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Arch Ophthalmol. 2002;120:502-508.

	Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

Idiopathic polypoidal choroidal vasculopathy (IPCV), a peculiar hemorrhagic disorder of the macula involving serosanguineous detachments of the retinal pigment epithelium (RPE) and neurosensory retina, was first described by Yannuzzi¹ at a meeting of the Macula Society in 1982. At the American Academy of Ophthalmology in 1984, Kleiner and coworkers² described 7 patients with varying degrees of visual loss secondary to multiple recurrent hemorrhages or serous fluid beneath the RPE and neurosensory retina in the posterior fundus, and coined the phrase posterior uveal bleeding syndrome for this condition. In 1985, Stern and coworkers³ published the first report on "multiple recurrent serosanguineous RPE detachments" in 3 middle-aged black women. In his 1987 atlas, Gass⁴ described 3 black women with subretinal bleeding from multicentric neovascular networks with orange sub-RPE plaques or nodules in the peripapillary region.

Several additional reports and case series^5-11 and 2 clinicopathologic studies^12-13 have been published. The previously published pathologic . . . [Full Text of this Article]

Report of a Case


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Corresponding author and reprints: Robert H. Rosa, Jr, MD, Division of Ophthalmology, Scott and White Clinic, 2401 S 31st St, Temple, TX 76508 (e-mail: rrosa@swmail.sw.org).

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