1.Transscleral Diode Laser Photocoagulation for Retinopathy of Prematurity: Short-term Structural Outcome.
Hee Joon CHO ; Jae Hak BAE ; Young Wook CHO
Journal of the Korean Ophthalmological Society 2001;42(12):1697-1704
PURPOSE: We observed the short-term outcome and associated complications of transscleral diode laser photocoagulation (TSDL) for acute proliferative retinopathy of prematurity (ROP) to evaluate the efficacy and safety. METHODS: 20 eyes of 10 infants with acute ROP were treated with transscleral diode laser photo-coagulation through conjunctiva by a single surgeon. Anatomical results and postoperative complications were main outcomes. Follow-up ranged from 11 to 40 weeks. RESULTS: In 1 eye (5%), there was a macular temporal dragging. In 19 eyes (95%), regression occurred after a single laser treatment with a flat retina. No significant anterior or posterior segment complications were occurred, even though there was a small amount of preretinal hemorrhage in 1 eye after laser photocoagulation. CONCLUSIONS: The results suggest that transscleral diode laser photocoagulation is a safe and effective alternative to cryotherapy or transpupillary diode laser photocoagulation in the treatment of ROP.
Conjunctiva
;
Cryotherapy
;
Follow-Up Studies
;
Hemorrhage
;
Humans
;
Infant
;
Lasers, Semiconductor*
;
Light Coagulation*
;
Postoperative Complications
;
Retina
;
Retinopathy of Prematurity*
2.A study of behavioral aspect for the health promotion among physician and general population.
Jeong Yeol OH ; Young Mee LEE ; Hak Eun SUH ; Kyung Hwan CHO ; Myung Ho HONG
Journal of the Korean Academy of Family Medicine 1992;13(11):879-890
No abstract available.
Health Promotion*
3.Three Cases of Congenital Aniridia in One Family.
Jae Hak BAE ; Young Wook CHO ; Mi Sun KWAK
Journal of the Korean Ophthalmological Society 2000;41(1):282-287
Aniridia is a relatively rare congenital anomaly and its incidence is about 1:100, 000.Main features of aniridia include congenitally partial or nearly complete absence of the iris and hypoplasia of optic disc and fovea. It is almost bilateral and occurred as an autosomal dominant trait.However, some patients develop both sporadic nonfamilial aniridia and Wilms 'tumor, and another group of patients is transmitted as an autosomal recessive trait. We observed aniridia in two generations, as mother and two daughters. They had cataract, nystagmus, neovascularization of corneal margin and pannus formation, as well as aniridia.We also found hypoplasia of optic disc and fovea in mother. We have operated on mother with phacoemulsified lens aspiration and posterior chamber IOL implantation in both eyes consecutively.The postoperative visual acuity following lens extraction improved, but was not corrected. In addition, intraocular pressure decreased.
Aniridia*
;
Cataract
;
Family Characteristics
;
Humans
;
Incidence
;
Intraocular Pressure
;
Iris
;
Mothers
;
Nuclear Family
;
Visual Acuity
4.IgG4-Related Sclerosing Sialadenitis: Report of Three Cases.
Ji Seon BAE ; Joo Young KIM ; Sang Hak HAN ; Seung Ho CHOI ; Kyung Ja CHO
Korean Journal of Pathology 2011;45(Suppl 1):S36-S40
Chronic sclerosing sialadenitis, Mikulicz disease or Kuttner tumor has been recently recognized as a spectrum of IgG4-related sclerosing disease. IgG4-related disease is characterized by a high serum IgG4 level and tissue infiltration of IgG4-positive plasmacytes. We report three cases of chronic sclerosing sialadenitis with variably associated systemic involvement. All patients presented with a submandibular mass or swelling, and all the resected submandibular glands showed diffuse lymphocytic infiltration, lymphoid follicles, and septal fibrosis. Two of the specimens revealed numerous IgG-positive plasma cells, most of which were IgG4-positive on immunohistochemical staining. One of them was associated with dacryoadenitis and hypophysitis. The other patient had ureterorenal lesions. Immunohistochemical study was unavailable in remaining one case, but the histologic features along with elevated IgG level and associated pancreatitis supported the diagnosis. All patients received steroid therapy postoperatively and are doing well. Salivary gland involvement in IgG4-related fibrosclerosis should be recognized in systemic medical pathology.
Dacryocystitis
;
Fibrosis
;
Humans
;
Immunoglobulin G
;
Mikulicz' Disease
;
Pancreatitis
;
Plasma Cells
;
Salivary Glands
;
Sialadenitis
;
Submandibular Gland
5.A case of paraquat poisoning in child.
Min Yong OUM ; Sung Ik CHO ; Young Chang KIM ; Hak Ju CHA ; Sang Jhoo LEE
Journal of the Korean Pediatric Society 1989;32(11):1540-1545
No abstract available.
