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2.
Trans Am Ophthalmol Soc ; 103: 116-23; discussuin 123-5, 2005.
Article in English | MEDLINE | ID: mdl-17057795

ABSTRACT

PURPOSE: Macular schisis or detachment is frequently observed in eyes with optic pits or colobomas. Although spontaneous resolution of the maculopathy has been reported, concurrent changes in the optic nerve coloboma have not. We report three cases of atypical optic nerve colobomas in which dynamic optic nerve changes coincide with the development and subsequent resolution of the associated maculopathy. METHODS: We reviewed the records of three patients with dynamic optic nerve changes associated with maculopathy. All patients were observed for at least 6 months. Fundus photography and fluorescein angiography were used to document the optic nerve and macular changes. RESULTS: Three patients were noted to have macular detachments without apparent optic nerve excavation. With observation, the maculopathy spontaneously resolved in each case. We documented concurrent optic nerve changes whereby atypical optic nerve colobomas became apparent over several months in all cases. In one case, we noted the simultaneous development of maculopathy in association with obscuration of a prior disc anomaly. None of the eyes had a posterior vitreous detachment. We could not identify any associated systemic conditions or reproduce the findings with external stimulation. Initial Snellen acuity ranged from 20/60 to 20/200. Final Snellen acuity ranged from 20/20 to 20/40. CONCLUSIONS: Fluctuating optic nerve changes may occur in the setting of atypical optic nerve coloboma and associated maculopathy. In cases of macular schisis or detachment where an optic nerve coloboma is not readily apparent, and no other causes are identified, consideration of a period of observation prior to therapeutic intervention seems appropriate.


Subject(s)
Coloboma/complications , Macula Lutea , Optic Nerve Diseases/complications , Retinal Detachment/complications , Adult , Coloboma/pathology , Coloboma/physiopathology , Female , Fundus Oculi , Humans , Male , Optic Nerve Diseases/pathology , Optic Nerve Diseases/physiopathology , Remission, Spontaneous , Retinal Detachment/pathology , Retinal Detachment/physiopathology , Visual Acuity
3.
Arch Ophthalmol ; 122(10): 1499-506, 2004 Oct.
Article in English | MEDLINE | ID: mdl-15477462

ABSTRACT

OBJECTIVE: To determine whether human immunoglobulin attenuates the toxic effects of Staphylococcus aureus culture supernatant in a rabbit model of endophthalmitis. METHODS: Immunoglobulin binding to products of S aureus strain RN4220 was tested by Western blot analysis using known toxins (beta-hemolysin and toxic shock syndrome toxin-1) and a concentrated culture supernatant containing S aureus exotoxins (pooled toxin). To induce endophthalmitis, pooled toxin was injected into the rabbit vitreous. For immunoglobulin treatment, immunoglobulin and pooled toxin were either mixed and injected simultaneously or immunoglobulin was injected immediately after or 6 hours after pooled toxin injection. Severity of endophthalmitis was graded according to a 9-day course with clinical examination (slitlamp biomicroscopy or indirect ophthalmoscopy) and evaluation of histologic sections. RESULTS: The toxic effects of pooled toxin were markedly reduced when immunoglobulin was mixed with pooled toxin and injected simultaneously. Delayed injection of immunoglobulin diminished its ability to reduce toxicity. Clinical and histologic signs of toxicity were partially attenuated when immunoglobulin was injected immediately after pooled toxin, but only minimal clinically detectable reductions in toxicity were observed when immunoglobulin injection was delayed for 6 hours. CONCLUSION: Pooled human immunoglobulin can attenuate the toxic intravitreal effects of a concentrated culture supernatant containing S aureus exotoxins. Clinical Relevance Immunoglobulin may represent a novel adjuvant in the treatment of bacterial endophthalmitis. To optimize the potential therapeutic benefit, maximizing the mixture of immunoglobulin with bacterial products and early intervention are likely to be important.


