Meredith T A, Wright J D, Gammon J A, Fellner S K, Warshaw B L, Maio M
Arch Ophthalmol. 1984 Apr;102(4):584-7. doi: 10.1001/archopht.1984.01040030462027.
Ocular involvement from primary hyperoxaluria developed in one infant and one teenaged patient. Autopsy procedures in the first case used special histopathologic staining techniques to demonstrate a wider deposition of calcium oxalate crystals within the eye than was previously suspected. Clinical photographs and fluorescein angiograms in the older patient demonstrated a widespread retinal distribution of crystals with a periarterial predilection. This patient also demonstrated a unique acquired black macular lesion.
一名婴儿和一名青少年患者因原发性高草酸尿症出现眼部受累。首例病例的尸检程序采用了特殊的组织病理学染色技术，结果显示眼内草酸钙晶体的沉积范围比之前怀疑的更广。年长患者的临床照片和荧光素血管造影显示晶体在视网膜广泛分布，且偏向于动脉周围。该患者还出现了一种独特的后天性黑色黄斑病变。