Child*
;
Humans
;
Paraquat*
;
Poisoning*
6.Clinical significance of uric acid during pregnancy inducedhypertension.
Young Woo JUNG ; Eun Bea RHO ; Hak Hee LEE ; Young Chul KIM ; Sung Jin CHO ; Chan Young PARK
Korean Journal of Obstetrics and Gynecology 1991;34(11):1529-1534
No abstract available.
Pregnancy*
;
Uric Acid*
7.Relation between Coronary Artery Cross Sectional Area and Left Ventricular Wall Mass.
Doo Hong CHOI ; Hak Sun KIM ; Sun Ho CHANG ; Joo Young CHO ; Sung Gu KIM ; Young Joo KWON
Korean Circulation Journal 1990;20(4):748-752
The coronary artery cross sectional area (CSA) is proportional to LV mass. We have measured the cross sectional area of the left and right coronary arteries in patients with ischemic heart disease to see whether it is related to the change in the LV mass. The following results were obtained ; 1) There were no significant difference in mean CSA of coronary arteries and LV mass determined by echocardiography and cineangiography between control and ischemic heart disease. 2) There were significantly increased ratio of left ventricular mass by cineangiogram to CSA of left anterior descending coronary artery in patients with myocardial infarction as compared with control group. 3) A linear relation between LV mass by cineangiogram and CSA of left coronary artery was noted in control group (r=0.53, P<0.05) and ischemic heart disease group (r=0.51, P<0.05). 4) A linear relation between LV mass determined by echocardiography and CSA of left coronary artery was noted in control group (r=0.55, P<0.05).
Cineangiography
;
Coronary Vessels*
;
Echocardiography
;
Humans
;
Myocardial Infarction
;
Myocardial Ischemia
8.Local Production of IgE in Nasal Polyp.
Chung Hyun CHO ; Tae Young JANG ; Young Seok YUN ; Dong Hak JUNG
Journal of Rhinology 1997;4(2):126-128
Among the several possible etiologic factors for the development of nasal polyp, localized nasal allergy had been insisted to be one of the major factors. This study aims to explore the existence of local production of IgE within nasal polyp, which can be the indirect evidence of localized nasal allergy. Fifty-two patients, who underwent nasal polypectomies between April 1993 and December 1995, were selected. The levels of total IgE and specific IgE of serum and polyp fluids were assessed. By using Donovan's equation, the percentage of local production of IgE in nasal polyp were calculated. Local production of total IgE was demonstrated in 18 cases of 28 polyp patient group (64.3%). Local production of specific IgE for Dermatophagoides pteronyssinus and Dermatophagoides farinae were demonstrated in 6 cases of 24 polyp patient group (25%). These results suggest the existence of local production of IgE in nasal polyp.
Dermatophagoides farinae
;
Dermatophagoides pteronyssinus
;
Humans
;
Hypersensitivity
;
Immunoglobulin E*
;
Nasal Polyps*
;
Polyps
9.Bilateral Second Branchial Cleft Fistulas: A Case Report.
Young Hak PARK ; Jeong Hak LEE ; Jong Hyung KIM ; Seung Ho CHO
Korean Journal of Otolaryngology - Head and Neck Surgery 2005;48(5):676-679
The branchiogenic anomalies are common congenital cervical anomalies. They usually arise from an incomplete obliteration of the branchial apparatus during fetal development. These anomalies may be confused with and mistaken for other potentially more serious lesions, such as cystic hygromas, teratomas, and lymphomas. The anomalies are typically discovered in the pediatric and adolescent population and develop unilaterally. Bilateral manifestations are very rare and have a familial tendency. In addition, anomalies such as intrauterine and postnasal growth retardation, premature aging and unusual faces may be related with bilateral occurrence. This is the first report in the Korean language literature of bilateral branchial fistulas.
Adolescent
;
Aging, Premature
;
Branchial Region*
;
Fetal Development
;
Fistula*
;
Humans
;
Lymphangioma, Cystic
;
Lymphoma
;
Teratoma
10.Cosmetic Repair of Nevus of Ota.
Bum Joo CHO ; Young Keun HAN ; Joo Hak KIM ; Won Ryang WEE ; Jin Hak LEE ; Ji Won KWON
Journal of the Korean Ophthalmological Society 2006;47(6):996-999
PURPOSE: To report a case of cosmetically successful treatment of nevus of Ota performed by scleral painting and scleral allograft transplantation. METHODS: Scleral painting and allograft transplantation were done in a 28-year-old woman who had cosmetic problem due to nevus of Ota, and she was followed up for 5 months postoperatively. RESULTS: The patient had no specific postoperative complication and was satisfied with the surgical results. CONCLUSIONS: For patients of nevus of Ota who have not been treated successfully, scleral painting and allograft transplation can be an effective cosmetic treatment.
Adult
;
Allografts
;
Female
;
Humans
;
Nevus of Ota*
;
Nevus*
;
Paint
;
Paintings
;
Postoperative Complications