1.A Case of Rotor Syndrome.
Chan Kyu KANG ; Joung Sun KANG ; Hyoung Woo LEE ; Moon Kwan CHUNG ; Bong Sup SHIM ; Hyun Woo LEE
Yeungnam University Journal of Medicine 1989;6(2):257-263
Rotor syndrome is a rare disease of hereditary hyperbilirubinemia transmitted with autosomal recessive trait. In general, Rotor syndrome shows direct hyperbilirubinemia and there has been several reports since Sons's report in 1966, in Korea. A 34-year-old female was admitted with the chief complaint of intermittent icteric sclera for 24 years. There was no family history of jaundice. Rotor syndrome was diagnosed by oral cholecystogram, BSP retention test, 99mTc-DISIDA scan, liver biopsy and electron microscopy study of liver biopsy specimen. We report this case with brief review of the literature.
Adult
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Biopsy
;
Female
;
Humans
;
Hyperbilirubinemia
;
Hyperbilirubinemia, Hereditary*
;
Jaundice
;
Korea
;
Liver
;
Microscopy, Electron
;
Rare Diseases
;
Sclera
;
Technetium Tc 99m Disofenin
2.Effect of Ascorbic Acid Against the Oxidative Stress-Induced Cellular Senescence in Trabecular Meshwork Cells.
Jae Woo KIM ; Sun Hee KANG ; Keun Woo LEE
Journal of the Korean Ophthalmological Society 2013;54(3):490-495
PURPOSE: To investigate the effect of L-ascorbic acid (LAA) on oxidative-stress-induced cellular senescence in trabecular meshwork (TM) cells. METHODS: Primarily cultured human TM cells were exposed to 0, 10, or 100 microM hydrogen peroxide for 7 days with or without co-exposure of LAA. Cellular survival and nitrite production were assessed with MTT and Griess assays, respectively. SA-beta-gal staining was performed to quantify cellular senescence. RESULTS: Hydrogen peroxide decreased cellular survival, accompanied by decreased nitric oxide (NO) production. These decreases of cellular survival and NO production were abolished by co-exposure of 100 microM LAA. Analysis of SA-beta-gal staining revealed that LAA inhibited hydrogen peroxide-induced cellular senescence by 6.8% (p < 0.05). CONCLUSIONS: LAA may have a protective effect against the oxidative-stress-induced cellular senescence in TM cells.
Aging
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Ascorbic Acid
;
Cell Aging
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Humans
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Hydrogen
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Hydrogen Peroxide
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Nitric Oxide
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Oxidative Stress
;
Trabecular Meshwork
3.Clinical Evaluation of Unilateral Open-Angle Glaucoma: A Two-Year Follow-Up Study
Jeoung Woo NAM ; Yeon Soo KANG ; Mi Sun SUNG ; Sang Woo PARK
Chonnam Medical Journal 2021;57(2):144-151
To evaluate the clinical characteristics of unilateral open-angle glaucoma, patients diagnosed with unilateral open-angle glaucoma from January 2017 to October 2018 were divided into primary open-angle glaucoma and normal-tension glaucoma groups according to the type of glaucoma diagnosed. The glaucoma and the contralateral eyes were compared, and the contralateral eye was analyzed for conversion to glaucoma and its risk factors were assessed during the 2-year follow-up period. Among 99 patients, 36 were diagnosed with primary open-angle glaucoma and 63 with normal-tension glaucoma. When comparing the glaucoma eye with the contralateral eye, the visual field mean deviation value (all p<0.001), peripapillary retinal nerve fiber layer thickness (all p<0.001), macular ganglion cell layer-inner plexiform layer thickness (p< 0.001, p=0.003), and optic nerve cup-disc ratio (p=0.005, p<0.001) were significantly different in both the primary open-angle glaucoma and normal-tension glaucoma groups. In normal-tension glaucoma, peripapillary retinal nerve fiber layer thickness was significantly thinner in the glaucoma conversion group than in the glaucoma non-conversion group (p=0.008). It was significantly associated with glaucoma conversion (odds ratio=0.97, p=0.023). In conclusion, in patients with unilateral open-angle glaucoma, the contralateral eye may develop glaucoma. In particular, if the peripapillary retinal nerve fiber layer thickness is decreased in normal-tension glaucoma, the possibility of glaucoma conversion is high; hence, careful examination is required.
