1.The treatment of unicameral bone cyst by topical injection of methylprednisolone acetate.
Sung Joon KIM ; Kuhn Sung WHANG ; Kyeong Jin CHOI
The Journal of the Korean Orthopaedic Association 1992;27(4):1108-1116
No abstract available.
Bone Cysts*
;
Methylprednisolone*
2.Replantation of the amputated finger tip.
Jin Soo KIM ; Jong Ick WHANG ; Sung Ho YOON
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1992;19(6):1069-1070
No abstract available.
Fingers*
;
Replantation*
3.A Case of Confluent and Reticulated Papillomatosis: Treatment with Etretinate.
Jin Woo PARK ; Tae Sung BU ; Sung Yul LEE ; Jong Suk LEE ; Kyu Uang WHANG
Korean Journal of Dermatology 1998;36(6):1103-1105
Confluent and reticulated papillomatosis(CRP) is a rare dermatosis. The lesions are hyperkeratotic, verrucous papules and plaques, resulting in a confluence of lesions centrally and a reticulated pattern at the periphery. It is more common in women and during puberty. The histopathological findings show papillomatosis, hyperkeratosis and a sparse superficial perivascular lymphocytic infiltrate. We report a case of CRP that responded to oral etretinate in an 18-year-old man.
Acitretin*
;
Adolescent
;
Etretinate*
;
Female
;
Humans
;
Papilloma*
;
Puberty
;
Skin Diseases
4.Milch osteotomy for the correction of cubitus valgus and cubitus varus deformities.
Sung Joon KIM ; Kuhn Sung WHANG ; Kyeong Jin CHOI ; Young Hwan KIM
The Journal of the Korean Orthopaedic Association 1993;28(3):1029-1036
No abstract available.
Congenital Abnormalities*
;
Osteotomy*
6.A Case of Acquired Tufted Angioma.
Jae Young HWANG ; Jin Woo PARK ; Sung Yul LEE ; Jong Suk LEE ; Kyu Uang WHANG
Korean Journal of Dermatology 1999;37(1):128-130
Acquired tufted angioma is a benign, progressive vascular lesion that has a distinctive histopathologic appearance. We report a 31-year-old man with acquireed tufted angioma. Several reddish papules and plaque were present on the neck. The lesion had been present for 6 months. They had enlarged slowly, and were slightly tender. Histopathologic examination of the biopsy specimen showed round to ovoid cellular tufts of capillaries, most prominent in the middle to lower dermis.
Adult
;
Biopsy
;
Capillaries
;
Dermis
;
Hemangioma*
;
Humans
;
Neck
7.Residual biliary stone removal using basket
Ki Whang KIM ; Sung Yee CHOO ; Sang Jin KIM ; Jong Tae LEE
Journal of the Korean Radiological Society 1984;20(4):734-739
Residual biliary stone can be effectively treated by nonoperative procedure using steerable catheter andbasket in the recent year. We analysed the 27 cases of residual biliary stone, which were refered to radiologydepartement of Yonsei University during last 2 years, from June 1982 to June 1984. The results as follows; 1. Thelocation of residual stones are extrahepatic in 14 cases (51.9%), intrahepatic in 5 cases(18.5%) and both intraand extrahepatic duct in 8 cases(29.6%). 2. In 13 of 27 cases(48.1%) were required multiple sessions. 3.Fragmentation of stone was done in 16(59.3%) in 27 cases. 4. Success rate in extrahepatic duct is 13 in 14casese(92.6%), intrahepatic duct 3 cases in 5(60%), and both intra and extrahepatic duct 7 in 8 cases(87.5%).Overal success rate in 27 cases is 85.2%
Catheters
8.A Clinical Study of Congenital Dislocation of the Hip
Jun Seop JAHNG ; Kuhn Sung WHANG ; In Hee CHUNG ; Jin Woong KIM
The Journal of the Korean Orthopaedic Association 1978;13(4):599-606
