1.A Case of Congenital Simple Hamartoma of the Retinal Pigment Epithelium and Coats' Disease in the Same Eye.
Won Jae HEO ; Dong Ho PARK ; Jae Pil SHIN
Korean Journal of Ophthalmology 2015;29(4):282-283
No abstract available.
Diagnosis, Differential
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Fluorescein Angiography
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Fundus Oculi
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Hamartoma/*congenital/diagnosis
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Humans
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Male
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Retinal Diseases/*congenital/diagnosis
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Retinal Pigment Epithelium/*pathology
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Retinal Telangiectasis/*diagnosis
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Tomography, Optical Coherence
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Young Adult
2.Stage 3B Coats disease in a premature and low-birth-weight infant.
Hu-Ping SONG ; Hua AI ; Qi ZHU ; Chun-Ling LEI ; Jian-Zhou WANG ; Xiao-Qin LEI
Chinese Medical Journal 2012;125(20):3759-3760
3.The Clinical Analysis and Treatment Results of Coats' Disease in Children.
Eui Seok HAN ; Ho Kyung CHOUNG ; Jang Won HEO ; Seong Joon KIM ; Young Suk YU
Journal of the Korean Ophthalmological Society 2006;47(3):423-430
PURPOSE: To evaluate the clinical characteristics and treatment result of Coats' disease in children. METHODS: Data on demographics, clinical presentation, and ocular findings were analyzed for 67 eyes of 67 patients with Coats' disease by retrospective chart review. Among these, treatment results were analyzed from 56 eyes which had received local treatment or subretinal fluid drainage (SRFD). Treatment was considered successful when telangiectatic vessels or exudates had regressed after local treatment or when pupillary block glaucoma was treated or prevented after SRFD. RESULTS: Mean age at diagnosis was 5.0 years (5 months-15 years) and 90% were males. 67% of retinal telangiectasias were located in the temporal. There were exudative retinal detachments in 46 (69%) eyes. Among them, SRFD was performed in 19 (28%) to treat or prevent pupillary block glaucoma. The mean age at diagnosis of patients that underwent treatment was 5.1 years. In 37 of 56 patients, 95% of retinal telangiectasias were regressed after primary local treatment, and 21 eyes (31%) underwent SRFD. Management of glaucoma was achieved after SRFD in 16 patients, and one more SRFD was needed after primary SRFD in 5 patients. CONCLUSIONS: In Coats' disease, it is necessary to eradicate retinal telangiectasia with local treatment and to follow up carefully for secondary glaucoma, which can be treated with SRFD in cases of severe exudative retinal detachment.
Child*
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Cryotherapy
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Demography
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Diagnosis
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Drainage
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Exudates and Transudates
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Follow-Up Studies
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Glaucoma
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Humans
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Male
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Retinal Detachment
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Retinaldehyde
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Retrospective Studies
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Subretinal Fluid
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Telangiectasis
4.Demographic Features of Idiopathic Macular Telangiectasia in Korean Patients.
Sung Hyun KIM ; Jaeryung OH ; Soh Eun AHN ; Choul Yong PARK ; Jong Hyun OH
Korean Journal of Ophthalmology 2015;29(3):155-159
PURPOSE: To investigate the clinical and demographic features of idiopathic macular telangiectasia (MacTel) in Korean patients since the introduction of spectral domain optical coherence tomography (SD-OCT). METHODS: We reviewed medical records of patients who were diagnosed with MacTel from 2009 to 2013. All patients underwent fluorescein angiography and SD-OCT and were classified as type 1 or type 2 according to the classification system proposed by Yannuzzi. RESULTS: Over a period of 5 years, 4 (18.2%) patients were diagnosed with type 1 MacTel and 18 (81.8%) patients were diagnosed with type 2 MacTel. All patients with type1 MacTel were male, and their mean age was 51 +/- 8.6 years. Among patients with type 2 MacTel, 3 (16.7%) were male, 15 (83.3%) were female, and the mean age was 60 +/- 13.6 years. Whereas all type 1 MacTel patients had either metamorphopsia or mild scotoma, of the 18 patients with type 2 MacTel, only 4 (22.2%) had those symptoms, 10 (55.6%) complained of only mild visual impairment, and the other 4 (22.2%) had no symptoms. Intraretinal cystoid spaces were observed in 26 (72.2%) of 36 eyes with type 2 MacTel by SD-OCT. These cystoid spaces had irregular boundaries and did not correspond to angiographic leakages. CONCLUSIONS: Type 2 MacTel was most common in the present study. The wider availability of SD-OCT may have contributed to the diagnosis of type 2 MacTel. Type 2 MacTel may be more prevalent than type 1 in Koreans, which corresponds to the results of Western countries.
Adult
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Aged
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Aged, 80 and over
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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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Republic of Korea/epidemiology
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Retina/pathology
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*Retinal Telangiectasis/diagnosis/epidemiology/pathology/physiopathology
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Retrospective Studies
5.Demographic Features of Idiopathic Macular Telangiectasia in Korean Patients.
