IDIOPATHIC POLYPOIDAL CHOROIDAL VASCULOPATHY (IPCV)
IDIOPATHIC POLYPOIDAL CHOROIDAL VASCULOPATHY (IPCV)
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DOI：
10.1097/iae.0b013e31823f992a
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发表时间：
2012-02
期刊：
影响因子：
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通讯作者：
L. Yannuzzi;J. Sorenson;R. Spaide;B. Lipson
中科院分区：
文献类型：
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作者：
L. Yannuzzi;J. Sorenson;R. Spaide;B. Lipson
摘要11例40 ~ 71岁的脉络膜血管病变导致出血性和渗出性黄斑变性。患者有特殊的息肉状视网膜下血管病变，伴有视网膜色素上皮的浆液性和出血性脱髓鞘。这种黄斑疾病，我们称之为特发性息肉状脉络膜血管病（IPCV），似乎代表了一种独特的实体，其在临床上和人口统计学上不同于年龄相关性黄斑变性（AMD）和其他与视网膜下新生血管相关的黄斑疾病。认识到这种情况是很重要的，因为它可能有特定的风险因素，自然过程和管理考虑不同于年龄相关性黄斑变性。
Abstract Eleven patients, 40 to 71 years old, had a choroidal vasculopathy that led to hemorrhagic and exudative macular degeneration. The patients had peculiar polypoidal, subretinal, vascular lesions associated with serous and hemorrhagic detachments of the retinal pigment epithelium. This macular disorder, which we have named idiopathic polypoidal choroidal vasculopathy (IPCV), appears to represent a distinct entity that differs clinically and demograph-ically from age-related macular degeneration (AMD) and other macular diseases associated with subretinal neovascularization. Recognition of this condition is important because it may have specific risk factors, natural course, and management considerations that differ from those of age-related macular degeneration.