Nagpal K C, Patrianakos D, Asdourian G K, Goldberg M F, Rabb M, Jampol L
Am J Ophthalmol. 1975 Nov;80(5):885-92. doi: 10.1016/0002-9394(75)90285-8.
Of 45 patients with proliferative sickle retinopathy in stages III, IV, and V, nine patients (eight with hemoglobin SC disease, one with sickle cell thalassemia) showed spontaneous regression (autoinfarction) of retinal sea fans. One mechanism involved in autoinfarction of neovascular tissue is progressive, centripetal retraction of the anterior vascular arcade of the peripheral retina. In addition, vitreous traction on feeder vessels may result in sluggish blood flow and occlusion of these vessels, or may tear the sea fan completely away from its feeder vessels. In view of the many incidences of vitreous hemorrhages that occur in patients with proliferative retinopathy, however, we recommend treatment of neovascularization rather than prolonged observation.
在45例处于III、IV和V期的增殖性镰状视网膜病变患者中,9例患者(8例血红蛋白SC病,1例镰状细胞地中海贫血)的视网膜海扇出现自发性消退(自身梗死)。新生血管组织自身梗死所涉及的一种机制是周边视网膜前血管弓向心性渐进性收缩。此外,玻璃体对供血血管的牵拉可能导致血流缓慢和这些血管闭塞,或者可能将海扇完全从其供血血管上撕裂。然而,鉴于增殖性视网膜病变患者中发生玻璃体出血的情况很多,我们建议对新生血管进行治疗,而不是长期观察。