4.Clinical Evaluation of Unilateral Open-Angle Glaucoma: A Two-Year Follow-Up Study
Jeoung Woo NAM ; Yeon Soo KANG ; Mi Sun SUNG ; Sang Woo PARK
Chonnam Medical Journal 2021;57(2):144-151
To evaluate the clinical characteristics of unilateral open-angle glaucoma, patients diagnosed with unilateral open-angle glaucoma from January 2017 to October 2018 were divided into primary open-angle glaucoma and normal-tension glaucoma groups according to the type of glaucoma diagnosed. The glaucoma and the contralateral eyes were compared, and the contralateral eye was analyzed for conversion to glaucoma and its risk factors were assessed during the 2-year follow-up period. Among 99 patients, 36 were diagnosed with primary open-angle glaucoma and 63 with normal-tension glaucoma. When comparing the glaucoma eye with the contralateral eye, the visual field mean deviation value (all p<0.001), peripapillary retinal nerve fiber layer thickness (all p<0.001), macular ganglion cell layer-inner plexiform layer thickness (p< 0.001, p=0.003), and optic nerve cup-disc ratio (p=0.005, p<0.001) were significantly different in both the primary open-angle glaucoma and normal-tension glaucoma groups. In normal-tension glaucoma, peripapillary retinal nerve fiber layer thickness was significantly thinner in the glaucoma conversion group than in the glaucoma non-conversion group (p=0.008). It was significantly associated with glaucoma conversion (odds ratio=0.97, p=0.023). In conclusion, in patients with unilateral open-angle glaucoma, the contralateral eye may develop glaucoma. In particular, if the peripapillary retinal nerve fiber layer thickness is decreased in normal-tension glaucoma, the possibility of glaucoma conversion is high; hence, careful examination is required.
5.Morphological studies on recombinant virus(recB-8) selected by coinfection of the baculoviruses bombyx mori and autographa californica nuclear palyhedrosis viruses.
Ji Hyun] PARK ; Soo Dong WOO ; Beom Seok PKR ; Kang Sun PYU ; Jai Myung YANG ; In Shik CHUNG ; Seok Kwon KANG
Journal of the Korean Society of Virology 1993;23(1):95-104
No abstract available.
Baculoviridae*
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Bombyx*
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Coinfection*
6.The Role of Tc-99m HMPAO Brain Perfusion SPECT in the Psychiatric Disability Evaluation of Patients with Chronic Traumatic Brain Injury.
Young SO ; Kang Wook LEE ; Sun Woo LEE ; Ick Sung GHI ; Chang June SONG
Korean Journal of Nuclear Medicine 2002;36(4):232-243
No abstract available.
Brain Injuries*
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Brain*
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Disability Evaluation*
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Humans
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Perfusion*
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Technetium Tc 99m Exametazime*
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Tomography, Emission-Computed, Single-Photon*
7.Flow Cytometric DNA Analysis of Prostate Adenocarcinoma :Correlation with histologic grade and DNA ploidy.
Hong Ki LEE ; Kwang Sun SUH ; Dae Young KANG ; Jong Woo PARK
Korean Journal of Pathology 1993;27(1):40-49
Nuclear DNA content of 32 cases of prostate adenocarcinoma diagnosed 1986-1991 was determined by flow cytometry, with the use of paraffin-embedded archival tissue. The present study was done to define the relationship between clinical stage, histopathological grade, and DNA ploidy. Aneuploidy was found in 10(31.3%) cases including 7 cases of near-tetraploidy. Among diploid tumors, 36.4% were localized disease(stage A and B), 13.6% were characterized by invasion outside the prostate(stage C), and 50.0% showed distant metastasis(stage D). Among aneuploid tumors, 10.0% were stage B, 50.0% stage C, and 40.0% stage D. The degree of glandular differentiation was characterized by the Gleason score and the percentage of sampled tissue involved by carcinoma was graded by Dhom's method. Apparent correlation was found between Gleason grade and Dhom grade(P<0.05). All 13 tumors with a Gleason grade I(score of 2 to 5) were diploid. Four of 9 tumors with a Gleason grade II(score of 6 to 7) were aneuploid(near-tetraploidy 33.3%, aneuploidy 11.1%) and 60.0%, of tumors with a Gleason grade III(score of 8 to 10) were aneuploid(near-tetraploidy 40.0%, aneuploidy 20%). The percentage of aneuploid cases increased with advanced clinical stage, but the relationship between aneuploidy versus clinical stage was not significant. However, it can be concluded that DNA ploidy correlates well with Gleason grade(p<0.05), which may have predictive prognostic value for prostate adeno-carcinomas.
