Fluorescein Angiography in Patients With Posterior Uveitis

Listhaus, Alan D.; Freeman, William R.

doi:10.1097/00004397-199030040-00021

Cited by 7 publications

(2 citation statements)

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“…In 50% of cases, they are associated with subretinal pooling of dye. These angiographic patterns correspond to papillitis, choroiditis and serous retinal detachment respectively [6], [7]. The diffuse choroidal inflammation that is present during the acute stage generally spares the choriocapilaris [8] but is associated with medium sized vessel inflammation.…”

Section: Discussionmentioning

confidence: 99%

Fluorescein fundus angiographic findings in Vogt–Koyanagi–Harada syndrome

et al. 2007

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Section: Discussionmentioning

confidence: 99%

Fluorescein fundus angiographic findings in Vogt–Koyanagi–Harada syndrome

et al. 2007

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“…Intraocular inflammation is associated with vascular alterations and very often include disturbances of the retinal and/or choroidal circulations. [12]…”

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confidence: 99%

Indocyanine green angiography in posterior uveitis

Agrawal

Biswas

Gunasekaran

2013

Indian J Ophthalmol

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Literature review for indocyanine green angiography and evaluate the role of indocyanine green angiogram (ICGA) in patients with posterior uveitis seen at a tertiary referral eye care centre. Detailed review of the literature on ICGA was performed. Retrospective review of medical records of patients with posterior uveitis and dual fundus and ICGA was done after institutional board approval. Eighteen patients (26 eyes) had serpiginous choroiditis out of which 12 patients had active choroiditis and six patients had healed choroiditis, six patients (12 eyes) had ampiginous choroiditis, six patients (12 eyes) had acute multifocal posterior placoid pigment epitheliopathy, eight patients (10 eyes) had multifocal choroiditis, four patients (eight eyes) had presumed ocular histoplasmosis syndrome, four patients (eight eyes) had presumed tuberculous choroiditis, two patients (four eyes) had multiple evanescent white dot syndrome and two patients (four eyes) had Vogt Koyanagi Harada (VKH) syndrome. The most characteristic feature noted on ICGA was the presence of different patterns of hypofluorescent dark spots, which were present at different stages of the angiogram. ICGA provides the clinician with a powerful adjunctive tool in choroidal inflammatory disorders. It is not meant to replace already proven modalities such as the fluorescein angiography, but it can provide additional information that is useful in establishing a more definitive diagnosis in inflammatory chorioretinal diseases associated with multiple spots. It still needs to be determined if ICGA can prove to be a follow up parameter to evaluate disease progression.

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