2010
DOI: 10.1007/s10792-009-9337-4
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Successful treatment of choroidal neovascular membrane in retinitis pigmentosa with intravitreal bevacizumab

Abstract: We report a rare association of choroidal neovascularization (CNV) with retinitis pigmentosa and note its resolution by intravitreal injection of the anti-vascular endothelial growth factor (VEGF), bevacizumab. A classic choroidal neovascular membrane was seen in the right eye (RE) of a patient with sector retinitis pigmentosa. Bevacizumab 1.25 mg in 0.05 ml was injected intravitreally. The choroidal neovascular membrane was seen to regress following this single intravitreal bevacizumab injection with formatio… Show more

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Cited by 26 publications
(36 citation statements)
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“…Choroidal neovascular membrane is very rarely associated with RP. To our knowledge, only 8 cases of CNV have been described in the literature [123456]. Seven of them were type 2 CNV, 5 had a subfoveal location, and 2 a juxtafoveal location.…”
Section: Discussionmentioning
confidence: 99%
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“…Choroidal neovascular membrane is very rarely associated with RP. To our knowledge, only 8 cases of CNV have been described in the literature [123456]. Seven of them were type 2 CNV, 5 had a subfoveal location, and 2 a juxtafoveal location.…”
Section: Discussionmentioning
confidence: 99%
“…One case of RP with retinal angiomatous proliferation confirmed by indocyanine green angiogram has been reported in a 60-year-old woman [6]. Based on CNV therapies available at the time of their occurrence, CNVs complicating RP have been treated with laser photocoagulation [1], photodynamic therapy [3], and medical therapy [4, 5]. Intravitreal bevacizumab has been reported to be effective for choroidal neovascular membrane stabilization in patients with RP.…”
Section: Discussionmentioning
confidence: 99%
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“…The association of RP with CNV is even rarer than other dystrophies, and only 5 cases have been reported to date [31,32,33,34]. Retinal pigment epithelium changes and concomitant photoreceptor cell involvement seem to be regularly present in RP, often being associated with choriocapillaris damage [31,32,33]. Our investigation underlines the utility of SD-OCT examination not only for the diagnosis but also for a deeper study of the pathophysiology of RP.…”
Section: Discussionmentioning
confidence: 99%