years aged girl. The diagnosis was established by characteristic feature of ova on stool and sputum. A brief review of related literature was presented. |
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- The Kocher-Debre-Semelaigne Syndrome.
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M Y Chung, S I Kwon, S J Lee, D H Kum
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Clin Exp Pediatr. 1982;25(1):92-96. Published online January 31, 1982
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A 4-year old girl with the Kocher-Debre-Semelaigne syndrome, hypothyroidism with generalized muscular hypertrophy is described. Histologic examination of a calf muscle showed musclular hypertrophy with focal eosinophilic degeneration. The stigmas of hypothyroidism and the muscular hypertrophy disappeared promptly and concomitantly following therapy with desiccated thyroid. Similar cases reported in literature are briefly reviewed. The clinical and histologic changes of the... |
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- Original Article
- A Clinical Study on Anaphylactoid Purpura.
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T K Yoon, T H Lee, S M Shin, S J Lee
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Clin Exp Pediatr. 1981;24(12):1185-1192. Published online December 15, 1981
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Anaphylactoid purpura is a common disease in childhood and manifests variable clinical features including hepatomegaly. We analyzed 35 children who were admitted and diagnosed as anaphylactoid purpura at Soon Chun Hyang hospital during the periods of 5 years from September, 1975 to August 1980. The results were as follows: 1)It more frequently affected male than female, in the ratio... |
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- Gastroschisis ; Two cases report & review of the literature.
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S Jung, J H Park, S J Lee, D H Keum, S D Pae
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Clin Exp Pediatr. 1980;23(7):586-589. Published online July 15, 1980
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Gastroschisis is relatively rare congenital malformation and requires a surgical emergency in Newborn infant. We experienced two survival cases of gastroschisis, which was treated surgically and has grown up normal and healthy. This report is concerned with our experience of the survival cases and reviewed the embryology, pathology and the current concepts in the management of gastroschisis in the literatures. |
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