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小兒에서 反復되는 腹痛 頭痛 및 四肢痛에 대한 臨床的 觀察
宋貞玉 고려대학교 의과대학 1975 고려대 의대 잡지 Vol.12 No.1
The complaints of recurrent abdominal pain, headache, and limb pains either separately or in combination have been investigated in a non-selected population of the children who visited to the Woo-Sok Hospital Korea University College of Medicine froma January 1971 to June 1974. Through the analysis of 6,824 children, that is, 3,995 boys and 2,819 girls, the following results were obtained: All these complaints, either separately or in combination, occurred more frequently in girls than boys. The occurrence of abdominal pain was 2.28% in boys and 6.95% in girls and reached a maximum rates of 10.66% at 13 years of age in boys and 15.44% at 11 years of age in girls. Headache was complained in an average occurrence of 2.18% in boys and 4.15% in girls and reached a maximum rates of 11.48% at the age of 13 years in boys and 15.04% at the age of 12 years in girls. In boys, the complaint of limb pains was in 2.9% and in 3.8% in girls and reached a maximum rates of 7.75% at 12 years of age in boys while in girls a maximum rates of 9.37% was reached at the age of 14 years. The painful conditions more frequently occurred in school children, first born child, body weight over 75 percentile, and monosymptomatically (86%). Various combinations of above complaints were noted only in 14% of total cases studied.
崔昌姬,宋貞玉,洪榮義,李鉉金 최신의학사 1975 最新醫學 Vol.18 No.1
Juvenile myasthenia gravis is a relatively rare disease in childhood. Recently, we experienced a case of Juvenile myasthenia gravis in an 8-year 8 months old girl who was admitted to our Dept of Ped. of Woo-Sok Hospital. She has longstanding history of symmetrical ptosis since 20 months of age. There is no history of similar illness in the family, patient was treated successfully by Neostigmine and we report this case with reviews of literatures.
權澤孚,宋貞玉,申東春,林正均 최신의학사 1976 最新醫學 Vol.19 No.4
Chronic myelocytic leukemia is one of rare type of leukemia in childhood. Frequent presenting initial symptoms are intermittent fever with unknown origin, abdominal distention, .hepatosplenomegaly, bleeding tendency, recurrent infection and generalized lymphadenopathy. The case was ten years old male child who was admitted with symptoms of abdominal distention, fever, and hepatosplenomegaly. He was confirmed by bone marrow aspiration and hematologic studies. We reviewed the literature about the etiology incidence, clinical symptoms, physical findings, hematologic findings, prognosis and management of chronic myelocytic leukemia briefly.