1.Successful Treatment of a Gastric Plasmacytoma Using a Combination of Endoscopic Submucosal Dissection and Oral Thalidomide.
Se Young PARK ; Hee Seok MOON ; Jae Kyu SEONG ; Hyun Yong JEONG ; Beum Yong YOON ; Se Woong HWANG ; Kyu Sang SONG
Clinical Endoscopy 2014;47(6):564-567
		                        		
		                        			
		                        			We report a rare case of a gastric plasmacytoma treated with endoscopic resection and oral thalidomide therapy. A 70-year-old man was admitted to our hospital with indigestion. He had no specific medical history and unremarkable laboratory results. Gastroendoscopic findings revealed a focal, erythematous, flat elevated lesion in the anterior wall of the stomach antrum. A biopsy revealed atypical lymphocytes. Endoscopic submucosal dissection (ESD) with an insulation-tipped knife was performed 45 days after diagnosis. Radiological and hematological evaluations, including a bone marrow biopsy, were performed and showed no involvement of other organs. The patient was diagnosed with extramedullary gastric plasmacytoma. Follow-up gastroendoscopy was performed three times during a 2-year period and showed nonspecific ESD scarring. The patient's condition was found to be stable.
		                        		
		                        		
		                        		
		                        			Aged
		                        			;
		                        		
		                        			Biopsy
		                        			;
		                        		
		                        			Bone Marrow
		                        			;
		                        		
		                        			Cicatrix
		                        			;
		                        		
		                        			Diagnosis
		                        			;
		                        		
		                        			Dyspepsia
		                        			;
		                        		
		                        			Follow-Up Studies
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Lymphocytes
		                        			;
		                        		
		                        			Plasmacytoma*
		                        			;
		                        		
		                        			Stomach
		                        			;
		                        		
		                        			Thalidomide*
		                        			
		                        		
		                        	
2.Characterization of allergic response induced by repeated dermal exposure of IL-4/Luc/CNS-1 transgenic mice to low dose formaldehyde.
Moon Hwa KWAK ; Ji Eun KIM ; Jun GO ; Eun Kyoung KOH ; Sung Hwa SONG ; Ji Eun SUNG ; Seung Yun YANG ; Beum Soo AN ; Young Jin JUNG ; Jae Ho LEE ; Yong LIM ; Dae Youn HWANG
Laboratory Animal Research 2014;30(3):95-103
		                        		
		                        			
		                        			Although formaldehyde (FA) is known to be a major allergen responsible for allergic contact dermatitis, there are conflicting reports regarding correlation between FA exposure and interleukin (IL-4) expression. To investigate whether allergic responses including IL-4 expression were induced by repeated dermal exposure to low dose FA, alterations in the luciferase signal and allergic phenotypes were measured in IL-4/Luc/CNS-1 transgenic (Tg) mice containing luciferase cDNA under control of the IL-4 promoter after exposure to 4% FA for 2 weeks. High levels of luciferase were detected in the abdominal region of the whole body and submandibular lymph node (SLN) of FA treated mice. Additionally, the ear thickness and IgE concentration were significantly upregulated in the FA treated group when compared with the acetone olive oil (AOO) treated group. FA treated mice showed enhanced auricular lymph node (ALN) weight, epidermis and dermis thickness, and infiltration of inflammatory cells. Furthermore, the expression of IL-6 among T helper 2 cytokines was higher in the FA treated group than the AOO treated group, while vascular endothelial growth factor (VEGF) levels remained constant. Overall, the results presented herein provide additional evidence that various allergic responses may be successfully induced in IL-4/Luc/CNS-1 Tg mice after exposure to low dose FA for 2 weeks. The luciferase signal under the IL-4 promoter may reflect general indicators of the allergic response induced by exposure to low dose FA.
		                        		
