IDIOPATHIC POLYPOIDAL CHOROIDAL VASCULOPA THY (IPCV)

Citation
Cw. Spraul et al., IDIOPATHIC POLYPOIDAL CHOROIDAL VASCULOPA THY (IPCV), Klinische Monatsblatter fur Augenheilkunde, 210(6), 1997, pp. 405-406
Citations number
8
Categorie Soggetti
Ophthalmology
Journal title
Klinische Monatsblatter fur Augenheilkunde
ISSN journal
00232165 → ACNP
Volume
210
Issue
6
Year of publication
1997
Pages
405 - 406
Database
ISI
SICI code
0023-2165(1997)210:6<405:IPCVT
Abstract
Background The idiopathic polypoidal choroidal vasculopathy, also know n as ''posterior uveal bleeding syndrome'' or ''multiple recurrent ser osanguineous retinal pigment epithelial detachments in black women'' i s a rare disease entity. A clincopathologic correlation of a patient w ith this disease is presented. Case report A 47-year-old black woman w as evaluated for a decrease of visual acuity in her right eye which ha d occurred over the last 3 months. Ophthalmic examination of her right eye revealed sub-RPE hemorrhage associated with a reddish-orange subr etinal vascular-like lesion. In addition, both eyes displayed a few ch oroidal vascular-like bulbous structures in the superior temporal peri papillary region. The patient developed an extensive choroidal hemorrh age that led eventually to the enucleation of the eye. Conclusion Chor oidal neovascular membranes (CNV) secondary to idiopathic polypoidal c horoidal vasculopathy differs in many aspects from other entities asso ciated with CNV including clinical and fluorescein angiographic featur es, clinical course, and prognosis.