Adenocarcinoma
8.Adrenergic Genetic Mechanisms in Hypertension and Hypertensive Kidney Disease.
Electrolytes & Blood Pressure 2013;11(1):24-28
Catecholamine secretory traits were significantly heritable, as were stress-induced blood pressure changes. Tyrosine hydroxylase (TH) is the rate-limiting enzyme in catecholamine biosynthesis. In the tyrosine hyroxylase promoter, significant associations were found for urinary catecholamine excretion and for blood pressure response to stress. TH promoter haplotype 2 (TGGG) showed pleiotropy, increasing both norepinephrine excretion and blood pressure during stress. In hypertension, 2 independent case-control studies (1,266 subjects with 53% women and 927 subjects with 24% women) replicated the effect of C-824T in the determination of blood pressure. Chromogranin A (CHGA) plays a fundamental role in the biogenesis of catecholamine secretory granules. Changes in the storage and release of CHGA in clinical and experimental hypertension prompted us to study whether genetic variation at the CHGA locus might contribute to alterations in autonomic function, and hence hypertension and its target organ consequences such as hypertensive kidney disease (nephrosclerosis). Systematic polymorphism discovery across the human CHGA locus revealed such regulatory regions as the proximal promoter and 3'-UTR. In chromaffin cell-transfected CHGA 3'-UTR and promoter/luciferase reporter plasmids, the functional consequences of the regulatory/non-coding allelic variants were documented. Variants in both the proximal promoter and the 3'-UTR displayed statistical associations with hypertension and hypertensive end stage renal disease. Therefore, I would like to review the common genetic variation in TH and CHGA as a cause of inter-individual variation in sympathetic activity, and ultimately blood pressure and hypertensive kidney disease.
Blood Pressure
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Case-Control Studies
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Chromogranin A
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Female
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Genetic Variation
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Genomics
;
Haplotypes
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Humans
;
Hypertension
;
Kidney
;
Kidney Diseases
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Kidney Failure, Chronic
;
Norepinephrine
;
Plasmids
;
Regulatory Sequences, Nucleic Acid
;
Secretory Vesicles
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Tyrosine
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Tyrosine 3-Monooxygenase
;
Organelle Biogenesis
9.A Case of Postirradiation Uterine Papillary Serous Carcinoma.
Jin Woo SHIN ; Eung Seok LEE ; In Sun KIM ; Jae Seong KANG
Korean Journal of Obstetrics and Gynecology 2000;43(6):1106-1108
Uterine papillary serous carcinoma is a morphologically distinct variant of endometrial carcinoma that is associated with an aggressive behavior with rapid progression and high recurrence, and poor response to salvage treatment. The most common type of malignancy developing in the uterus after radiation therapy is the malignant mixed mullerian tumor, however, the papillary serous carcinomas have rarely been reported.Here we report a case of uterine papillary serous carcinoma which had developed 7 years after radiation therapy for invasive cervical cancer.
Endometrial Neoplasms
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Female
;
Recurrence
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Uterine Cervical Neoplasms
;
Uterus
10.The Pathomorphologic Study of Spinal Stenosis as Seen on CT - Myelography of the Lumbar.
Woo Seog LEE ; Byung Gyu AHN ; Sun Kil CHOI ; Seung Koo KANG
Journal of Korean Neurosurgical Society 1987;16(2):439-446
This study has been examined different morphologic measurements in the evaluation of patients with lumbar spinal stenosis. Preoperative CT-Myelography from 30 patients who underwent surgery for central lumbar stenosis were analyzed. Based on this, we concluded as follows : 1) Bony measurement alone did not reliably identify patients with spinal stenosis. 2) Measurement of the transverse area of the dural sac on CT-Myelography was the most accurate method for identifying stenosis. 3) Lumbar myelography was still considered to have an important role in the valuation of a patient with stenosis because of correlation between the cross-sectional area of the dural sac and the anteroposterior diameter of the dural sac was excellent. 4) We identified soft-tissue problems as the main cause of stenosis. 5) The most common level of maximum stenosis was L4-5.
Constriction, Pathologic
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Humans
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Myelography*
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Spinal Stenosis*