1.Clinical review of 874 patients with gastric cancer.
Young Jin KIM ; Suk Jin HONG ; Shin Kon KIM ; Young Kook CHO
Journal of the Korean Surgical Society 1993;45(6):937-945
No abstract available.
Humans
;
Stomach Neoplasms*
2.The trends of adolescent psychiatric researches in Korea.
Young Jin KOO ; Jae Woo LEE ; Kil Hong LEE
Journal of Korean Neuropsychiatric Association 1991;30(6):1111-1120
No abstract available.
Adolescent*
;
Humans
;
Korea*
3.Clinical trial with intraperitoneal hyperthermic perfusion for intraabdominal cancer with peritoneal metastasis.
Jin Young KIM ; Soung Kee HONG ; Jong Ha SON
Journal of the Korean Surgical Society 1992;42(2):199-205
No abstract available.
Neoplasm Metastasis*
;
Perfusion*
4.Edwards Syndrome: an autopsy case.
So Young JIN ; Woo Hee JUNG ; Chang Ho HONG
Korean Journal of Pathology 1986;20(3):343-348
Edwards syndrome is first introduced by Edwards and characterized by facial anomalies, multiple cardiovascular, gastrointestinal, urogenital, and skeletal malformations. It results from triplication of part or all of chromosome 18 in some or all of the patient's cells. It has an incidence of 1 in 4,500 live births or less and short life expectancy. Recently we experienced a case of 3-day-old female new born infant with this syndrome. Post mortem examination showed progeric face with prominent occiput, large flabby ears, microphthalmia, and micrognathia, bilateral clenched hands with flexion contraction of middle fingers, and bilateral rockerbottom feet. Internal examination revealed horseshoe kidney, esophageal atresia with tracheoesophageal fistula, two accessory spleens, and multiple cardiac anomalies. A trisomy 18 was confirmed by the cytogenetic study.
Infant
;
Male
;
Female
;
Infant, Newborn
;
Humans
;
Incidence
5.A Cse of Partial Trisomy 10q Syndrome.
Yong Chan PARK ; Ahn Hong CHOI ; Jin Young HAN
Korean Journal of Perinatology 1998;9(4):421-424
Partial trisomy 10q syndrome is a rare chromosome anomaly characterized by severe mental and growth retardation, craniofacial dysmorphia with prominent forehead, fine arched eyebrows, deep set small eyes and micrognathia, In addition, other physical manifestations have been reported as skeletal anomaly, congenital heart disease, inguinal hernia, and so on. We report a case of partial trisomy 10q syndrorne with certain stigmata which confirmed by chromosome analysis.
Christianity
;
Eyebrows
;
Forehead
;
Heart Defects, Congenital
;
Hernia, Inguinal
;
Trisomy*
6.A Case of Pityriasis Lichenoide Chronica Associated with Pseudoacanthosis Nigricans.
Jin Kwon KIM ; Young Hee HWANG ; Hong Il KOOK
Korean Journal of Dermatology 1982;20(3):437-441
Pityriasis lichenoides chronica is considered to be a benign disease. Erythematous yelIowieh scaly maeulea appear insidiously, chiefly on the sides of trunk, thighs and upper arms. Acanthosis nigricans is a rare cutaneous disorder with peak incidence in puberty characterized by hyperkeratosis and, dark pigmentation. We report a case of pityriasis lichenoides chronica assaciated with pseudoacanthosis nigricans in a 14 year-old obeae male patient who has bean sized erythematoua scaly papules on the trunk and extremities, velvety black brownish colored patchea on the neck and both axillary regions.
Acanthosis Nigricans
;
Adolescent
;
Arm
;
Extremities
;
Humans
;
Incidence
;
Male
;
Neck
;
Pigmentation
;
Pityriasis Lichenoides
;
Pityriasis*
;
Puberty
;
Thigh
7.Nesidioblastosis of the Pancreas.
Young Bae KIM ; Jin Sook JEONG ; Ahn Hong CHOI
Korean Journal of Pathology 1992;26(5):484-489
The morphologic abnormalities of the endocrine pancreas that underlie persistent neonatal hyperinsulinemic hypoglycemia and are included under the heading "nesidioblastosis" appears to be heterogeneous. This characteristic morphologic finding is ductuloinsular complexes showing endocrine cells budding off the ductoepithelium and merging with adjacent endocrine cell clusters. A case of nesidioblastosis associated with hyperinsulinemic hypoglycemia occurred in a 6/365 year-old male neonate. Microscopic finding of near totally resected pancreas revealed irregular sized islets and ductuloinsular complexes, both of which contained hypertrophied B cells with a few mitosis. Because of persistent hypoglycemia after first operation, he received second operation 8 days after. This histologic finding was more severe comparative to that of first operation. According to these findings, the pathogenesis of nesidioblastosis may be congenital or developmental defect of a kind of compensatory mechanism by unknown stimuli to acquire persistent hypoglycemia.
