Samimi Sépideh, Leger François, Touboul David, Colin Joseph
Ophthalmology and Pathology Departments, Hospital Pellegrin, Bordeaux, France.
J Cataract Refract Surg. 2007 Feb;33(2):247-53. doi: 10.1016/j.jcrs.2006.08.059.
To evaluate histopathological changes induced in keratoconic corneas after implantation of Intacs intracorneal ring segments (Addition Technology, Inc.).
Departments of Ophthalmology and Pathology, Hospital Pellegrin, Bordeaux, France.
This retrospective study included 8 keratoconic, contact-lens-intolerant eyes of 8 patients who had penetrating keratoplasty (PKP) after removal of Intacs inserts because of a poor refractive outcome or insert extrusion. Light microscopy was performed on all specimens after conventional staining. Immunohistochemistry was performed to identify cell types located next to the tunnel using AE1/AE3 cytokeratins, CD34, vimentin, collagen IV, and alpha-smooth muscle actin monoclonal antibodies.
Conventional histology showed hypoplasia of the epithelium immediately surrounding the channel. There was no evidence of an inflammatory response or foreign-body granuloma. Keratocyte density was decreased above and below the tunnel, and collagen IV synthesis was seen in the scar area. All samples stained negatively with alpha-smooth muscle actin, indicating that myofibroblasts were not present. These changes were no longer visible when PKP was performed more than 6 months after Intacs explantation.
Intacs induced keratocyte apoptosis, probably through a switch to a collagenous synthetic phenotype. Although histological changes seem to be entirely reversible after implant removal, longer follow-up is necessary to determine whether they accelerate corneal thinning and keratoconus progression via apoptosis and release of metalloprotease.
评估植入Intacs角膜内环片(Addition Technology公司)后圆锥角膜的组织病理学变化。
法国波尔多市佩勒格林医院眼科与病理科。
本回顾性研究纳入8例患者的8只圆锥角膜且不耐受接触镜的眼睛,这些患者因屈光结果不佳或内环片脱出在取出Intacs插入物后接受了穿透性角膜移植术(PKP)。所有标本经传统染色后进行光学显微镜检查。使用AE1/AE3细胞角蛋白、CD34、波形蛋白、IV型胶原和α-平滑肌肌动蛋白单克隆抗体进行免疫组织化学检查,以识别隧道旁的细胞类型。
传统组织学显示紧邻通道的上皮发育不全。没有炎症反应或异物肉芽肿的证据。隧道上方和下方的角膜细胞密度降低,在瘢痕区域可见IV型胶原合成。所有样本α-平滑肌肌动蛋白染色均为阴性,表明不存在肌成纤维细胞。在Intacs取出后6个月以上进行PKP时,这些变化不再可见。
Intacs可能通过转变为胶原合成表型诱导角膜细胞凋亡。尽管植入物取出后组织学变化似乎完全可逆,但需要更长时间的随访来确定它们是否通过细胞凋亡和金属蛋白酶释放加速角膜变薄和圆锥角膜进展。