1.The Roles of IgG and Albumin as a Predictor of Frequent Relapse in Nephrotic Syndrome.
Journal of the Korean Pediatric Society 1994;37(9):1245-1250
The etiology of nephrotic syndrome in unknown. The characterization were proteinuria, hypoalbuminemia, generalized edema and hyperlipidemia. To assess the recurrence factors in the nephrotic syncrome, we measured serum immunoglobulin (IgG, IgA, IgM), albumin, complement, cholesterol and the 24-hour total urine protein at the initial relapse of nephrotic syndrome. Each data of frequent and infrequent relapsed nephrotic syndrome were compared. In total 67 cases, 18 cases were frequent relapsers and 26 cases were infrequent relapsers and 23 cases were normal control without renal disease. The levels of IgG and albumin in frequent relapser were 304 mg/dl and 1.59 g/dl as compared with 440 mg/dl and 2.06 g/dl in infrequent relapsers. The levels of IgG and albumin were signifecantly lower in frequent relapser than infrequent relapsers (p<0.05). This study might be useful to predict that very low levels of IgG and albumin at the first relapse might be related to high risk chances of frequent relapse in children with nephorotic syncrome.
Child
;
Cholesterol
;
Complement System Proteins
;
Edema
;
Humans
;
Hyperlipidemias
;
Hypoalbuminemia
;
Immunoglobulin A
;
Immunoglobulin G*
;
Immunoglobulins
;
Nephrotic Syndrome*
;
Proteinuria
;
Recurrence*
4.A Case of Multicystic Renal Dysplasia with Chromosomal Abnormality.
Myung Jae LEE ; Soon In JUNG ; Jae Hyung NA ; Jae Hong KIM ; Jong Jae JUNG
Korean Journal of Perinatology 1999;10(1):56-60
Holoprosencephaly is a rare and complex malformation affecting the cleavage of the developing forebrain and is usually associated with defects of the mid Face. We have experienced a case of holoprosencephaly, diagnosed prenatally by ultrasound examination at 31 weeks of pregnancy in a 31-year-old primigravida woman. This case is characterized by holoprosencephaly, cleft palate, cleft lip, left renal aplasia and right renal hypertrophy. The chromosomal study showed a deletion of the long arm of chromosome 7, 46, XX, del(7)(q32), We report with a terminal deletion of chromosome 7q associated with atypical clinical picture and holoprosencephaly.
Adult
;
Arm
;
Chromosome Aberrations*
;
Chromosomes, Human, Pair 7
;
Cleft Lip
;
Cleft Palate
;
Female
;
Holoprosencephaly
;
Humans
;
Hypertrophy
;
Multicystic Dysplastic Kidney*
;
Pregnancy
;
Prosencephalon
;
Ultrasonography
5.Pregnancy following intra-tubal insemination in a woman who ovulated prior to gamete intra-fallopian transfer(GIFT).
Sang Bok LEE ; Jung Soon PARK ; Jae Seung LEE ; Seung Jae LEE ; Jong Min PARK
Korean Journal of Obstetrics and Gynecology 1991;34(5):747-749
No abstract available.
Female
;
Humans
;
Insemination*
;
Pregnancy*
6.Acute Hydrogen Sulfide Poisoning: TWO CASES REPORT.
Jong Goo KIM ; Kyung Jong LEE ; Se Wi LEE ; Jae Beom PARK
Korean Journal of Occupational and Environmental Medicine 2000;12(1):148-155
Hydrogen sulfide poisoning is frequently encountered in the workplace. Two workers lost their consciousness in an underground tank at a factory producing paper. The tank contained liquid mixture of used paper, sodium oxygenate chloride(NaOC1), and sodium thiosulfate pentahydrate(NaSO3 5H90). A worker(worker A; 36-year-old man) entered tank to remove sludge. When worker A lost his consciousness, worker B entered the tank to rescue worker A, however he lost consciousness inside the tank. We discuss in detail the clinical features of this condition. Hydrogen sulfide poisonings have occurred in industries involving petroleum refining, the manufacture of heavy water, tanning of hides, vulcanization of rubber, and the manufacture of rayon. And it is necessary to stress the health education for workers and managers in these industries.
