Department of Ophthalmology, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Jpn J Ophthalmol. 2010 Jan;54(1):66-73. doi: 10.1007/s10384-009-0770-8. Epub 2010 Feb 12.
To clarify the relationship between clinical symptoms and histological status in patients with ocular cicatricial pemphigoid (OCP) and Stevens-Johnson syndrome (SJS).
Clinical symptoms of four OCP and eight SJS patients in the chronic phase were scored with our recently proposed grading system. The histological status of the pannus tissue removed from the corneal surface during surgery was investigated using immunohistological techniques.
All participants showed total loss of the palisades of Vogt and conjunctivalization of the entire corneal surface. All pannus tissues expressed the conjunctival epithelium marker CK4/13. The pannus tissue in clinically keratinized SJS expressed skin epidermal major cytokeratins, but the tissues of nonkeratinized SJS did not.
Clinical observation and the use of our recently proposed grading system agreed with the immunohistological status with respect to keratinization, cell proliferation, and corneal/conjunctival cell typing. These findings facilitate our understanding of the pathogenesis of OCP and SJS, and will hopefully contribute to the development of future treatment strategies and improve predictions of the postoperative prognosis of ocular surface reconstruction in patients with OCP and SJS.
阐明眼瘢痕性类天疱疮(OCP)和 Stevens-Johnson 综合征(SJS)患者的临床症状与组织学状态之间的关系。
使用我们最近提出的分级系统对处于慢性期的 4 名 OCP 和 8 名 SJS 患者的临床症状进行评分。通过免疫组织化学技术研究从手术中切除的角膜表面的假性胬肉组织的组织学状态。
所有参与者均表现为 Vogt 氏嵴完全丧失和整个角膜表面的结膜化。所有假性胬肉组织均表达结膜上皮标志物 CK4/13。临床上角化的 SJS 的假性胬肉组织表达皮肤表皮主要细胞角蛋白,但非角化的 SJS 的组织则不表达。
临床观察和使用我们最近提出的分级系统与免疫组织学状态在角化、细胞增殖和角膜/结膜细胞类型方面一致。这些发现有助于我们了解 OCP 和 SJS 的发病机制,并有望为未来的治疗策略的发展做出贡献,并改善 OCP 和 SJS 患者眼表面重建术后预后的预测。