1.Immunohistochemical Study on Expression of Extracellular Matrix Components in Glomerular Diseases.
Korean Journal of Pathology 1994;28(3):288-296
Most glomerular lesions are associated with qualitative and quantitative alterations of the extracellular matrix components, having relation to progressive glomerular sclerosis. We aimed to investigate the characteristic alteraltions in distribution of extracellular matrix components, such as fibronectin, laminin, collagen type III and IV in human glomerular diseases by immunohistochemical method. The materials included are 3 nephrectomy as normal control, 51 renal biopsies and I autopsy; 3 normal, 5 minimal change disease, 5 minimal change disease with minimal mesangial lgA deposit, 5 benign recurrent hematuria, 10 focal segmental glomerulosclerosis, 15 lgA nephropathy, 10 membranoproliferative glomerulonephritis, 2 diffuse mesangial sclerosis of infancy. Type IV collagen and laminin were present normally in the mesangium, GBM, TBM and interstitial vessels, and were increased at the portion of increased mesangial matrix, of sclerosis and thickened GBM in cases of lgA nephropathy, membranoproliferative glomerulonephritis, focal segmental glomrulosclerosis and diffuse mesangial sclerosis in the proportion to the glomerular damage. Type III collagen was absent in the normal glomeruli, but was detectable focally and segmentally in cases of membranoproliferative glomerulonephritis, IgA nephropathy and focal segmental glomerulosclerosis at the sclerotic portion. Fibronectin was normally detectable mainly in the mesangium, and partly and incompletely in GBM, and was increased at the portion of increased mesangial matrix, sclerosis and thickened GBM in cases of focal segmental glomerulosclerosis, membranoproliferative glomerulonephritis, IgA nephropathy and diffuse mesangial sclerosis, but was diminshed at the old slcerotic portion or global sclerosis. The expression of these antibodies in cases of minimal change disease, minimal change disease with minimal mesangial IgA deposit, benign recurrent hematuria was not different, quantitatively and qualitatively, from that of normal glomeruli. These findings suggest that progressive glomerular sclerosis was due to the increase of extraceuular matrix components such as type IV collagen, laminin, fibronectin and new appearance of type III collagen, and the expression was in proportion to the degree of sclerosis, but had no relation to the disease entity.
Humans
;
Biopsy
2.Expression of ras Oncogene in Tumor Cells of Epidermis.
Sung Kyun KIM ; Kyu Chul CHOI ; Sun Wook HWANG
Korean Journal of Dermatology 1988;26(2):153-159
DNA isolated from human tumor cells can induce malignant transfarmation of tissue culture cells. The DNA is then called an oncogene. Its protein produets have been detected in animal and human tumors and are considered to play a significant role in carcinogenesis. In order to evaluate whether the oncogenes are involved in development of tumors of epidermis and whether they could be used as tumor markers, immunoperoxidase staining was performed for the ras product in sections of squamous cell carcinoma, Bowen's disease, actinic keratosis, keratoacanthoma and seborrheic keratosis. Three cases of sgamous cell carcinoma showed 10~20 positive cells per high power field(HPF). Three cases of Bowen's disease revealed 1-9 positive cells per HPF, whereas the actinic keratosis 1~9 or no positive cells per 10 HPF in all three cases. The keratoacanthoma and seborrheic keratosis showed 1~9 or no positive cells in all observed cases. The positive staining was observed in the cytoplasm. The increasing positivity in parallel with the increase of malignant potential strongly suggests that the ras oncogene is closely related to development of epidermal malignancy and also point out the possibility of ras as a cancer marker.
Animals
;
Bowen's Disease
;
Carcinogenesis
;
Carcinoma, Squamous Cell
;
Cytoplasm
;
DNA
;
Epidermis*
;
Genes, ras*
;
Humans
;
Keratoacanthoma
;
Keratosis, Actinic
;
Keratosis, Seborrheic
;
Oncogenes
;
Biomarkers, Tumor
3.Interstitial Mononuclear Cell Infiltration and its Phenotypes in IgA Nephropathy.
Hyeon Joo JEONG ; Hyunee YIM ; Sun Hee SUNG ; In Joon CHOI
Korean Journal of Pathology 1994;28(5):506-510
To know the correlation between glomerular and tubulointerstitial lesion and to define the characteristics of interstitial inflammatory cell in IgA nephropathy and classified according to WHO classification and graded tubulointerstitial lesion as mild, moderate and severe. Paraffin-embedded 5u sections were stained with UCHL-l, L26 and CD68 antibodies. More than 20 fields were examined in each case under the high power microscopy and the number of positive cells were counted. There was positive correlation between the severity of glomerular and that of tubulointerstitial lesion. The mostcommoninflammatory cells in the interstitiuin were UCHL-l positive cells followed by CD68 and L26 positive cells. As the WHO grade or tubulointerstitial lesion increased, the numbers of positive cells were increased in all three groups. The proportion of UCHL-1 Positive cells were increased in cases with high WHO grade whereas that of L26 positive cells incases with severe tubulointerstitial lesion Proteinuria was correlated with the degree of inflammatory cell infiltration, especially with that of L26 positive cells.
4.Muscular Hamartoma of the Breast: A case report.
