Wan Yu, Xiao Gege, Yu Ting, Zhang Pei, Hong Jing
Medicine (Baltimore). 2020 Oct 2;99(40):e21892. doi: 10.1097/MD.0000000000021892.
The aim of this study was to investigate the histopathological manifestations of congenital corneal staphyloma accompanied by anterior segment dysgenesis and evaluate the prognosis after penetrating keratoplasty with an ultralarge button graft.We retrospectively studied 8 pediatric patients with large congenital corneal staphylomas in the Department of Ophthalmology of Peking University Third Hospital, China, between September 2014 and December 2018. All patients underwent penetrating keratoplasty with ultralarge button grafts, as well as additional operations according to the abnormality of each eye. Pathological investigations of all samples obtained during penetrating keratoplasty were performed with hematoxylin and eosin staining.The main clinical characteristic of congenital corneal staphyloma was an extremely opaque and ectatic cornea. Histopathological examination showed abnormal corneal epithelia and stroma and an absence of Bowman membrane, Descemet membrane, and the endothelium. Different severities of anterior segment dysgenesis, presenting as various histopathological manifestations, were observed in all cases. Several postoperative complications occurred after penetrating keratoplasty in some of the patients; however, the complications were discovered and treated accordingly in a timely manner. Six patients achieved good visual outcomes and a satisfactory cosmetic appearance after penetrating keratoplasty. One patient eventually lost the transparency of the button because of corneal neovascularization, and 1 patient lost visual function because of retinal detachment.Congenital corneal staphyloma combined with anterior segment dysgenesis can exhibit various manifestations on histopathological examination. Penetrating keratoplasty with an ultralarge button graft seems to be a suitable treatment for congenital corneal staphyloma to obtain good functional and aesthetic prognoses.
本研究旨在探讨伴有前段发育异常的先天性角膜葡萄肿的组织病理学表现,并评估采用超大植片穿透性角膜移植术后的预后。我们回顾性研究了2014年9月至2018年12月期间在中国北京大学第三医院眼科就诊的8例患有大型先天性角膜葡萄肿的儿科患者。所有患者均接受了超大植片穿透性角膜移植术,并根据每只眼睛的异常情况进行了额外的手术。对穿透性角膜移植术中获取的所有样本进行苏木精和伊红染色的病理检查。先天性角膜葡萄肿的主要临床特征是角膜极度混浊和扩张。组织病理学检查显示角膜上皮和基质异常,无Bowman膜、Descemet膜和内皮。所有病例均观察到不同程度的前段发育异常,表现为各种组织病理学表现。部分患者穿透性角膜移植术后出现了几种术后并发症;然而,这些并发症均被及时发现并得到相应治疗。6例患者穿透性角膜移植术后获得了良好的视力结果和满意的外观。1例患者最终因角膜新生血管化导致植片失去透明度,1例患者因视网膜脱离失去视功能。先天性角膜葡萄肿合并前段发育异常在组织病理学检查中可表现出多种表现。采用超大植片穿透性角膜移植术似乎是治疗先天性角膜葡萄肿以获得良好功能和美学预后的合适方法。