Fishman G A, Baskin M, Jednock N
Ann Ophthalmol. 1977 Jan;9(1):36-6.
Acute posterior multifocal placoid pigment epitheliopathy (APMPPE) is a disorder of the fundus frequently characterized by sudden onset of bilateral, marked visual loss associated with yellowish-white, ill-defined placoid lesions of the retina. Most cases show a rapid resolution with restoration of vision to normal or near-normal levels. We evaluated an 11-year-old boy with presumed APMPPE who showed a mononuclear cell pleocytosis on spinal fluid examination.
急性后极部多灶性鳞状色素上皮病变（APMPPE）是一种眼底疾病，其特征通常为双侧突然出现明显视力丧失，并伴有视网膜黄白色、边界不清的鳞状病变。大多数病例视力迅速恢复，达到正常或接近正常水平。我们评估了一名11岁疑似患有APMPPE的男孩，其脑脊液检查显示单核细胞增多。