		                        		
		                        		
		                        			Acetone
		                        			;
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Cytokines
		                        			;
		                        		
		                        			Dermatitis, Allergic Contact
		                        			;
		                        		
		                        			Dermis
		                        			;
		                        		
		                        			DNA, Complementary
		                        			;
		                        		
		                        			Ear
		                        			;
		                        		
		                        			Epidermis
		                        			;
		                        		
		                        			Formaldehyde*
		                        			;
		                        		
		                        			Immunoglobulin E
		                        			;
		                        		
		                        			Interleukin-4
		                        			;
		                        		
		                        			Interleukin-6
		                        			;
		                        		
		                        			Interleukins
		                        			;
		                        		
		                        			Luciferases
		                        			;
		                        		
		                        			Lymph Nodes
		                        			;
		                        		
		                        			Mice
		                        			;
		                        		
		                        			Mice, Transgenic*
		                        			;
		                        		
		                        			Olea
		                        			;
		                        		
		                        			Phenotype
		                        			;
		                        		
		                        			Vascular Endothelial Growth Factor A
		                        			;
		                        		
		                        			Olive Oil
		                        			
		                        		
		                        	
3.Simvastatin inhibits osteoclast differentiation by scavenging reactive oxygen species.
Ho Jin MOON ; Sung Eun KIM ; Young Pil YUN ; Yu Shik HWANG ; Jae Beum BANG ; Jae Hong PARK ; Il Keun KWON
Experimental & Molecular Medicine 2011;43(11):605-612
		                        		
		                        			
		                        			Osteoclasts, together with osteoblasts, control the amount of bone tissue and regulate bone remodeling. Osteoclast differentiation is an important factor related to the pathogenesis of bone-loss related diseases. Reactive oxygen species (ROS) acts as a signal mediator in osteoclast differentiation. Simvastatin, which inhibits 3-hydroxy-3-methylglutaryl coenzyme A, is a hypolipidemic drug which is known to affect bone metabolism and suppresses osteoclastogenesis induced by receptor activator of nuclear factor-kappaB ligand (RANKL). In this study, we analyzed whether simvastatin can inhibit RANKL-induced osteoclastogenesis through suppression of the subsequently formed ROS and investigated whether simvastatin can inhibit H2O2-induced signaling pathways in osteoclast differentiation. We found that simvastatin decreased expression of tartrate-resistant acid phosphatase (TRAP), a genetic marker of osteoclast differentiation, and inhibited intracellular ROS generation in RAW 264.7 cell lines. ROS generation activated NF-kappaB, protein kinases B (AKT), mitogen-activated protein kinases signaling pathways such as c-JUN N-terminal kinases, p38 MAP kinases as well as extracellular signal-regulated kinase. Simvastatin was found to suppress these H2O2-induced signaling pathways in osteoclastogenesis. Together, these results indicate that simvastatin acts as an osteoclastogenesis inhibitor through suppression of ROS-mediated signaling pathways. This indicates that simvastatin has potential usefulness for osteoporosis and pathological bone resorption.
		                        		
		                        		
		                        		
		                        			Acid Phosphatase/genetics/metabolism
		                        			;
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Anticholesteremic Agents/*pharmacology
		                        			;
		                        		
		                        			Blotting, Western
		                        			;
		                        		
		                        			*Cell Differentiation
		                        			;
		                        		
		                        			Cells, Cultured
		                        			;
		                        		
		                        			Hydrogen Peroxide/pharmacology
		                        			;
		                        		
		                        			Isoenzymes/genetics/metabolism
		                        			;
		                        		
		                        			Macrophages/cytology/drug effects/metabolism
		                        			;
		                        		
		                        			Mice
		                        			;
		                        		
		                        			Mitogen-Activated Protein Kinases/genetics/metabolism
		                        			;
		                        		
		                        			NF-kappa B/genetics/metabolism
		                        			;
		                        		
		                        			Osteoclasts/*cytology/*drug effects/metabolism
		                        			;
		                        		
		                        			RANK Ligand/metabolism
		                        			;
		                        		
		                        			RNA, Messenger/genetics
		                        			;
		                        		
		                        			Reactive Oxygen Species/*metabolism
		                        			;
		                        		
		                        			Real-Time Polymerase Chain Reaction
		                        			;
		                        		
		                        			Simvastatin/*pharmacology
		                        			
		                        		
		                        	
4.Effect of Prostate Biopsy Hemorrhage on MRDW and MRS Imaging.
Jong Yeon LEE ; In Ho CHANG ; Young Tae MOON ; Kyung Do KIM ; Soon Chul MYUNG ; Tae Hyoung KIM ; Jong Beum LEE
Korean Journal of Urology 2011;52(10):674-680
		                        		
