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基质内角膜缘上皮囊肿:先天性和术后性

Intrastromal Keratolimbal Epithelial Cysts: Congenital and Postsurgical.

作者信息

Schoelles Kristina Joana, Auw-Hädrich Claudia, Maier Philip Christian, Reinhard Thomas

机构信息

Klinik für Augenheilkunde, Albert-Ludwigs-Universität Freiburg, Deutschland.

出版信息

Klin Monbl Augenheilkd. 2023 Nov;240(11):1300-1305. doi: 10.1055/a-1682-7300. Epub 2022 Feb 21.

DOI:10.1055/a-1682-7300
PMID:35189648
Abstract

Two very rare cases of intrastromal keratolimbal epithelial cysts are reported. Firstly, an enlarging congenital cyst in a 9-year-old boy, and secondly, a recurrent postsurgical cyst in an 18-year-old female patient. Both cases presented with a limbal cyst, continuing into the corneal stroma as a whitish mass up to the optical axis. The indication for surgery was stabilization of visual acuity in case one and improvement of cosmetic aspects in case two. In the first case, a small part of the cyst was opened at the limbus and the whitish material in the cyst was flushed out. In the second case, anterior lamellar keratectomy over the whole cyst was performed with subsequent application of mitomycin C. Immunohistochemical analysis revealed cytokeratin 19-positive epithelial cells in both cysts. Therefore, an implantation of conjunctival epithelium into the sclera seems to be responsible for the respective keratolimbal cyst. Postsurgically, satisfying cosmetic and functional results were obtained in both cases, with follow-ups of 4 and 9 months. Keratolimbal cysts have rarely been described in the literature. In most cases, a conjunctival epithelial implantation occurs following surgery or trauma and very rarely congenitally. After simple aspiration of the cyst's content, a rapid recurrence is often observed, so that partial or - if possible - complete removal of the anterior cyst wall is recommended, as shown in our cases.

摘要

报告了两例非常罕见的基质内角膜缘上皮囊肿病例。第一例是一名9岁男孩的先天性囊肿逐渐增大,第二例是一名18岁女性患者术后复发囊肿。两例均表现为角膜缘囊肿,作为白色肿物延伸至角膜基质直至视轴。第一例手术指征是稳定视力,第二例是改善外观。第一例中,在角膜缘处打开囊肿的一小部分,冲洗出囊肿内的白色物质。第二例中,对整个囊肿进行前板层角膜切除术,随后应用丝裂霉素C。免疫组织化学分析显示两个囊肿中细胞角蛋白19阳性的上皮细胞。因此,结膜上皮植入巩膜似乎是各自角膜缘囊肿的病因。术后,两例均获得了满意的外观和功能结果,随访时间分别为4个月和9个月。角膜缘囊肿在文献中很少被描述。在大多数情况下,结膜上皮植入发生在手术或创伤后,先天性的情况非常罕见。在简单抽吸囊肿内容物后,经常观察到囊肿迅速复发,因此建议部分或尽可能完全切除囊肿前壁,如我们的病例所示。

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