Foos R Y
Albrecht Von Graefes Arch Klin Exp Ophthalmol. 1975;195(2):87-100. doi: 10.1007/BF00417112.
A pathologic analysis of 19 cases of acute retrolental fibroplasia in autopsy eyes from paranatal infants is presented. The clinical profile of these subjects showed no clear-cut maternal factors. Infant factors included systemic congenital anomalies (14 cases); ocular congenital anomalies (1); birth weight--less than 1500 grams (12), more than 2000 grams (4); neonatal complications--"respiratory distress" (8), "apneic spells" (7), Erythroblastosis fetalis (3); oxygen therapy of varying amounts (14); periodic elevations of arterial oxygen (7); and varying survival times (intrauterine death, one case; less then 48 extrauterine hours, 9 cases). Considering all cases, the lesions showed a progressive pattern--beginning with proliferation of primitive vascular mesenchyme in vanguard of advancing vasculature (four cases), formation of intraretinal band of endothelial cells in rear guard (10 cases), and finally, extraretinal neovascularization from rear guard zone (five cases).
本文呈现了对19例围产期婴儿尸检眼中急性晶状体后纤维增生症的病理分析。这些受试者的临床特征未显示出明确的母体因素。婴儿因素包括全身性先天性异常(14例);眼部先天性异常(1例);出生体重——小于1500克(12例),大于2000克(4例);新生儿并发症——“呼吸窘迫”(8例),“呼吸暂停发作”(7例),胎儿成红细胞增多症(3例);不同剂量的氧疗(14例);动脉血氧的周期性升高(7例);以及不同的存活时间(宫内死亡,1例;宫外存活少于48小时,9例)。综合所有病例,病变呈现出一种渐进模式——始于前进血管前沿的原始血管间充质增生(4例),后卫区视网膜内内皮细胞带形成(10例),最后是后卫区视网膜外新生血管形成(5例)。