		                        			
		                        			PURPOSE: To retrospectively evaluate the effect of post-prostate-biopsy hemorrhage on the interpretation of magnetic resonance diffusion-weighted (MRDW) and magnetic resonance spectroscopic (MRS) imaging in the detection of prostate cancer. We also investigated the optimal timing for magnetic resonance examination after prostate biopsy. MATERIALS AND METHODS: We reviewed the records of 135 men. All patients underwent prostate magnetic resonance imaging (MRI). The prostate was divided into eight regions according to the biopsy site. Subsequently, we measured hemorrhage on apparent diffusion coefficient (ADC) values and (choline+creatinine)/citrate ([Cho+Cr]/Cit) ratios in the same regions on the MRI. We investigated the effect of hemorrhage at ADC values and (Cho+Cr)/Cit ratios on MRI and the relationship between prostate biopsy results and MRI findings. RESULTS: The mean patient age was 68.7 years and the mean time between biopsy and MRI was 23.5 days. The total hemorrhagic score demonstrated no significant associations with intervals from biopsy to MRI. Higher hemorrhagic scores were associated with higher ADC values, prostate cancer, and noncancer groups, respectively (p<0.001). ADC values were lower in tumors than in normal tissue (p<0.001), and ADC values were inversely correlated with tumor Gleason score in biopsy cores (p<0.001). However, (Cho+Cr)/Cit ratios did not exhibit any association with prostate biopsy results and hemorrhage. CONCLUSIONS: Hemorrhage had no significant associations with the interval from biopsy to MRI. ADC values may help to detect prostate cancer and predict the aggressiveness of cancer; however, it is important to consider the bias effect of hemorrhage on the interpretation of MRDW imaging given that hemorrhage affects ADC values.
		                        		
		                        		
		                        		
		                        			Bias (Epidemiology)
		                        			;
		                        		
		                        			Biopsy
		                        			;
		                        		
		                        			Diffusion
		                        			;
		                        		
		                        			Hemorrhage
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Magnetic Resonance Imaging
		                        			;
		                        		
		                        			Magnetic Resonance Spectroscopy
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Neoplasm Grading
		                        			;
		                        		
		                        			Prostate
		                        			;
		                        		
		                        			Prostatic Neoplasms
		                        			;
		                        		
		                        			Retrospective Studies
		                        			
		                        		
		                        	
5.Serial Testing of T-SPOT.TB Assays with Anti-Tuberculosis Therapy in Patients with Extrapulmonay Tuberculosis.
Ki Ho PARK ; Oh Hyun CHO ; Gwang Beum KO ; Yumi LEE ; Hyun Jung PARK ; So Youn PARK ; Song Mi MOON ; Young Pil CHONG ; Sang Oh LEE ; Sang Ho CHOI ; Yang Soo KIM ; Jun Hee WOO ; Sung Han KIM
Infection and Chemotherapy 2011;43(3):245-250
		                        		
		                        			
		                        			BACKGROUND: Limited data are available for the clinical utility of serial interferon-gamma producing T-cell response after initiation of treatment in patients with extrapulmonary tuberculosis (TB). We studied the serial TB-specific antigen T-cell responses measured using the T-SPOT.TB assay during the course of therapy. MATERIALS AND METHODS: We prospectively enrolled adult patients who were newly diagnosed with active extrapulmonary TB over a 24-month period. All patients were given standard anti-TB treatment. Blood samples were obtained for T-SPOT.TB at diagnosis, as well as 1-, 3-, 6-, and 12-months after initiating anti-TB therapy. RESULTS: A total of 52 patients with extrapulmonary TB (38 confirmed and 14 probable TB) were included in the final analysis. All patients had clinical and radiologic improvement after treatment and cured. T-SPOT.TB was positive for 90% at diagnosis, 100% at 1-, 3-, and 6-months, and 93% at 12-months after initiation of anti-TB therapy. There was no significant difference in median T-cell response between early secreting antigenic target-6 (ESAT-6) and culture filtrate protein-10 (CFP-10) at all time points. Median T-cell response steadily increased up to 6 months and then decreased. CONCLUSIONS: T-SPOT.TB assay remained positive after successful anti-TB treatment in most patients with extrapulmonary TB. Our data suggests that serial T-SPOT.TB has limited clinical utility as a surrogate marker of treatment response in patients with extrapulmonary TB.
		                        		
