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Bilateral choroidal osteomas with polypoidal choroidal vasculopathy. | LitMetric

Bilateral choroidal osteomas with polypoidal choroidal vasculopathy.

Retin Cases Brief Rep

From the Vitreous, Retina, Macula Consultants of New York, and the LuEsther T. Mertz Retina Research Laboratory, Manhattan Eye, Ear, and Throat Hospital, New York, New York.

Published: November 2014

Background: A choroidal osteoma is a benign osseous tumor typically arising in the juxtapapillary or peripapillary area. The major cause of visual loss is secondary to the development of a subretinal neovascular membrane. The pattern of neovascularization that develops with osteomas has been typically described as classic choroidal neovascularization (CNV).

Methods: Interventional case report.

Results: A case of bilateral polypoidal choroidal neovascularization (PCV) occurring with bilateral choroidal osteomas is described in a 55-year-old Japanese woman. To our knowledge, this variant form of vasogenesis has not previously been described in association with this tumor. Clinical, angiographic, and optical coherence tomographic features are discussed. Subretinal hemorrhage in the left eye from polypoidal neovascularization in the macula was successfully treated with photodynamic therapy.

Conclusions: The association between choroidal osteoma and PCV may have a better prognosis than that with classic CNV. Indocyanine green angiography is a useful tool in characterizing the nature of the neovascularization.

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Source
http://dx.doi.org/10.1097/ICB.0b013e318159e7e9DOI Listing

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