Male
;
Infant, Newborn
;
Humans
8.Determination of High Density Lipoprotein Cholesterol in Psoriasis Patients.
Joon Young SONG ; Kyu Suk LEE ; Jin Pyo HONG
Korean Journal of Dermatology 1986;24(4):493-498
In orper to measure the levels of high density lipoprotein cholesterol in psoriasis, 60 psoriatic patients and 30 healthy subjects were included in this study. Lopez-Virells methos was applied for measuring the serum level of high density lipoprotein cholesterol. The results were obtained as follows. The level of serurn HDL cholesterol was 58. 39+17. 40 mg/dl in psoratcs and 50.3+0.31 mg/dl in healthy subjects and 50. 43+ 10. 31 mg/dl in healthy subjects. No significant differences were noted between psoriatics & healthy subjects. 2. The level of serum HDL cholesterol was 56. 40+19. 10 mg/dl in male group of psoriatics and 60. 00+15.47 mg/dl in female group of psoriatics and 48.3+9. 50 mg/dl in healthy male group and 52.60 -10.59 mg/dl in healthy female group. No significant differences of serum HDL cholesteol levels were noted in both sexes.3. The mean value of serum HDL cholesterol by age groups of 10, 20, 30, 40, and 50 years old with psoriasis were 50. 70 mg/dl, 61. 97 mg/dl, 57. 44 mg/dl, 49. 11 mg/dl and 70. 36 mg/dl, respectively and those of healthy groups were 57. 25 mg/ dl, 45. 17 rng/dl, 50. 97 rng/dl, 48. 07 mg/dl and 46. 98 mg/dl, respectively.
Cholesterol, HDL*
;
Female
;
Humans
;
Male
;
Middle Aged
;
Psoriasis*
9.Transplantation of Cultured Keratinocytes in Autologous Fibrin Glue Suspension.
Jin Young KIM ; Sung Pyo HONG ; Jae Kyung PARK
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1999;26(4):531-537
The use of a cultured autologous keratinocyte sheet has become a recognized method for the coverage of extensive bums during recent years. The disadvantages of these sheet grafts are a long time-lag until keratinocyte sheets are available, the fragility and difficulty in handling of grafts, an unpredictable take rate and extremely high costs. In this study we investigated the transplantation of cultured keratinocytes as single cells suspended in autologous fibrin glue. In a rat model with standardized full thickness wounds, this new transplantation technique was evaluated and compared directly to the conventional keratinocyte sheet grafting technique. After transplantation, wounds were evaluated for the degree of epithelial coverage, and then microscopic structures were evaluated under light and electron microscopy. The results were as follows: 1) The fibrinogen solution prepared from autologous blood had 12 times more fibrinogen compared to the original blood. 2) After transplantation of cultured keratinocyt-es in fibrin glue, the degree of epithelial coverage was 79% at 2 weeks, which was comparable to 17% for cultured keratinocyte sheet graft 3) Typical basement membrane structures were consistently found at 2 weeks after transplantation of keratinocytes in fibrin glue. 4) Rete ridges were found at 4 weeks after transplantation of keratinocytes in fibrin glue. In conclusion, the transplantation technique of keratinocytes in fibrin glue is available earlier than sheet grafts, it transfers actively proliferating cells and it simplifies the grafting procedure. As well, this technique leads to an earlier epithelial covering and an earlier restoration of the dermo-epidermal junction than sheet grafting.
Basement Membrane
;
Fibrin Tissue Adhesive*
;
Fibrin*
;
Fibrinogen
;
Keratinocytes*
;
Microscopy, Electron
;
Models, Animal
;
Transplants
;
Wounds and Injuries
10.Analysis of DNA ploidy patterns of anal condyloma acuminata: correlation with anal cancer.
Young Jin KIM ; Woon Ki HONG ; C Juan FELIX
Journal of the Korean Society of Coloproctology 1993;9(2):131-134
No abstract available.
Anus Neoplasms*
;
DNA*
;
Ploidies*