Adult
;
Consciousness
;
Deuterium Oxide
;
Health Education
;
Humans
;
Hydrogen Sulfide*
;
Hydrogen*
;
Oxygen
;
Petroleum
;
Poisoning*
;
Rescue Work
;
Rubber
;
Sewage
;
Sodium
;
Tanning
;
Triacetoneamine-N-Oxyl
7.A Study on the Expression of p53 Oncogene Products, PCNA Index and DNA Ploidy in Renal Cell Carcinoma.
Jong Jae JUNG ; Ji Shin LEE ; Chan CHOI
Korean Journal of Pathology 1997;31(7):672-682
Mutant p53 is associated with the advanced stages of some human tumor but there is a wide variation in the reported incidence of p53 mutation in renal cell carcinoma and its prognostic significances. We designed this study to assess the expression of p53 in renal cell carcinomas and to compare with the established prognostic factors. Immunoreactivity for p53 protein and proliferating cell nuclear antigen (PCNA) were assessed in 44 cases of primary renal cell carcinoma, and flow cytometric analysis of DNA ploidy was perfon-ned in 37 of those cases. p53 protein was over-expressed in 16/44 (36.4%) renal cell carcinomas and 5 rumors had more than 10 immunoreactive tumor cells. The expression of p53 protein was positively related to nuclear grade (p=0.007) and PCNA index (p=0.002), but was independent of stage and DNA ploidy. In univariate survival analysis, stage (p<0.001), nuclear grade (p=0.017), DNA ploidy (p=0.045) and PCNA index (p<0.001) were significantly associated with patient survival. However, considering the stage, all of the last three factors had no prognostic influence. Cases showing strong positivity of p53 expression had worse prognosis than those with no or weak p53 expression, especially in early lesions (stage I,II) (p<0.001).
Carcinoma, Renal Cell*
;
DNA*
;
Humans
;
Incidence
;
Oncogene Proteins*
;
Oncogenes*
;
Ploidies*
;
Prognosis
;
Proliferating Cell Nuclear Antigen*
8.Early and Late Complications of Radical Retropublic Prostatectomy.
Jae Won LEE ; Choung Soo KIM ; Han Jong AHN
Korean Journal of Urology 2000;41(11):1409-1414
No abstract available.
Prostatectomy*
9.The Clinical Coures of Mild Neonatal Hydronephrosis.
Jong Ho PARK ; Young Tae LEE ; Jae Seop SHIN
Korean Journal of Urology 2000;41(7):872-877
No abstract available.
Hydronephrosis*
10.Full-thickness skin grafts for vaginal reconstruction in mayer-fokitansky-hauser syndrom.
Jong Moon LEE ; Jae Sik HAN ; Won Kyun JUNG
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1998;25(5):897-901
Mayer-Rokitansky-Kuster-Hauser Syndrom is characterized by the absence of the vagina and the uterus, the presence of apparently normal tubes and ovaries, feminine appearance, normal female secondary sexual characteristics, a normal 46, XX karyotypes, and a feminine psychosexual orientation. Absence of the vagina results from an embryological arrest in the development of the lower portion of the Mullerian system. Various methods of surgical treatment for the vaginal absence in this syndrom have been introduced but the ideal method to restore the original dimension and function of the normal vagina was not found. The two cases reviewed in this paper were all treated with modified McIndoe operation using full thickness skin grafts. Postoperatively both women were satisfied without complications, i,e. lack of skin graft, bleeding, urethrovaginal fistula, perforation of the rectum, rectovaginal fistula and significant vaginal stricture. This paper reveals the satisfactory results that were uniformly good.
Constriction, Pathologic
;
Female
;
Fistula
;
Hemorrhage
;
Humans
;
Karyotype
;
Ovary
;
Rectovaginal Fistula
;
Rectum
;
Skin*
;
Transplants*
;
Uterus
;
Vagina