		                        		
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Biomarkers
		                        			;
		                        		
		                        			Enzyme-Linked Immunosorbent Assay
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Interferon-gamma
		                        			;
		                        		
		                        			Prospective Studies
		                        			;
		                        		
		                        			T-Lymphocytes
		                        			;
		                        		
		                        			Tuberculosis
		                        			
		                        		
		                        	
6.Repeatability and Agreement of Macular Thickness Measurement Using Time and Spectral Domain OCT in Diabetic Macular Edema.
Se Beum OH ; Jun Woong MOON ; Hyung Chan KIM
Journal of the Korean Ophthalmological Society 2010;51(3):372-378
		                        		
		                        			
		                        			PURPOSE: To evaluate the repeatability of macular thickness measurements using time domain (TD) OCT and spectral domain (SD) OCT in diabetic macular edema. METHODS: In 42 eyes of 42 patients with diabetic macular edema, three consecutive macular measurements were performed with TD OCT and SD OCT, and measurements for macular thickness and total macular volume obtained by the two OCTs were compared. The within-subject standard deviation (Sw), coefficient of variation (CVw), and intraclass correlation coefficient (ICC) were calculated to assess repeatability, with agreement between measurements assessed with Bland Altman plots. The correlations were also evaluated via the Pearson's correlation coefficient. RESULTS: The Sw of TD OCT and SD OCT for foveal thickness, total macular volume were 29.67 micrometer/16.44 micrometer, 1.26 mm3/0.23 mm3, respectively, and were significantly lower in SD OCT. The ranges of the respective CVw and ICC values were 1.10-2.78%, 0.78~0.96 for TD OCT, and 0.29~0.94%, 0.92~0.99 for SD OCT. The SD OCT showed better repeatability for macular thickness measurements (all p< or =0.001). The 95% limits of agreement for foveal and total macular volume were 88.9 micrometer, 2.4 mm3, respectively. The Pearson's correlation coefficients of macular thickness and total macular volume between the two OCT methods were statistically significant (p=0.88-0.99). CONCLUSIONS: Although both OCTs proved reliable for macular thickness measurements in diabetic macular edema, SD OCT shows better repeatability than TD OCT. Although macular thickness measurements obtained from the two OCTs cannot be used interchangeably, there were statistically significant correlations between measurements obtained using the two OCTs.
		                        		
		                        		
		                        		
		                        			Eye
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Macular Edema
		                        			
		                        		
		                        	
7.Human Umbilical Cord Blood Mononuclear Cell Transplantation in Rats with Intrinsic Sphincter Deficiency.
Joa Jin LIM ; Jin Beum JANG ; Ji Young KIM ; Sung Hwan MOON ; Chung No LEE ; Kyung Jin LEE
Journal of Korean Medical Science 2010;25(5):663-670
		                        		
		                        			
		                        			To evaluate the effectiveness of the human umbilical cord blood (HUCB) transplantation for the treatment of intrinsic sphincter deficiency (ISD), we analyzed the short term effects of HUCB mononuclear cell transplantation in rats with induced-ISD. ISD was induced in rats by electro-cauterization of periurethral soft tissue with HUCB mononuclear cell injection after 1 week. The sphincter function measured by mean leak point pressure was significantly improved in the experimental group compared to the control group at 4 weeks. (91.75+/-18.99 mmHg vs. 65.02+/-22.09 mmHg, P=0.001). Histologically, the sphincter muscle was restored without damage while in the control group it appeared markedly disrupted with atrophic muscle layers and collagen deposit. We identified injected HUCB cells in the tissue sections by Di-I signal and Prussian blue staining. HUCB mononuclear cell injection significantly improved urethral sphincter function, suggesting its potential efficacy in the treatment of ISD.
		                        		
