1.Bone Marrow Cell Culture(GM-CFU) in Anaplastic Anemia of Children.
Journal of the Korean Pediatric Society 1985;28(9):888-898
No abstract available.
Anemia*
;
Bone Marrow Cells*
;
Bone Marrow*
;
Child*
;
Humans
2.Comparison of portal CT and indirect portography in hepatic masses.
Jung Kon KOH ; Jae Chang CHANG ; Bok Hwan PARK
Journal of the Korean Radiological Society 1993;29(2):255-261
We compared 87 portographic filling defects detected by portal CT in 64 patients were compared with those obtained by indirect portography. The indirect portography could visualize portogram only in anterior-posterior view. But the portal portal CT could visualize both portogram and hepatogram. We examined the portal CT and indirect portography and compared the accuracy of the both methods to evaluate the limitation and significance of the indirect protography. The mass shape lesions were seen on the portal CT which means portal flow defects of the mass lesions only could not depict totally in indirect portography (0%, 0/41). And the larger defects than real mass lesion were seen in portal CT means mass with associated portal flow defect and find portal vein invasion around the mass in 52% (24/46) of the indirect portography. Among them, only 66% of mass were detected correctly in the indirect portography comparing with mass lesion in portal CT. In summary, indirect portogram could not detect small filling defects which detected in portal CT and could not depict the extent of large filling defects. It also could not visualize correctly the protal flow in non-lesion side of the liver parenchyma.
Humans
;
Liver
;
Portal Vein
;
Portography*
3.Role of splints in microsurgical reversal of tubal sterilization.
Jung Gu KIM ; Jung Rae NOH ; Seok Kyun KIM ; Chang Jae SHIN ; Yoon Seok CHANG
Korean Journal of Obstetrics and Gynecology 1993;36(7):2161-2168
No abstract available.
Splints*
;
Sterilization, Tubal*
4.Expression of Proliferating Cell Nuclear Antigen and p53 Protein in Ovarian Epithelial Tumors.
Jong Jae JUNG ; Jong Hee NAHM ; Chang Soo PARK
Korean Journal of Pathology 1998;32(3):193-200
p53 gene mutation is commonly accepted to be associated with loss of negative cell cycle control and progression of tumors. The proliferative activity of tumor cells is considered to be a valuable indicator of tumor aggressiveness. This study is intended to compare p53 protein expression with cell proliferation rates in the ovarian epithelial tumors according to the various clinicopathological parameters. Immunohistochemistry using monoclonal p53 antibody (DO-1) and PCNA antibody (PC10) was applied to 56 cases of ovarian epithelial tumors including 17 cases of borderline tumor. The results were as follows. Both immunohistochemical staining of PCNA and p53 protein showed positive reactions confined to the nuclei of tumor cells. There were significant differences of p53 protein expression rates between borderline malignancies (11.8%) and cystadenocarcinomas (56.4%) of ovary. The expression rate of p53 protein was not significantly different according to the differentiation and the stage, but the cases of strong positive reaction to p53 protein were more frequently noted in the poorly differentiated and advanced staged tumors. The PCNA indices of p53 strong positive cases were higher than those of p53 weak positive cases. In summary, p53 protein and PCNA expression may be used as an adjuvant in differentiating borderline lesions from carcinomas of ovary and predicting their biological behaviors.
Cell Cycle Checkpoints
;
Cell Proliferation
;
Cystadenocarcinoma
;
Female
;
Genes, p53
;
Immunohistochemistry
;
Ovary
;
Proliferating Cell Nuclear Antigen*
5.Endodermal Sinus Tumor in Children.
Jae Sun JUNG ; Hyo Seop AHN ; Chang Yee HONG
Journal of the Korean Pediatric Society 1988;31(6):772-778
No abstract available.
Child*
;
Endoderm*
;
Endodermal Sinus Tumor*
;
Humans
6.Vascular Nature of Liver Abscess Examined with Computed Tomography: Separated Identification of the Four Layers and Difference According to the Various Factors of Abscess.
Jae Chun CHANG ; Hyun Cheol CHO ; Jung Kon KOH
Journal of the Korean Radiological Society 1994;31(2):321-326
PURPOSE: To identify the four layers based on intranodular vascular nature visible in multiphase incremental bolus dynamic CT and to determine any differential points according to various factors of liver abscess with this vascular nature or not. MATERIALS AND METHODS: We categonized 29 cases of confirmed liver abscess into three different groups according to presence of four layers visible in early phase(arterial phase) of CT. Three groups were compared in regard to the results of antiamebic antibody test and bacteriologic study and presense of cholangitic abscess and internal septation. RESULTS: We could separate four layers, innermost hypodense central cavitary lesion, hyperdense granular tissue, hypodense abscess wall and outermost hyperdense compensatory hypervascular zone in 18 cases(62%), only two layers, cavity and wall in six cases(21%), and characteristically we could find three layers without innermost cavitary lesion in five cases(17%). But we couldn't find significant correlations between various clinical factors of liver abscess and our vascular groups. CONCLUSION: Our method of CT could represent four layers based on vascularity in 62% of cases. And also could find the unusual inflammatory mass containing three layer which must be differentiated from other malignant solid mass. But we couldn't find differential point between various clinical factor of liver abscess and imaging diagnosis. We think that with the improvement of hardware such as spiral CT, identification of four layers will be earier and will be very helpful in early detection and proper treatment planning of liver abscess.
