1.Bizarre Parosteal Osteochondromatous Proliferation: A Report of One Case
Yung Khee CHUNG ; Jung Han YOO ; Dong Hyeon LEE
The Journal of the Korean Orthopaedic Association 1990;25(2):602-605
In 1983, Nora et. al. reperted 35 cases of bizarre parosteal osteochodromatous proliferations of the hands and feet. All lesions occured on proximal phalanges, metatarsals, or metacarpals. The gross appearance was typically that of a small osteochondroma. Radiologically, the proliferations lacked both central continuity of the tumor with the underlying osseus medulla and flaring of the adjacent cortices. Histologically, the lesion exhibited marked proliferative activity, irregular bohy cartilaginous interface, and enlarged, bizarre, and binucleate chondrocyte. The authors experienced a case of bizarre parosteal osteochondromatous proliferation of the right foot in a 61 year-old female which arised from the proximal phalanges of second toe, hostologic and radiologic findings were consistent with the bizarre parosteal osteochondromatous proliferation. The mass was treated by excision, and neither recurrence, nor malignant change was observed up to one year follow-up period.
Chondrocytes
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Female
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Follow-Up Studies
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Foot
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Hand
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Humans
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Metacarpal Bones
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Metatarsal Bones
;
Osteochondroma
;
Recurrence
;
Toes
2.Overgrowth of the Tibial Shft following Fracture in Children
Yung Khee CHUNG ; Jung Han YOO ; Dong Hyeon LEE
The Journal of the Korean Orthopaedic Association 1990;25(3):787-793
Longitudinal growth acceleration of the femoral shaft after fracture in children has been recognized since the late nineteenth century, Orthopaedic surgeons have attempted to compensate for the leg length discrepancy by allowing union to occur with some degree of shortening, but logitudinal overgrowth following fractures of the tibial shaft in children has been rarely studied. Thirty-one children, treated for fracture of the shaft of tibia, were studied prospectively to assess the consequent increase in longitudinal growth of the tibia. The material presented in this paper is the result of the study of thirty-one children with fractured tibia who were treated in the Department of Orthopaedic Surgery of Kangnam Sacred Heart Hospital of Hallym University, since 1986 October, the age of the child varied from 3 years to 13 years, these cases have been followed from 30 months to 40 months. We have made a radiologic study of fracture of the tibial shaft with a view to analysing the results according to a number of factors, including the sex and the type, site and degree of overriding of fracture, and method of treatment, and then the degree of overgrowth was compared with unaffected side. 1. The average tibial overgrowth following tibial shaft fracture is 7mm. 2. Growth of the femur was not affected by the tibial fracture.
Acceleration
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Child
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Femur
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Heart
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Humans
;
Leg
;
Methods
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Prospective Studies
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Surgeons
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Tibia
;
Tibial Fractures
3.Effect of fluid restriction on postnatal weight and outcome in very low birth weight infants.
Chul LEE ; Hyeon Soo LEE ; Ran NAMGUNG ; Dong Gwan HAN
Journal of the Korean Pediatric Society 1991;34(3):348-354
No abstract available.
Humans
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Infant*
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Infant, Very Low Birth Weight*
4.Effect of fluid restriction on postnatal weight and outcome in very low birth weight infants.
Chul LEE ; Hyeon Soo LEE ; Ran NAMGUNG ; Dong Gwan HAN
Journal of the Korean Pediatric Society 1991;34(3):348-354
No abstract available.
Humans
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Infant*
;
Infant, Very Low Birth Weight*
5.An operative treatment of osteogenic sarcoma.
Soo Bon HAHN ; Nam Hyeon KIM ; Dae Youn HAN ; Chang Dong HAN ; Weon Ik LEE
The Journal of the Korean Orthopaedic Association 1993;28(3):1249-1260
No abstract available.
Osteosarcoma*
6.The clinical studies on acute poisoning of infants and children visited the emergency room in rural area.
Chang Hi LEE ; Gyu Dong CHOI ; Hyeon Soo HAN ; Hye Heon HWANG ; Myung Ho CHO
Journal of the Korean Academy of Family Medicine 1991;12(2):40-46
No abstract available.
