1.Ultrastructure and blood-iris barrier in experimental rubeosis iridis in rabbit.
Myung Kyoo KO ; ll Won PARK ; Young Joon KIM ; Joon Kiu CHOE
Korean Journal of Ophthalmology 1990;4(2):66-72
Iris neovascularization was produced in rabbits by hypotony following repeated aspiration of the vitreous. The hypotony was produced after 0.3 ml of vitreous fluid was aspirated using a 25-gauge needle through the pars plana of 10 rabbits. For the histochemical study, horseradish peroxidase(HRP) was injected through the ear lobe vein. After fixation of the iris tissue, the tissue was treated with diaminobenzidine and examined with both light microscopy and transmission electron microscopy. The newly-formed vessel was abundant, particularly on the upper stroma of the iris. The new vessel formation was evident due to the proliferation of endothelial cells, which may have been derived from preexisting iris vessels. The endothelial cells of the newly-formed vessels revealed prominent villous processes into the vascular lumen, formation of the marginal flap, numerous fenestrations in the endothelial junction, and reaction product onto extravascular space by the cytochemical electron microscopy. These results suggest that hypotony in the rabbit produces the disruption of the blood-iris barrier and the balance between angiogenesis-antiangiogenesis modulation.
Animals
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Biological Transport, Active
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Disease Models, Animal
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Horseradish Peroxidase/diagnostic use
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Iris/*blood supply/*ultrastructure
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Iritis/*pathology
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Neovascularization, Pathologic/*pathology
;
Rabbits
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Vitreous Body/surgery
2.Implantation of posterior chamber intraocular lenses by suture fixation without capsular and zonular support.
Korean Journal of Ophthalmology 1989;3(2):90-93
We implanted sulcus-fixated posterior chamber intraocular lenses (PCL) in three cataractous, six aphakic, and four eyes during penetrating keratoplasty due to corneal opacity in the absence of capsular and zonular support. This technique has been successfully performed in all cases and produced good visual outcome in 12 eyes (93%). In four eyes which had penetrating keratoplasty and the fixation of PCL, one developed vitreous hemorrhage and one developed corneal graft rejection.
Adult
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Aged
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Aphakia/complications/surgery
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Cataract Extraction
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Corneal Opacity/complications/surgery
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Eye Hemorrhage/etiology
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Female
;
Follow-Up Studies
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Graft Rejection
;
Humans
;
Keratoplasty, Penetrating
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Lens Capsule, Crystalline/surgery
;
*Lenses, Intraocular/adverse effects
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Male
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Methods
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Middle Aged
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Refraction, Ocular
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*Suture Techniques
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Visual Acuity
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Vitreous Body/blood supply
3.Intravitreal Bevacizumab (Avastin) Treatment of Neovascular Glaucoma in Ocular Ischemic Syndrome.
Sang Joon LEE ; Jung Joo LEE ; Soo Young KIM ; Shin Dong KIM
Korean Journal of Ophthalmology 2009;23(2):132-134
We report a case of ocular ischemic syndrome accompanied by neovascular glaucoma that was successfully treated with Bevacizumab. A 70-year-old male patient diagnosed with neovascular glaucoma of the left eye 3-4 years prior complained of continuous left eye pain and declining visual acuity despite receiving the latest treatment methods. At the time of admission the patient had no light perception in the left eye and his intraocular pressure was 30 mmHg. Anterior segment and fundus examinations revealed neovascularization of the iris and stenosis of the retinal vessel. Hypofluorescence of the choroid and retinal vessels was observed on fluorescence fundus angiography. Left internal carotid artery stenosis was observed on a brain MRI. Despite being treated with eye solution and oral medication, intraocular pressure was not controlled. After 7 days, we performed an intravitreal Bevacizumab 1.25 mg/0.05mL injection. One day after the intravitreal Bevacizumab injection, the neovascularization had nearly regressed and intraocular pressure was 30 mmHg. Intravitreal Bevacizumab injection produced regression of neovascularization and proved effective for treatment of neovascular glaucoma in this case of ocular ischemic syndrome.
Aged
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Angiogenesis Inhibitors/*administration & dosage
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Antibodies, Monoclonal/*administration & dosage
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Carotid Stenosis/*complications/diagnosis
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Diagnosis, Differential
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Eye/*blood supply
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Fluorescein Angiography
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Fundus Oculi
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Glaucoma, Neovascular/diagnosis/*drug therapy/etiology
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Humans
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Injections
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Ischemia/*complications/diagnosis
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Magnetic Resonance Angiography
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Male
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Vascular Endothelial Growth Factor A
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Vitreous Body
4.Intravitreal Bevacizumab (Avastin) Treatment of Neovascular Glaucoma in Ocular Ischemic Syndrome.
