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关于跗骨内角质囊肿发病机制的组织病理学研究。

Histopathological Study on the Proposed Pathogenesis of Intratarsal Keratinous Cysts.

机构信息

Departments of Ophthalmology.

Pathology, University of Ottawa, The Ottawa Hospital, Ottawa, Ontario, Canada.

出版信息

Ophthalmic Plast Reconstr Surg. 2019 Jul/Aug;35(4):365-368. doi: 10.1097/IOP.0000000000001271.

Abstract

PURPOSE

Intratarsal keratinous cysts (IKCs) are a recently described entity that is frequently misdiagnosed clinically as chalazia and mislabeled in the literature as "intratarsal epidermal inclusion cysts" or "epidermoid cysts." It is important to accurately diagnose IKCs and distinguish them from chalazia because IKCs require a complete surgical excision and can exhibit multiple recurrences following curettage. The authors performed a retrospective case series to further elucidate the pathogenesis of IKCs and to determine the diagnostically optimal panel of stains for diagnosis.

METHODS

A study group of 8 specimens of IKCs and control specimens of epidermal inclusion cysts were obtained from their pathology laboratories. The authors compared the histological and immunohistochemical profile of IKCs and epidermal inclusion cysts by staining sections from each specimen with hematoxylin and eosin, periodic acid-Schiff, Masson trichrome, cytokeratin 5, cytokeratin 17, carcinoembryonic antigen, and epithelial membrane antigen. The immunoreactivity data were then analyzed using a 2-tailed Mann-Whitney test, assuming a nonparametric population (p < 0.05 is significant).

RESULTS

Histopathologically, IKCs are embedded in the tarsus lined by stratified squamous epithelium with an inner undulating cuticle filled with a compact keratinous-appearing material. The authors demonstrate that IKCs develop progressively from dilated meibomian ducts to the formation of complete cysts with their markers. The most valuable immunochemical stains to diagnose IKC were cytokeratin 17, carcinoembryonic antigen, and epithelial membrane antigen (p < 0.05 with each).

CONCLUSIONS

These findings provide a better understanding of the pathogenesis and the immunohistochemical findings of this relatively new entity allowing for more appropriate diagnosis of IKCs aiming to reduce future complications from their management.

摘要

目的

内睑板角蛋白性囊肿(IKC)是一种最近描述的实体,临床上常被误诊为霰粒肿,并在文献中被错误地标记为“内睑板表皮包涵囊肿”或“表皮样囊肿”。准确诊断 IKC 并将其与霰粒肿区分开来非常重要,因为 IKC 需要完整的手术切除,并且在刮除后可能会多次复发。作者进行了一项回顾性病例系列研究,以进一步阐明 IKC 的发病机制,并确定用于诊断的最佳诊断染色面板。

方法

从他们的病理实验室获得了 8 个 IKC 标本和表皮包涵囊肿的对照标本的研究组。作者通过对每个标本的切片进行苏木精和伊红、过碘酸-希夫、马松三色、细胞角蛋白 5、细胞角蛋白 17、癌胚抗原和上皮膜抗原染色,比较了 IKC 和表皮包涵囊肿的组织学和免疫组织化学特征。然后使用双尾曼-惠特尼检验分析免疫反应性数据,假设为非参数群体(p<0.05 为显著)。

结果

组织病理学上,IKC 嵌入由复层鳞状上皮衬里的睑板,内有波浪状的外皮,充满致密的角化样物质。作者表明,IKC 从扩张的睑板腺逐渐发展为形成完整的囊肿,同时保留其标志物。诊断 IKC 最有价值的免疫化学染色是细胞角蛋白 17、癌胚抗原和上皮膜抗原(每种染色均有统计学意义,p<0.05)。

结论

这些发现提供了对这种相对较新实体的发病机制和免疫组织化学发现的更好理解,从而可以更准确地诊断 IKC,旨在减少其治疗后的并发症。

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