		                        		
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Cells, Cultured
		                        			;
		                        		
		                        			Cord Blood Stem Cell Transplantation/*methods
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Leukocytes, Mononuclear/*transplantation
		                        			;
		                        		
		                        			Rats
		                        			;
		                        		
		                        			Rats, Sprague-Dawley
		                        			;
		                        		
		                        			Treatment Outcome
		                        			;
		                        		
		                        			Urinary Incontinence, Stress/diagnosis/*physiopathology/*surgery
		                        			;
		                        		
		                        			Urologic Surgical Procedures/*methods
		                        			
		                        		
		                        	
8.Comparison of Effects of Intravitreal Triamcinolone and Bevacizumab in the Treatment of Diabetic Macular Edema.
Se Beum OH ; Jun Woong MOON ; Hyung Chan KIM
Journal of the Korean Ophthalmological Society 2009;50(8):1190-1196
		                        		
		                        			
		                        			PURPOSE: To compare the effect of an intravitreal injection of triamcinolone acetonide with bevacizumab in the treatment of diabetic macular edema (DME). METHODS: For this study, the medical records of patients with diabetic macular edema, who received intravitreal triamcinolone injection (IVTA) or intravitreal bevacizumab injection (IVB), were reviewed. Best corrected visual acuity (BCVA), central macular thickness (CMT) and total macular volume (TMV) were evaluated before injection and at 1 week, 1 month, 2 months, 3 months, and 6 months after injection. The adverse events, such as increased intraocular pressure, and progression of cataract, were also reviewed. RESULTS: A total of 72 eyes from 72 patients, (IVTA: 40 eyes, IVB: 32 eyes) were included in this study. In the IVTA group, BCVA improved significantly at 1 week after injection and was maintained until 3 months after injection. In the IVB group, BCVA improved significantly at 1 week after injection and was maintained until 2 months after injection. In the IVTA group, CMT and TMV decreased significantly at 1 week after injection and were maintained until 3 months after injection, while in the IVB group CMT and TMV were maintained until 2 months after injection. The IVTA group showed significantly better results in visual improvement, CMT and TMV reduction compared to the results of the IVB group, from 1 month to 3 months after injection. In the IVTA group, intraocular pressure increased to more than 25 mmHg in 12.5% of patients during the follow-up period. CONCLUSIONS: While the functional and anatomical improvements are achieved by both IVTA and IVB for diabetic macular edema, the effect of IVTA is more prominent with longer duration than IVB.
		                        		
		                        		
		                        		
		                        			Antibodies, Monoclonal, Humanized
		                        			;
		                        		
		                        			Cataract
		                        			;
		                        		
		                        			Eye
		                        			;
		                        		
		                        			Follow-Up Studies
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Intraocular Pressure
		                        			;
		                        		
		                        			Intravitreal Injections
		                        			;
		                        		
		                        			Macular Edema
		                        			;
		                        		
		                        			Medical Records
		                        			;
		                        		
		                        			Triamcinolone
		                        			;
		                        		
		                        			Triamcinolone Acetonide
		                        			;
		                        		
		                        			Visual Acuity
		                        			;
		                        		
		                        			Bevacizumab
		                        			
		                        		
		                        	
9.Comparison of Effects of Intravitreal Triamcinolone and Bevacizumab in the Treatment of Diabetic Macular Edema.
Se Beum OH ; Jun Woong MOON ; Hyung Chan KIM
Journal of the Korean Ophthalmological Society 2009;50(8):1190-1196
		                        		
		                        			
		                        			PURPOSE: To compare the effect of an intravitreal injection of triamcinolone acetonide with bevacizumab in the treatment of diabetic macular edema (DME). METHODS: For this study, the medical records of patients with diabetic macular edema, who received intravitreal triamcinolone injection (IVTA) or intravitreal bevacizumab injection (IVB), were reviewed. Best corrected visual acuity (BCVA), central macular thickness (CMT) and total macular volume (TMV) were evaluated before injection and at 1 week, 1 month, 2 months, 3 months, and 6 months after injection. The adverse events, such as increased intraocular pressure, and progression of cataract, were also reviewed. RESULTS: A total of 72 eyes from 72 patients, (IVTA: 40 eyes, IVB: 32 eyes) were included in this study. In the IVTA group, BCVA improved significantly at 1 week after injection and was maintained until 3 months after injection. In the IVB group, BCVA improved significantly at 1 week after injection and was maintained until 2 months after injection. In the IVTA group, CMT and TMV decreased significantly at 1 week after injection and were maintained until 3 months after injection, while in the IVB group CMT and TMV were maintained until 2 months after injection. The IVTA group showed significantly better results in visual improvement, CMT and TMV reduction compared to the results of the IVB group, from 1 month to 3 months after injection. In the IVTA group, intraocular pressure increased to more than 25 mmHg in 12.5% of patients during the follow-up period. CONCLUSIONS: While the functional and anatomical improvements are achieved by both IVTA and IVB for diabetic macular edema, the effect of IVTA is more prominent with longer duration than IVB.
		                        		
