Hayasaka S, Shoji K, Kanno C, Oura F, Mizuno K
Retina. 1985 Winter-Spring;5(1):30-7.
Three young children showed a similar fundus appearance of sharply defined, yellowish-white, patchy or geographic atrophy of the retina and choroid and visible large choroidal vessels in almost the entire fundus. Fluorescein angiography disclosed atrophy of the retinal pigment epithelium and loss of choriocapillaris. Their visual functions and electrophysiologic findings were also similar. Family A was diagnosed as having diffuse choriocapillaris atrophy with autosomal dominant inheritance; family B, choroideremia with X-linked recessive heredity; and family C, gyrate atrophy of the choroid and retina with hyperornithinemia and autosomal recessive transmission. It became evident that diffuse choriocapillaris atrophy, choroideremia, and gyrate atrophy sometimes show a similar fundus appearance. Fluorescein angiography, serum ornithine levels, and family history were particularly helpful to differentiate these diffuse choroidal atrophies.
三名幼儿眼底表现相似,视网膜和脉络膜呈现边界清晰的黄白色斑片状或地图状萎缩,几乎整个眼底可见粗大的脉络膜血管。荧光素血管造影显示视网膜色素上皮萎缩及脉络膜毛细血管缺失。他们的视觉功能和电生理检查结果也相似。A家系被诊断为常染色体显性遗传的弥漫性脉络膜毛细血管萎缩;B家系为X连锁隐性遗传的脉络膜缺损;C家系为伴有高鸟氨酸血症的常染色体隐性遗传的视网膜脉络膜回旋状萎缩。显然,弥漫性脉络膜毛细血管萎缩、脉络膜缺损和视网膜脉络膜回旋状萎缩有时会呈现相似的眼底表现。荧光素血管造影、血清鸟氨酸水平及家族史对鉴别这些弥漫性脉络膜萎缩尤为有用。