Subject(s)
Bacterial Toxins/pharmacology , Endophthalmitis/immunology , Endophthalmitis/therapy , Immunoglobulins/pharmacology , Sphingomyelin Phosphodiesterase/pharmacology , Staphylococcus aureus , Animals , Bacterial Toxins/immunology , Bacterial Toxins/metabolism , Culture Media/metabolism , Disease Models, Animal , Endophthalmitis/pathology , Enterotoxins/immunology , Enterotoxins/metabolism , Enterotoxins/pharmacology , Hemolysin Proteins , Humans , Immunotherapy/methods , Rabbits , Retina/immunology , Retina/pathology , Sphingomyelin Phosphodiesterase/immunology , Sphingomyelin Phosphodiesterase/metabolism , Staphylococcus aureus/metabolism , Superantigens/immunology , Superantigens/metabolism , Superantigens/pharmacology , Vitreous Body/immunology , Vitreous Body/pathology
5.
Am J Ophthalmol ; 135(3): 419-21, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12614778

ABSTRACT

PURPOSE: To report an ocular side effect of topical latanoprost therapy. DESIGN: Single interventional case report. METHODS: A 73-year-old woman on latanoprost for primary open-angle glaucoma developed an iris cyst simulating an iris melanoma. RESULTS: The lesion disappeared over 8 weeks when latanoprost was stopped. CONCLUSIONS: In managing patients with iris-pigmented lesions, the list of medications should be reviewed. If the patient takes latanoprost, a trial off latanoprost is warranted.


Subject(s)
Antihypertensive Agents/adverse effects , Cysts/chemically induced , Iris Diseases/chemically induced , Prostaglandins F, Synthetic/adverse effects , Aged , Cysts/diagnosis , Diagnosis, Differential , Female , Glaucoma, Open-Angle/drug therapy , Humans , Iris Diseases/diagnosis , Iris Neoplasms/diagnosis , Latanoprost , Melanoma/diagnosis
6.
Ophthalmology ; 109(2): 262-6, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11825806

ABSTRACT

PURPOSE: To describe the clinical features of central serous chorioretinopathy (CSC) in women and identify factors predictive of complete recovery, moderate visual loss, and prolonged duration. DESIGN: Retrospective observational case series. PARTICIPANTS: Eighty-four eyes in 78 women with CSC seen in our practices between 1982 and 1999. METHODS: Univariate and multivariate statistical analysis. MAIN OUTCOME MEASURES: Analyses of three outcome parameters: complete recovery (recovery of visual acuity and complete symptom resolution), moderate visual acuity loss (final acuity less than 20/40), and duration of symptoms greater than 5 months. RESULTS: Sixty-two percent (52 of 84) achieved complete recovery over a median of 5 months (range, 2-108 months) and 88% (74 of 84) had a final vision of 20/40 or better. Patients with subretinal precipitates (P = 0.001), single occurrence (P = 0.002), absence of hormone replacement therapy (HRT) (P = 0.01), duration less than 5 months (P = 0.02), or absence of a pigment epithelial detachment (PED) (P = 0.05) were more likely to recover completely. Recurrence (P = 0.03) and lack of subretinal precipitates (P = 0.03) were associated with a final vision less than 20/40. Age older than 50 (P = 0.004) and the presence of a PED (P = 0.02) were associated with duration longer than 5 months. CONCLUSIONS: In women, CSC associated with subretinal precipitates, shorter duration, single occurrence, lack of HRT use, and absence of PED is more likely to resolve completely. CSC occurring in women older than 50 or associated with PED formation is more likely to take longer to resolve.


Subject(s)
Choroid Diseases/diagnosis , Retinal Diseases/diagnosis , Adult , Aged , Choroid Diseases/physiopathology , Exudates and Transudates , Female , Humans , Middle Aged , Remission, Spontaneous , Retinal Diseases/physiopathology , Retrospective Studies , Risk Factors , Vision Disorders/diagnosis , Vision Disorders/physiopathology , Visual Acuity , Women's Health
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