Abstract:VKH disease presenting with a bilateral increased IOP mostly occurs in older women. The strikingly decreased visual acuity associated with mild to moderate increased IOP is a clue to the diagnosis. The increased IOP responded well to corticosteroids but not to anti-glaucoma treatment.
“…Inflammatory uveal effusions, such as those secondary to posterior scleritis and VKH syndrome are effectively managed with systemic corticosteroids and steroid-sparing drugs such as methotrexate and azathioprine. 7 Drug-induced uveal effusions gradually resolve on cessation of the causative drug in consultation with the patient's physician. Topical corticosteroids help reduce ciliary inflammation in these cases.…”
Uveal effusion is a complex and poorly understood clinical entity with significant visual morbidity and is caused by a range of ocular and systemic diseases. Effective management is critically dependent on the underlying cause.
“…Inflammatory uveal effusions, such as those secondary to posterior scleritis and VKH syndrome are effectively managed with systemic corticosteroids and steroid-sparing drugs such as methotrexate and azathioprine. 7 Drug-induced uveal effusions gradually resolve on cessation of the causative drug in consultation with the patient's physician. Topical corticosteroids help reduce ciliary inflammation in these cases.…”
Uveal effusion is a complex and poorly understood clinical entity with significant visual morbidity and is caused by a range of ocular and systemic diseases. Effective management is critically dependent on the underlying cause.
“…Mansouri and Ravinet reported that iridoplasty was successful in the treatment of a uveitic eye with acute angle closure which was resistant to medical treatment and repeated laser iridotomies (Yang et al, 2011). Besides this isolated report, there is little additional evidence for the efficacy of iridoplasty in the treatment of angle closure in eyes with uveitis, and it is often not possible to mechanically widen the angle with laser burns to the iris in uveitic eyes (Kok and Barton, 2002).…”
Section: Specific Treatment For Angle Closurementioning
confidence: 95%
“…Detachment of the ciliary body occurs in eyes with severe ocular inflammation and has been associated with posterior scleritis (Heinz et al, 2013), Vogt-KayanagiHarada disease (Kishi et al, 1996;Yang et al, 2011;Yao et al, 2013), pars planitis, and uveal effusion syndrome (Saari, 1976). These patients can present with an acute increase in IOP (Kishi et al, 1996;Yamamura et al, 2008;Yang et al, 2011;Yao et al, 2013) and are easily misdiagnosed as acute primary angle closure.…”
Section: Anterior Displacement Of the Iris-lens Diaphragmmentioning
confidence: 97%
“…These patients can present with an acute increase in IOP (Kishi et al, 1996;Yamamura et al, 2008;Yang et al, 2011;Yao et al, 2013) and are easily misdiagnosed as acute primary angle closure. Secondary causes of acute angle closure should be considered in the context of younger patients, bilateral simultaneous ocular involvement in the absence of pupillary changes, and severely decreased vision which is inconsistent with only moderately elevated IOP (Yang et al, 2011). A comprehensive examination of the posterior segment may reveal other signs of ocular inflammation, including disc swelling, exudative retinal detachment, and choroiditis (Yang et al, 2011).…”
Section: Anterior Displacement Of the Iris-lens Diaphragmmentioning
confidence: 97%
“…Secondary causes of acute angle closure should be considered in the context of younger patients, bilateral simultaneous ocular involvement in the absence of pupillary changes, and severely decreased vision which is inconsistent with only moderately elevated IOP (Yang et al, 2011). A comprehensive examination of the posterior segment may reveal other signs of ocular inflammation, including disc swelling, exudative retinal detachment, and choroiditis (Yang et al, 2011). Topiramate ingestion is also associated with ciliary body detachment, choroidal effusions, and anterior rotation of the ciliary processes (Etminan et al, 2012;Kamal et al, 2014;Senthil et al, 2010).…”
Section: Anterior Displacement Of the Iris-lens Diaphragmmentioning
A Korean American woman in her early 60s was referred for evaluation of bilateral acuteangle closure and retinal detachments. She had emmetropia, and her ocular and medical history were unremarkable. Over the preceding few days, she noticed worsening blurry vision with redness in both eyes associated with headaches, nausea, and severe tinnitus. On presentation, her best-corrected visual acuity was 20/200 OD and 20/400 OS. Intraocular pressure was 45 mm Hg OU. Pupils were 4 mm and minimally reactive. There was 1+ conjunctival injection, diffuse corneal edema with Descemet folds, and the anterior chamber was shallow in both eyes. After the administration of multiple rounds of topical and oral medications, her intraocular pressure improved to 18 mm Hg OD and 19 mm Hg OS. A dilated fundus examination revealed tilted discs, serous retinal detachments, and multiple yellow, depigmented chorioretinal spots throughout the posterior pole in both eyes. B-scan ultrasonography showed shallow retinal detachments, choroidal thickening, and extensive, shallow choroidal detachments extending anteriorly in both eyes (Figure 1A). A-scan ultrasonography showed normal axial length of 22 mm OU. Optical coherence tomography indicated subretinal fluid and enhanced depth imaging demonstrated significant choroidal thickening in both eyes (Figure 1B). Fluorescein angiography revealed pinpoint hyperfluorescence with leakage. Indocyanine green angiography showed diffuse leakage throughout the posterior pole in both eyes.
Diagnosis
Vogt-Koyanagi-Harada disease
What to Do Next
C. Request a workup for infectious causes and start prednisone therapy
Discussion
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