Congenital dislocations of the hip are all present at birth. Therefore if adequate examination of all newborn infants is done regularly, it should theoretically never be seen in adolescents or adults. Both the pathogenesis and management of congenital dislocation of the hip remain controversial topics. Closed reduction of simple congenital dislocations of the hip with retention in frog position was introduced by Lorenz. After this great efforts to receive these patients for treatment as early as possible were made by investigators. Also numerous surgical procedures and modifications have been used. Congenital dislocations of the hip were known to be uncommon in Korea. Nevertheless adolescents with untreated dislocations were not rarely met. The author studied congenital dislocation of the hip for sex incidence, X-ray findings, birth history, relation with combining anomaly and the results of treatment, In this study, 39 cases of congenital dislocation of the hip, treated at the Orthopedic Department of Severance Hospital during 7 years and 6 months from July, 1970 until December, 1977, were reviewed. The results of this study are as follows: 1. The annual number of the patients who were treated at Severance Hospital has not changed markedly. 2. The number of female patients was much greater than males. The ratio of female to male was 9 to 1. 3. The incidence of bilateral involvement was relatively low compared to the western coutries. 4. Congenital anomaly associated with congenital dislocation of hip occurred in about 7.8%. 5. The acetsbular index, C-E angle, Y-coordinate and height on affected hips are aggrevated according to the increment of age. 6. Closed reduction was satiafactory in 16 cases among 22 cases under the age of 3, but 4 cases were treated by operation. 7. Open reduction was performed in 8 cases, Salter's innominate osteotomy in 8 cases, Colonna's capsular arthroplasty in 2 cases, and supracondylar osteotomy in 2 cases.
Adolescent
;
Adult
;
Arthroplasty
;
Clinical Study
;
Dislocations
;
Female
;
Hip
;
Humans
;
Incidence
;
Infant, Newborn
;
Korea
;
Male
;
Orthopedics
;
Osteotomy
;
Parturition
;
Reproductive History
;
Research Personnel
9.Dysplastic Gangliocytoma of Cerebellum(Lhermitte-Duclos Disease): Relation to Cowden Disease.
Chan Young CHOI ; Keum Cheul WHANG ; Choong Jin WHANG ; Sung Hye PARK
Journal of Korean Neurosurgical Society 2003;33(5):514-516
We report a case of dysplastic gangliocytoma of the cerebellum(Lhermitte-Duclos disease) that can cause progressive mass effect in the posterior fossa. Cowden disease is a rare autosomal dominant disorder characterized by mucocutaneous hamartoma and high incidences of systemic malignancies. The patient had no mucocutaneous lesions indicating Cowden disease. With recent advances in molecular genetics, the association between Lhermitte-Duclos disease and Cowden disease has been recognized, it is considered that Cowden disease is a new phakomatosis. Recognition of this association has direct clinical relevance and long term follow up may lead to the early detection of malignancy.
Ganglioneuroma*
;
Hamartoma
;
Hamartoma Syndrome, Multiple*
;
Humans
;
Incidence
;
Molecular Biology
;
Neurocutaneous Syndromes
10.Immunohistochemical Expression of bcl-2 and PCNA in Acquired Melanocytic Nevi.
Tae Jin KIM ; Sung Yul LEE ; Jong Suk LEE ; Kyu Uang WHANG
Korean Journal of Dermatology 2002;40(11):1325-1330
BACKGROUND: The histogenesis of acquired melanocytic nevi is still a matter of debate. One considers that nevus cells originate from epidermal melanocytes and the other postulates that nevus cells are of both neural and melanocytic origin. OBJECTIVE: To clarify this controversy, investigation of the growth dynamics and tissue homeostasis of nevi is needed. METHODS: We compared expressions for PCNA and bcl-2 in 12 intradermal nevi and 8 compound nevi by immunohistochemical staining. RESULTS: The results are summarizid as follows: 1. bcl-2 : Both intradermal and compound nevi exhibited strong perinuclear and cytoplasmic staining. There was diminution of staining with progressive descent into the dermis. 2. PCNA : The mean rate of PCNA-positive nevus cells was higher in compound nevi than in intradermal nevi. CONCLUSION: The findings of our study shows considerable differences between intradermal nevi and compound nevi in expressions for PCNA and bcl-2.
Cytoplasm
;
Dermis
;
Homeostasis
;
Melanocytes
;
Nevus
;
Nevus, Intradermal
;
Nevus, Pigmented*
;
Proliferating Cell Nuclear Antigen*