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1.
J AAPOS ; 17(5): 521-3, 2013 Oct.
Article in English | MEDLINE | ID: mdl-24054036

ABSTRACT

Children treated for toxoplasma retinochoroiditis may experience a range of severe adverse drug responses. Drug reaction with eosinophilia and systemic symptoms syndrome is a life-threatening idiosyncratic drug reaction with a 10% mortality. We present a case of drug reaction with eosinophilia and systemic symptoms syndrome in a child on standard combination treatment with oral sulfadiazine, pyrimethamine, folinic acid, and steroids for toxoplasma retinochoroiditis. Early clinical recognition and appropriate treatment led to a complete recovery and no longterm sequelae. The parents of children during sulfadiazine treatment should be counseled on the potential significance of nonspecific illness.


Subject(s)
Antiprotozoal Agents/adverse effects , Chorioretinitis/drug therapy , Drug Hypersensitivity/etiology , Eosinophilia/chemically induced , Toxoplasmosis, Ocular/drug therapy , Adolescent , Drug Eruptions/etiology , Drug Therapy, Combination , Female , Humans , Leucovorin/adverse effects , Pyrimethamine/adverse effects , Steroids/adverse effects , Sulfadiazine/adverse effects
2.
J AAPOS ; 7(1): 23-7, 2003 Feb.
Article in English | MEDLINE | ID: mdl-12690365

ABSTRACT

BACKGROUND: Acquired Brown syndrome is known to occur after trauma, iatrogenic events, cysts of superior oblique muscle tendon, and inflammation. The purpose of this study is to report a large series of patients with acquired Brown syndrome secondary to superior oblique muscle cysticercosis and to discuss its management. METHODS: Retrospective analysis was performed of clinical and imaging features, management, and outcome in seven patients with cysticercosis of the superior oblique muscle presenting clinically as Brown syndrome. RESULTS: Seven patients were identified (five male and two female) ranging in age from 6 to 45 years. All patients had the ocular motility limitation, ie, limitation of elevation in adduction., characteristic of Brown syndrome. This was associated with pain and swelling in the superior nasal orbit. Diagnosis was established by observing the cysticercus cyst with scolex on imaging (ultrasound B scan, magnetic resonance imaging, and/or computed tomography). Oral albendazole (15 mg/kg) and oral prednisolone (1mg/kg) were given for 4 weeks, and the patients were followed up for 1 year. Clinical recovery with improvement of ocular motility and regression of imaging features was noted in all patients. CONCLUSIONS: Acquired Brown syndrome secondary to superior oblique muscle cysticercosis is a rare entity. Awareness of this condition, which leads to early diagnosis and institution of prompt medical treatment, results in a successful clinical outcome.


Subject(s)
Cysticercosis/complications , Ocular Motility Disorders/parasitology , Oculomotor Muscles/parasitology , Adolescent , Adult , Anthelmintics/therapeutic use , Child , Cysticercosis/drug therapy , Female , Fixation, Ocular , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Ocular Motility Disorders/diagnosis , Ocular Motility Disorders/physiopathology , Retrospective Studies , Tomography, X-Ray Computed , Treatment Outcome , Ultrasonography
3.
J AAPOS ; 7(6): 389-95, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14730290

ABSTRACT

BACKGROUND: Duane syndrome is characterized by abduction deficiency, narrowing of the palpebral fissure with retraction of globe on attempted adduction, and upshoot or downshoot, which can be the most prominent feature of the motility disorder. The upshoot and downshoot is believed to be caused by a tautness or leash effect from the lateral rectus muscle. The purpose of this study was to present the results of recession of the lateral rectus muscle with Y-splitting in the treatment of upshoot and downshoot in Duane syndrome. METHODS: Ten patients with Duane syndrome underwent surgery for severe upshoot or downshoot. Lateral rectus muscles recession from 5.0 to 9.0 mm and Y-splitting was accomplished in all patients. In 6 patients, the medial rectus muscles were recessed simultaneously from 5.0 to 6.0 mm to correct the associated marked globe retraction and ocular deviation. RESULTS: Mean age at the time of surgery was 9.9 +/- 6.9 years (range, 3 to 20). Median follow up was 6 months (range, 3 weeks to 3 years). After surgery, all patients showed a marked decrease in upshoot or downshoot as well as improvement in globe retraction and face turn, where present. CONCLUSIONS: Recession of lateral rectus muscle with Y-splitting is an extremely effective procedure in the treatment of significant upshoot and downshoot associated with globe retraction in Duane syndrome. When combined with simultaneous recession of the medial rectus muscle, it improves globe retraction and corrects ocular deviation.


Subject(s)
Duane Retraction Syndrome/surgery , Oculomotor Muscles/surgery , Ophthalmologic Surgical Procedures/methods , Adolescent , Adult , Child , Child, Preschool , Duane Retraction Syndrome/physiopathology , Eye Movements/physiology , Female , Humans , Male , Oculomotor Muscles/physiopathology , Treatment Outcome , Vision, Binocular
4.
Invest Ophthalmol Vis Sci ; 43(3): 615-22, 2002 Mar.
Article in English | MEDLINE | ID: mdl-11867575

ABSTRACT

PURPOSE: To assess the prevalence of refractive error and related visual impairment in school-aged children in the rural population of the Mahabubnagar district in the southern Indian state of Andhra Pradesh. METHODS: Random selection of village-based clusters was used to identify a sample of children 7 to 15 years of age. From April 2000 through February 2001, children in the 25 selected clusters were enumerated in a door-to-door survey and examined at a rural eye center in the district. The examination included visual acuity measurements, ocular motility evaluation, retinoscopy and autorefraction under cycloplegia, and examination of the anterior segment, media, and fundus. Myopia was defined as spherical equivalent refractive error of at least -0.50 D and hyperopia as +2.00 D or more. Children with reduced vision and a sample of those with normal vision underwent independent replicate examinations for quality assurance in seven clusters. RESULTS: A total of 4414 children from 4876 households was enumerated, and 4074 (92.3%) were examined. The prevalence of uncorrected, baseline (presenting), and best corrected visual acuity of 20/40 or worse in the better eye was 2.7%, 2.6%, and 0.78%, respectively. Refractive error was the cause in 61% of eyes with vision impairment, amblyopia in 12%, other causes in 15%, and unexplained causes in the remaining 13%. A gradual shift toward less-positive values of refractive error occurred with increasing age in both boys and girls. Myopia in one or both eyes was present in 4.1% of the children. Myopia risk was associated with female gender and having a father with a higher level of schooling. Higher risk of myopia in children of older age was of borderline statistical significance (P = 0.069). Hyperopia in at least one eye was present in 0.8% of children, with no significant predictors. CONCLUSIONS: Refractive error was the main cause of visual impairment in children aged between 7 and 15 years in rural India. There was a benefit of spectacles in 70% of those who had visual acuity of 20/40 or worse in the better eye at baseline examination. Because visual impairment can have a significant impact on a child's life in terms of education and development, it is important that effective strategies be developed to eliminate this easily treated cause of visual impairment.


Subject(s)
Refractive Errors/epidemiology , Rural Population/statistics & numerical data , Adolescent , Age Distribution , Child , Eyeglasses , Female , Humans , India/epidemiology , Male , Prevalence , Random Allocation , Refractive Errors/therapy , Risk Factors , Sex Distribution , Vision Disorders/epidemiology , Visual Acuity
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