PLACOID PIGMENT EPITHELIOPATHY AND HARADAS DISEASE
PLACOID PIGMENT EPITHELIOPATHY AND HARADAS DISEASE
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DOI：
10.1136/bjo.62.9.609
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发表时间：
1978-01-01
影响因子：
4.1
通讯作者：
HAMILTON, AM
中科院分区：
文献类型：
--
作者：
WRIGHT, BE;BIRD, AC;HAMILTON, AM
描述了26例急性双侧多灶性色素上皮病患者。在7例患者中，疾病类型与急性后部多灶性片状色素上皮病难以区分，而在8例患者中，与原田病难以区分。在另外9例病例中，色素上皮疾病与类似原田病的视网膜浆液性脱离相关，但无全身症状;几天内自发消退，无复发。另外1例患者最初有短暂的疾病伴脱离，但随后出现严重复发，最后1例患者的1只眼睛出现浆液性脱离，而另一只眼睛没有。当被视为一个整体时，这些患者似乎代表了一个连续的疾病谱，使得很难定义一种疾病与另一种疾病之间的界限。强调了仅根据形态学鉴别疾病的困难。
Patients (26) were described who suffered from acute bilateral multifocal pigment epithelial disease. In 7 the pattern of disease was indistinguishable from acute posterior multifocal placoid pigment epitheliopathy, while in 8 it was indistinguishable from Harada''s disease. In a further 9 cases the pigment epithelial disease was associated with serous detachment of the retina simulating Harada''s disease but without systemic symptoms; spontaneous resolution occurred within a few days, and there was no recurrence. One additional case had short-lived disease with detachment initially, but this was followed by severe recurrence, and the last patient had serous detachment in 1 eye but not the other. When seen as a whole these patients appeared to represent a continuous spectrum of disease making it difficult to define boundaries between one condition and another. The difficulties in distinguishing diseases according to morphology alone were emphasized.