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Case Report
A Case of Congenital Hypertrophic Pyloric Stenosis in Two Siblings
Yung Min Jang, Mi Ran Park, Sung Yoon Byun, Jae Young Kim, In Sang Jeon, Kwang Jun Kim
Clin Exp Pediatr. 1993;36(7):1025-1029.   Published online July 15, 1993
Original Article
A Case of Toxic Epidermal Necrolysis.
Eun Hwa Shin, Youn Hong Choi, Ju Hong Cha, Kwang Jun Kim, Kyung Je Sung
Clin Exp Pediatr. 1988;31(8):1079-1084.   Published online August 31, 1988
Toxic Epidermal Necrolysis is uncommon disease characterized by erythema and shedding of the epidermis and mucous membrane. Mortality rates are high. The reaction is probably a drug-induced hypersensitivity phenomenon. We experienced Toxic Epidermal Necrolysis in a 4 yr old boy whose skin lesion had developed 3 days after taking medication from a drug store for common cold. Diagnosis of TEN was established by clinical...
A Case of Kasabach-Merritt Syndrome.
Eun Hwa shin, Youn Hong Choi, Ju Hong Cha, Kwang Jun Kim
Clin Exp Pediatr. 1988;31(7):935-941.   Published online July 31, 1988
Kasabach-Merritt Syndrome is a combination of a rapidly enlarging hemangioma and throm- bocytopenia. A 5 day old male newborn who had giant hemangioma associated with thrombocytopenia and anemia is reported with review of literatures. He was placed on prednisolone, blood transfusion, and compression with the elastic bandage over hemangioma. Hemangioma has been somewhat regressed, bleeding tendency has been improved, however, platelt counts are still low.
Two Cases of Agranulocytosis induced by Acetanilid and Dilantin
Kwang Jun Kim, Mi Ja Shin, Kyung Shuk Yang
Clin Exp Pediatr. 1972;15(1):63-69.   Published online January 31, 1972
We experienced 2 cases of agranulocytosis induced by acetanilid and dilantin in Dept, of Pediatrics of Seoul Red Cross Hospital in 1971. One who was a 8 year old boy showed complete recovery, clinically as well as in hematologic aspects within one week after discontinuation of dilantin medication by which agranulocytosis was thought to be induced. Bone marrow aspiration performed on recovery showed myelocytic...
A Case of Congenital Syphilis Associated with Multiple Destruction, Fracture of Bone and Pseudoparalysis
Myung Jin Koo, Kwang Jun Kim, Kyung Shuk Yang
Clin Exp Pediatr. 1971;14(12):580-583.   Published online December 31, 1971
A case of congenital syphilis associated with multiple destructions and fractures of bones in a 3 month-old male infant is reported. He had fractures of both humeri, and multiple osteolytic lesions, noted on both femurs, humeri, tibiae, radii, ulnae, frontal bone of skull, metacarpal and 4th proximal phalanx and also developed pseudoparalysis of right lower extremity. Diagnosis was confirmed by...
Case Report
Three Cases of Congenital Syphilitic Nephrotic Syndrome
Kwang Jun Kim, Myung Jin Koo, Kyung Shuk Yang
Clin Exp Pediatr. 1970;13(6):359-364.   Published online June 30, 1970
Three eases of congenital syphilitic nephrotic syndrome are presented. This is the first report, to our knowledge, in Korea. It is our opinion that the diagnosis of congenital syphilitic nephrotic syndrome is highly probable in case I and HI. Although there were no edema and hypopreteinemia in case I, we believe that the congenital syphilis involved the kindey according to...
A Case of Kasabach-Merritt Syndrome
Kwang Jun Kim, Jung Sik Kim, Kyung Shuk Yang
Clin Exp Pediatr. 1969;12(9):523-526.   Published online September 30, 1969
A case of Kasabach-Merritt syndrome in a 2 month-old male infant was presented. The diagnosis was confirmed by physical, peripheral blood and biopsy findings. Slight improvement was observed within about 2 weeks of parenteral administration of prednisolone, 20 mg, daily, but after reduction to 15 mg of prednisolone per day, the hemangioma enlarged and the platelets count decreased below 30,...