Abscess*
;
Diagnosis
;
Liver Abscess*
;
Liver*
;
Tomography, Spiral Computed
8.Tumor Angiogenesis in Renal Cell Carcinoma.
Ji Shin LEE ; Jong Jae JUNG ; Chang Soo PARK
Korean Journal of Pathology 1999;33(11):1055-1060
Angiogenesis is essential for the growth of solid tumors. Microvessel counts, which represent a measure of tumor angiogenesis, have been correlated with the overall survival of patients with a variety of malignancies. However, the significance of angiogenesis in renal cell carcinoma remains controversial. To determine whether angiogenesis correlates with prognosis of patients with renal cell carcinoma, we counted the microvessels within the primary tumors and compared their numbers with patients' prognosis. Tumor specimens from 42 patients were investigated. Microvessels were stained with anti-CD34 and anti-factor VIII-related antigen monoclonal antibodies. Significant correlation between microvessel counts for two antibodies was observed (r=0.875, p<0.01), although microvessel counts for CD34 were approximately two times higher. Microvessel counts were higher in clear cell than in non-clear cell carcinoma (p<0.05). These results suggest that immunostaining with anti-CD34 antibody may provide a more sensitive and accurate measure of tumor angiogenesis. There was no correlation between microvessel counts and nuclear grade, or TNM stage. In univariate analyses, nuclear grade and TNM stage were significantly associated with patient survival (p<0.01). But further studies on tumor angiogenesis of renal cell carcinoma are needed before it can be adopted as a prognostic marker.
Antibodies
;
Antibodies, Monoclonal
;
Carcinoma, Renal Cell*
;
Humans
;
Microvessels
;
Prognosis
;
von Willebrand Factor
9.Tumor Angiogenesis in Renal Cell Carcinoma.
Ji Shin LEE ; Jong Jae JUNG ; Chang Soo PARK
Korean Journal of Pathology 1999;33(11):1055-1060
Angiogenesis is essential for the growth of solid tumors. Microvessel counts, which represent a measure of tumor angiogenesis, have been correlated with the overall survival of patients with a variety of malignancies. However, the significance of angiogenesis in renal cell carcinoma remains controversial. To determine whether angiogenesis correlates with prognosis of patients with renal cell carcinoma, we counted the microvessels within the primary tumors and compared their numbers with patients' prognosis. Tumor specimens from 42 patients were investigated. Microvessels were stained with anti-CD34 and anti-factor VIII-related antigen monoclonal antibodies. Significant correlation between microvessel counts for two antibodies was observed (r=0.875, p<0.01), although microvessel counts for CD34 were approximately two times higher. Microvessel counts were higher in clear cell than in non-clear cell carcinoma (p<0.05). These results suggest that immunostaining with anti-CD34 antibody may provide a more sensitive and accurate measure of tumor angiogenesis. There was no correlation between microvessel counts and nuclear grade, or TNM stage. In univariate analyses, nuclear grade and TNM stage were significantly associated with patient survival (p<0.01). But further studies on tumor angiogenesis of renal cell carcinoma are needed before it can be adopted as a prognostic marker.
Antibodies
;
Antibodies, Monoclonal
;
Carcinoma, Renal Cell*
;
Humans
;
Microvessels
;
Prognosis
;
von Willebrand Factor
10.A case of Renal Vein Thorombosis Associated with Nephrotic Syndrome.
Kyung Hwa JUNG ; Woo Mok BYUN ; Jae Chun CHANG
Yeungnam University Journal of Medicine 1987;4(2):179-184
Renal vein thrombosis is usually a complication of multiple underlying renal disease rather than primary process. High incidence of renal vein thrombosis in patients with nephritic syndrome, which suggest the nephrotic syndrome play a paramount role in the genesis of renal vein thrombosis or thromboembolic phenomena. But these are likely to relationship of “egg and chicken”, and then we cannot determine what is primary of these. Recently authors experienced a case that was questioned renal vein thrombosis with nephrotic-syndrome clinically, laboratory and preliminary radiologically, and this case in confirmed by selective left renal venography. Here we report a case of renal vein thrombosis with nephrotic syndrome which successfully managed with oral anticoagulants and reviewed literatures.
Anticoagulants
;
Humans
;
Incidence
;
Nephrotic Syndrome*
;
Phlebography
;
Renal Veins*
;
Thrombosis