Dong Won MIN ; Sun Hee SUNG ; In Joon CHOI
Korean Journal of Pathology 1994;28(1):86-89
Hamartoma of the breast is relatively rare benign tumor, which is a well-circumscribed mass mainly composed of fibrous stroma, a(tipose tissue, ducts and acini. Muscular hamartoma of the breast is mainly composed of smooth muscle, and is extremely rare because proper smooth muscle is normaly absent in the breast except in the nipple. We describe a rare case of muscular hamartoma of the breast in a 38-year-old woman. This tumor was located in the upper outer quadrant and a 3 x 2.5 x 2 cm sized, well-demarcated but not encapsulated mass, The mass consisted mainly of irregularly arranged smooth muscle bundles in the fibrous stroma with lobular units and admixed fat cells. The origin of smooth muscle in hamartoma is not well known.
Female
;
Humans
;
Hamartoma
5.Irritated Seborrheic Keratosis: Report of two Cases.
Kyu Cherl CHOI ; Sung Kyun KIM ; Sun Wook HWANG
Korean Journal of Dermatology 1982;20(4):551-555
No abstract available.
Keratosis, Seborrheic*
6.Aggressive AngiOmYxoma Occuring in Ischiorectal Fossa: A case report.
Jai Hyang GO ; Sun Hee SUNG ; In Joon CHOI
Korean Journal of Pathology 1994;28(1):99-101
We report a case of aggressive angiomyxoma in ischiorectal fossa of a 39-year-old women. The tumor is characterized by relatively large size(13 x 11 cm), grossly gelatinous appearance and locally infiltrative nature. Microscopically, it consists of many variable sized blood vessels and spindle or stellate cells widely separated in myxoid or collagenous stroma. Immunohistochemical stains reveal that the tumor cells are strongly positive for actin and desmin. Electron microscopic findings are that of a few cells dispersed in abundant intercellular substance and collagen bundles. These cells form irregular cytoplasmic process without basal lamina and contain endoplasmic reticulum having cistern.
Female
;
Humans
7.STUDY OF SATISFACTION OF NASAL BONE REDUCTION IN ARMY.
Sun Shik SHIN ; Sung Ho KIM ; Kwang Shik KOOK ; Sung Ho CHOI ; Kyung Tae BAE
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1997;24(6):1352-1357
No abstract available.
Nasal Bone*
8.A Case of Surgically Corrected-Combined form of Total Anomalous Pulmonary Venous Return.
Dae Sung HWANG ; Sun Hwan CHO ; Jong Bum CHOI ; Hyang Suk YOON ; Soon Ho CHOI
Korean Circulation Journal 1992;22(3):473-478
Total anomalous pulmonary venous return(connection) is a congenital heart disease. Especially, the reports of the patients with double connections of all pulmonary veins were rare. An infant who underwent operation for total anomalous pulmonary venous return had double drainge of all pulmonary veins to both left vertical vein and anomalous descending vein. This second lesion was not diagnosed preoperatively, but in operative field. Operative treatments were performed by ligation of left vertical vein and central pulmonary vein-to-left atrium anastomosis without ligation of the descending anomalous vein. For these less common variants fo total anomalous pulmonary venous return,a more detailed and precise understanding of morphology can facilitate accurate surgical repair. And also, early detection of the disease is an another issue for a good prognosis.
Heart Defects, Congenital
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Humans
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Infant
;
Ligation
;
Prognosis
;
Pulmonary Veins
;
Scimitar Syndrome*
;
Veins
9.A clinicopathologic study of first branchial cleft anomaly.
Sung Won CHAE ; Geon CHOI ; Chung Sik CHOI ; Sun Jae HWANG
Korean Journal of Otolaryngology - Head and Neck Surgery 1993;36(2):258-263
No abstract available.
Branchial Region*
10.A Case of Colonoscopically Removed Granular Cell Tumor in the Ascending Colon.
Jae Kyung CHOI ; Myoung Gyu CHOI ; Kyu Yong CHOI ; In Sik CHUNG ; Sang Bok CHA ; Kyu Won CHUNG ; Hee Sik SUN ; Boo Sung KIM ; Young Jin CHOI ; An Hee LEE
Korean Journal of Gastrointestinal Endoscopy 1991;11(2):383-386
This case report describes a patient with semipedunclated granuylar cell tumor(granular cell myoblastoma) of the proximal ascending colon removed by endoscopic polypectomy. A 39-year old femalie was visited to our hospital for intermittent abdominal pain and loose stool. Colonoscopic examination showed a semipedunclated lesion covered with yellowish white smooth mucosa in the proximal ascending colon. The tumor was removed by endoscopic polypectomy. The collected specimen was 0.9x0.8 cm in size. The cut surface of the specimen showed a white round firm tumor covered with mormal epithelium of the colon. Using immunohistochemical study, the tumor cells were to be positively stained by S-100 protein and negatively stained by desmin, which supports the concept of the Schwann cell origin of granular cell tumor. In Korea, 2 cases of granular cell tumor of the colon and rectum, which were treated by surgical removal, have been reported. This case in the first endoscopic polypectomy of granular cell tumor of the colon and retum in Korea. The endoscopic polypectomy is thought to be useful for the therapy of small pedunclated or semipedunclated granular cell tumor, intracolonic type.
Abdominal Pain
;
Adult
;
Colon
;
Colon, Ascending*
;
Desmin
;
Epithelium
;
Granular Cell Tumor*
;
Humans
;
Korea
;
Mucous Membrane
;
Rectum
;
S100 Proteins