Sang Joon LEE ; Jung Joo LEE ; Soo Young KIM ; Shin Dong KIM
Korean Journal of Ophthalmology 2009;23(2):132-134
We report a case of ocular ischemic syndrome accompanied by neovascular glaucoma that was successfully treated with Bevacizumab. A 70-year-old male patient diagnosed with neovascular glaucoma of the left eye 3-4 years prior complained of continuous left eye pain and declining visual acuity despite receiving the latest treatment methods. At the time of admission the patient had no light perception in the left eye and his intraocular pressure was 30 mmHg. Anterior segment and fundus examinations revealed neovascularization of the iris and stenosis of the retinal vessel. Hypofluorescence of the choroid and retinal vessels was observed on fluorescence fundus angiography. Left internal carotid artery stenosis was observed on a brain MRI. Despite being treated with eye solution and oral medication, intraocular pressure was not controlled. After 7 days, we performed an intravitreal Bevacizumab 1.25 mg/0.05mL injection. One day after the intravitreal Bevacizumab injection, the neovascularization had nearly regressed and intraocular pressure was 30 mmHg. Intravitreal Bevacizumab injection produced regression of neovascularization and proved effective for treatment of neovascular glaucoma in this case of ocular ischemic syndrome.
Aged
;
Angiogenesis Inhibitors/*administration & dosage
;
Antibodies, Monoclonal/*administration & dosage
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Carotid Stenosis/*complications/diagnosis
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Diagnosis, Differential
;
Eye/*blood supply
;
Fluorescein Angiography
;
Fundus Oculi
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Glaucoma, Neovascular/diagnosis/*drug therapy/etiology
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Humans
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Injections
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Ischemia/*complications/diagnosis
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Magnetic Resonance Angiography
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Male
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Vascular Endothelial Growth Factor A
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Vitreous Body
5.Intravitreal bevacizumab for the treatment of myopic choroidal neovascularisation in an Asian population.
Boon Kwang LOH ; Shu Yen LEE ; Jacob CHENG ; Ian YEO ; Doric WONG ; Chong Lye ANG
Annals of the Academy of Medicine, Singapore 2010;39(6):493-494
Aged
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Angiogenesis Inhibitors
;
administration & dosage
;
pharmacology
;
therapeutic use
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Antibodies, Monoclonal
;
administration & dosage
;
pharmacology
;
therapeutic use
;
Antibodies, Monoclonal, Humanized
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Asia
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ethnology
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Bevacizumab
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Choroidal Neovascularization
;
drug therapy
;
ethnology
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Female
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Humans
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Male
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Middle Aged
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Myopia
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physiopathology
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Prospective Studies
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Treatment Outcome
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Vitreous Body
;
blood supply
6.The Therapeutic Effects of Bevacizumab in Patients with Polypoidal Choroidal Vasculopathy.
Sun Young LEE ; June Gone KIM ; Soo Geun JOE ; Hyewon CHUNG ; Young Hee YOON
Korean Journal of Ophthalmology 2008;22(2):92-99
PURPOSE: To evaluate the efficacy and safety of intravitreal bevacizumab for polypoidal choroidal vasculopathy (PCV). METHODS: In this retrospective interventional pilot study, 12 eyes of 11 patients with active PCV were treated with intravitreal bevacizumab (1.25 mg) alone or in combination with photodynamic therapy (PDT) depending on the informed patient's choice. Intravitreal bevacizumab was repeated at 6-week intervals until the regression of active lesion was detected on fluorescein angiography (FA) which was done on a regular basis, Indocyanine green angiography (ICGA) and optical coherence tomography (OCT) analyses. RESULTS: Intravitreal bevacizumab was given alone in 8 eyes (Group 1) and in combination with PDT in 4 eyes (Group 2). Mean follow-up duration was 17 weeks in group 1 and 15 weeks in group 2 after bevacizumab treatment. The mean number of bevacizumab injections was 2.2 in group 1 and 2.5 in group 2. Mean BCVA improved from 20/63 to 20/40 in group 1 and 20/63 to 20/32 in group 2. Of all eyes, the BCVA improved by > or =2 lines in seven (58%) eyes and resolution of fluid and hemorrhages in clinical examination, an absence of leakage on repeat FAs, or resolved pigment epithelial detachment (PED) and/or subretinal fluid (SRF) on OCT exam was confirmed in 10 (83%) eyes. Partial or complete regression of the polypoidal vessels and interconnecting vessels was reported for most cases at the last follow-up. No significant ocular or systemic side effects were observed in both groups. CONCLUSIONS: Short-term results indicate that intravitreal bevacizumab (1.25 mg) alone or in combination with PDT is well tolerated and associated with improvement in BCVA and reduced angiographic leakage in most patients. Further evaluation of intravitreal bevacizumab therapy for the treatment of PCV is warranted.
Aged
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Aged, 80 and over
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Angiogenesis Inhibitors/adverse effects/*therapeutic use
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Antibodies, Monoclonal/adverse effects/*therapeutic use
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Choroid/*blood supply/pathology
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Coloring Agents/diagnostic use
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Combined Modality Therapy
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Female
;
Fluorescein Angiography
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Humans
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Indocyanine Green/diagnostic use
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Injections
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Male
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Middle Aged
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Peripheral Vascular Diseases/diagnosis/*drug therapy/physiopathology
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*Photochemotherapy
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Pilot Projects
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Retrospective Studies
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Tomography, Optical Coherence
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Treatment Outcome
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Vascular Endothelial Growth Factor A/antagonists & inhibitors
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Visual Acuity/physiology
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Vitreous Body