使用激光共聚焦扫描显微镜和相应的组织学方法,对比眼睑边缘真皮乳头和睑板腺小体的表现。

IF 0.8 4区 医学 Q4 OPHTHALMOLOGY Klinische Monatsblatter fur Augenheilkunde Pub Date : 2024-11-01 Epub Date: 2024-05-27 DOI:10.1055/a-2302-7526
A Csorba, L Imre, I Szalai, O Lukáts, E Fodor, A Szabó, Z Z Nagy
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引用次数: 0

摘要

背景:许多研究使用共焦激光扫描显微镜(CLSM)对眼睑边缘进行了研究,结果表明受检结构的形态发生了改变,并推测这些结构是睑板腺。然而,最近的数据证实,这些结构是真皮表皮交界处的真皮乳头的横截面。本研究旨在介绍共聚焦激光扫描显微镜检查到的睑板腺尖锐湿疣与真皮乳头的形态外观对比,并揭示特定组织学切片的相应模式:使用共聚焦激光扫描显微镜设备对 20 名健康患者的眼睑边缘进行活体检查。收集了 22 名经手术治疗的眼睑外翻患者的 22 个全厚眼睑楔形样本,其中 11 个新鲜切除样本在切口表面用 CLSM 进行了活体成像,11 个眼睑进行了常规组织学制备。就面积、最长和最短直径以及深度和密度而言,CLSM 图像上的代表结构与组织学切片上的睑板腺针孔进行了比较:结果:在活体 CLSM 图像上,可以识别睑板腺孔口、表皮细胞和真皮结缔组织,后者在真皮乳头的横截面上被表皮基底细胞包围,形成反射环状结构。这些结构的所有形态参数都与在组织切片上测量到的睑板腺小体不同。与此相反,切口表面的 CLSM 图像显示了与组织学图像中的睑板腺针状突起具有相同形态的针状突起单位,而且相应参数之间没有统计学意义上的显著差异:结论:睑板腺棘突的形态外观与之前在CLSM图像上被推测为睑板腺的结构不同。常用的活体 CLSM 无法对睑板腺进行活体成像。
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Presentation of Meibomian Acini Compared to Dermal Papillae of the Eyelid Margin, Using Confocal Laser Scanning Microscopy and Corresponding Histology.

Background: Numerous studies have investigated the eyelid margin using confocal laser scanning microscopy (CLSM) and have presented morphological alterations of the examined structures, which were presumed to be Meibomian acini. However, recent data confirm that these structures are the cross-sections of dermal papillae of the dermoepidermal junction. This study aims to present the morphological appearance of Meibomian acini examined by confocal laser scanning microscopy in comparison to dermal papillae, and to reveal the corresponding patterns with specific histological sections.

Methods and material: Twenty healthy patients were examined with a CLSM device in vivo at the marginal edge of the eyelid. Twenty-two samples of full-thickness eyelid wedges from 22 patients treated surgically with ectropion were collected, of which 11 freshly excised samples were imaged on the incision surface with CLSM ex vivo and 11 eyelids underwent conventional histological preparation. The represented structures on CLSM images were compared to Meibomian acini on histological sections in terms of area, longest and shortest diameter, as well as depth and density.

Results: On in vivo CLSM images, Meibomian orifices, epidermal cells, and dermal connective tissue could be identified, the latter in a cross-sectional view of the dermal papillae surrounded by basal cells of the epidermis, forming reflective ring-like structures. All morphological parameters of these structures differed from Meibomian acini measured on histological sections. In contrast, the CLSM images of the incision surface showed acinar units with the same morphology as the Meibomian acini seen in the histological images and no statistically significant difference was found between the corresponding parameters.

Conclusion: The morphological appearance of Meibomian acini differs from the structures that were previously presumed as Meibomian glands on CLSM images. In vivo imaging of Meibomian glands by commonly used in vivo CLSM cannot be performed.

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