Sung Hyun KIM ; Jaeryung OH ; Soh Eun AHN ; Choul Yong PARK ; Jong Hyun OH
Korean Journal of Ophthalmology 2015;29(3):155-159
PURPOSE: To investigate the clinical and demographic features of idiopathic macular telangiectasia (MacTel) in Korean patients since the introduction of spectral domain optical coherence tomography (SD-OCT). METHODS: We reviewed medical records of patients who were diagnosed with MacTel from 2009 to 2013. All patients underwent fluorescein angiography and SD-OCT and were classified as type 1 or type 2 according to the classification system proposed by Yannuzzi. RESULTS: Over a period of 5 years, 4 (18.2%) patients were diagnosed with type 1 MacTel and 18 (81.8%) patients were diagnosed with type 2 MacTel. All patients with type1 MacTel were male, and their mean age was 51 +/- 8.6 years. Among patients with type 2 MacTel, 3 (16.7%) were male, 15 (83.3%) were female, and the mean age was 60 +/- 13.6 years. Whereas all type 1 MacTel patients had either metamorphopsia or mild scotoma, of the 18 patients with type 2 MacTel, only 4 (22.2%) had those symptoms, 10 (55.6%) complained of only mild visual impairment, and the other 4 (22.2%) had no symptoms. Intraretinal cystoid spaces were observed in 26 (72.2%) of 36 eyes with type 2 MacTel by SD-OCT. These cystoid spaces had irregular boundaries and did not correspond to angiographic leakages. CONCLUSIONS: Type 2 MacTel was most common in the present study. The wider availability of SD-OCT may have contributed to the diagnosis of type 2 MacTel. Type 2 MacTel may be more prevalent than type 1 in Koreans, which corresponds to the results of Western countries.
Adult
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Aged
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Aged, 80 and over
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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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Republic of Korea/epidemiology
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Retina/pathology
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*Retinal Telangiectasis/diagnosis/epidemiology/pathology/physiopathology
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Retrospective Studies
6.Combined Photodynamic Therapy and Intravitreal Bevacizumab Injection for the Treatment of Adult Coats' Disease: A Case Report.
Jongshin KIM ; Kyu Hyung PARK ; Se Joon WOO
Korean Journal of Ophthalmology 2010;24(6):374-376
A 68-year-old woman presented with a visual field defect in her right eye. The fundus of her right eye showed multiple telangiectatic vessels, retinal hemorrhages, and subretinal exudates in the inferior peripheral retina. Nine months later, the subretinal exudates extended to the fovea despite treatment with laser photocoagulation. Cryotherapy was not possible at the time because of the posterior location of the retinal telangiectatic vessels. She was treated with a combination of photodynamic therapy (PDT) and intravitreal bevacizumab injection: three injections were given at 2-month intervals. After this combined therapy, her right fundus revealed a significant regression of abnormal retinal vessels and subretinal exudates. A fluorescein angiography showed no leakage from the abnormal retinal vessels. At 9 months after the combined therapy, she was able to maintain a stable visual acuity and visual field. This is the first case report that demonstrates the efficacy of the combined treatment of PDT and intravitreal bevacizumab injection in Coats's disease. This combined therapy is a kind of treatment modality for adult Coats' disease in cases which cryotherapy cannot be employed and are refractory to laser photocoagulation.
Aged
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Angiogenesis Inhibitors/*administration & dosage
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Antibodies, Monoclonal/*administration & dosage
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Drug Therapy, Combination
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Female
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Fluorescein Angiography
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Fundus Oculi
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Humans
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Intravitreal Injections
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*Photochemotherapy
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Retinal Telangiectasis/diagnosis/*drug therapy/physiopathology
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Treatment Outcome
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Visual Fields
7.Clinical Features of Idiopathic Juxtafoveal Telangiectasis in Koreans.
Seung Woo LEE ; Sung Min KIM ; Yun Taek KIM ; Se Woong KANG
Korean Journal of Ophthalmology 2011;25(4):225-230
PURPOSE: To describe the clinical characteristics of idiopathic juxtafoveal telangiectasis (IJT) in Koreans. METHODS: Medical records of 16 patients with IJT were analyzed during the period from 1997 to 2009. Diagnosis was based on biomicrosopic and fluorescein angiographic findings and the group was determined according to the Gass and Blodi classification. RESULTS: We analyzed eight patients in group 1A (50%), two in group 1B (12.5%), and six in group 2A (37.5%). Diverse treatment modalities, such as macular laser photocoagulation, photodynamic therapy, intravitreal antiangiogenic agent, and steroid injection, were applied for macular edema in nine eyes; however, only two eyes showed visual improvement. CONCLUSIONS: In this case series, group 1A was the most common. For macular edema related to IJT, current treatment strategies had no consistent effect.
Adolescent
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Adult
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Aged
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Angiogenesis Inhibitors/administration & dosage
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Child
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Female
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Fluorescein Angiography
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Follow-Up Studies
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Fovea Centralis/*blood supply
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Fundus Oculi
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Glucocorticoids/administration & dosage
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Humans
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Incidence
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Intravitreal Injections
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Male
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Microscopy, Acoustic
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Middle Aged
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Photochemotherapy/methods
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Prognosis
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Republic of Korea/epidemiology
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Retinal Diseases/*diagnosis/drug therapy/epidemiology
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Retinal Vessels/*pathology/ultrasonography
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Retrospective Studies
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Risk Factors
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Telangiectasis/*diagnosis/drug therapy/epidemiology
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Visual Acuity
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Young Adult