		                        		
		                        		
		                        			Antibodies, Monoclonal, Humanized
		                        			;
		                        		
		                        			Cataract
		                        			;
		                        		
		                        			Eye
		                        			;
		                        		
		                        			Follow-Up Studies
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Intraocular Pressure
		                        			;
		                        		
		                        			Intravitreal Injections
		                        			;
		                        		
		                        			Macular Edema
		                        			;
		                        		
		                        			Medical Records
		                        			;
		                        		
		                        			Triamcinolone
		                        			;
		                        		
		                        			Triamcinolone Acetonide
		                        			;
		                        		
		                        			Visual Acuity
		                        			;
		                        		
		                        			Bevacizumab
		                        			
		                        		
		                        	
10.Effects and Prognostic Factors of Intravitreal Bevacizumab Injection on Choroidal Neovascularization from Age-Related Macular Degeneration.
Se Beum OH ; Won Bin CHO ; Jun Woong MOON ; Hyung Chan KIM
Journal of the Korean Ophthalmological Society 2009;50(2):202-210
		                        		
		                        			
		                        			PURPOSE: To investigate the effects and prognostic factors related to intravitreal injection of bevacizumab on patients with subfoveal choroidal neovascularization secondary to age-related macular degeneration. METHODS: The medical records of patients who received 3 consecutive intravitreal injections of bevacizumab (1.25 mg/0.05 ml, 6 weeks interval) for subfoveal choroidal neovascularization secondary to age-related macular degeneration and followed up for more than 12 months were reviewed (a total of 31 eyes; male, 20; mean age, 72.3+/-7.5 years). Baseline best corrected visual acuity, foveal thickness, and total macular volume were compared with those after 1, 4, and 12 months. The therapeutic effects were investigated with regard to factors such as age, sex, initial visual acuity, lesion size, subtypes of choroidal neovascularization, pigment epithelial detachment, submacular hemorrhage, and previous history of photodynamic therapy. RESULTS: Initial visual acuity (logMAR), foveal thickness, and total macular volume were 0.74+/-0.49, 320+/-88 microm and 9.50+/-2.99 mm3, respectively. Visual acuity improved to 0.68+/-0.61 (p=0.012), and foveal thickness and total macular volume decreased to 218+/-69 microm and 6.32+/-0.71 mm3 (p<0.001), respectively, at 12 months. Visual improvement was achieved less often in patients who were 75 years or older and who had lesions 3 disc areas or greater and relatively good initial vision at 12 months. CONCLUSIONS: Intravitreal bevacizumab injection has beneficial effects for patients with subfoveal choroidal neovascularization secondary to age-related macular degeneration with regard to function and anatomy. However, it should be noted that visual improvement may be limited in older patients with larger lesions and good initial vision.
		                        		
		                        		
		                        		
		                        			Antibodies, Monoclonal, Humanized
		                        			;
		                        		
		                        			Choroid
		                        			;
		                        		
		                        			Choroidal Neovascularization
		                        			;
		                        		
		                        			Hemorrhage
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Intravitreal Injections
		                        			;
		                        		
		                        			Macular Degeneration
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Medical Records
		                        			;
		                        		
		                        			Photochemotherapy
		                        			;
		                        		
		                        			Vision, Ocular
		                        			;
		                        		
		                        			Visual Acuity
		                        			;
		                        		
		                        			Bevacizumab
		                        			
		                        		
		                        	
            
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