Child*
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Emergencies*
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Emergency Service, Hospital*
;
Humans
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Infant*
;
Poisoning*
7.Association between Tardive Dyskinesia and 267C/T Polymorphism of 5-HT6 Receptor Gene in Schizophrenia.
Sang Woo HAN ; Dong Hyeon KIM ; Yong Ho JUN
Journal of the Korean Society of Biological Psychiatry 2004;11(1):54-60
OBJECTIVES: Tardive dyskinesia(TD) is a serious side effect associated with long-term antipsychotic treatments. Some candidate genetic polymorphisms were reported to be associated with TD and possible involvement of serotonergic receptors in the pathophysiology of TD has been suggested. In the present study, we investigated the association between 5-HT6 receptor gene polymorphism and TD with schizophrenia. METHODS: To investigate the relationship between 5-HT6 receptor gene polymorphism and TD, 60 patients with TD were compared with 60 patients without TD. The 267C/T allele of 5-HT6 receptor gene was genotyped by means of polymerase chain reaction method. TD was evaluated using the Abnormal Involuntary Movement Scale(AIMS). RESULTS: The patients with the three 267C/T genotype showed no significant differences in age, gender, and duration of illness. No significant difference in genotype frequencies was observed between schizophrenic patients with and without TD. In addition, there was no difference in allele frequencies. Further analysis with an measure of AIMS scores showed that these scores were not significantly influenced by the 5-HT6 receptor gene polymorphism. CONCLUSION: These results suggest that 267C/T polymorphism of 5-HT6 receptor gene is not significantly associated with susceptibility to TD in schizophrenia.
Alleles
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Dyskinesias
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Gene Frequency
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Genetics
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Genotype
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Humans
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Movement Disorders*
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Polymerase Chain Reaction
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Polymorphism, Genetic
;
Schizophrenia*
;
Serotonin
8.A case with unusual manifestation of multiple amebic liver abscesses by coinfection with clonorchis sinensis-diagnosed by CT-guided fine needle aspiration.
Sung Sook KIM ; Jung Ran KIM ; Hyeon Kyeng LEE ; Sung Hee LEE ; Dong Sun HAN ; Sung Tae HONG
Korean Journal of Cytopathology 1993;4(2):176-180
No abstract available.
Biopsy, Fine-Needle*
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Coinfection*
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Liver Abscess, Amebic*
9.A case of congenital anomaly in robertsonian translocation carrier pregnance.
Myung Cheol KIM ; In Bai CHUNG ; Hyeok Dong HAN ; Hyeon Chul KIM ; Dae Hyun KIM ; Kun Chang SONG
Korean Journal of Obstetrics and Gynecology 1993;36(7):3186-3191
No abstract available.
10.Infrahepatic interruption of inferior vena cava
Yeon Hyeon CHOE ; Dong Ho LEE ; Young Goo KIM ; Jae Hyung PARK ; Kyung Mo YEON ; Man Chung HAN
Journal of the Korean Radiological Society 1986;22(1):124-130
Congenital anomaly of IVC is rare, but understanding of this anomaly is important in radiological diagnosis,angiographic procedures and major retroperitoneal and thoracic surgery. We analysed 23 cases of IVC interruptiondiagnosed by cardiac angiography at Seoul National University Hospital. The results were as follows: 1. Theincidence of infrahepatic interruption of IVC was 0.45% of the patients having cardiac angiography and mostpatients showed cyanosis(91%). 2. The most common associated cardiac anomaly was right ventricular outflow tractobstruction (60%). Other associated cardiac defects were VSD, ASD, valvular anomaliesin 9 cases(39%) respectively;double outlet right bentricle, bilateral superior vena cava, single ventricle in 6 cases(26%) respectively; singleatrim, PDA in 5 cases(22%) respectively. 6 cases of situs inversus, 3 cases of situs ambiguus,2 cases of visceralheterotaxia and one case of asplenia were observed also. 7 cases of left-sided IVC were associated with IVCinterruption in normal situs.
Angiography
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Humans
;
Seoul
;
Situs Inversus
;
Thoracic Surgery
;
Vena Cava, Inferior
;
Vena Cava, Superior