视网膜外膜眼窝畸形的超微结构细节。

IF 2.1 4区 医学 Q2 OPHTHALMOLOGY Ophthalmologica Pub Date : 2024-01-01 Epub Date: 2023-12-23 DOI:10.1159/000535539
Denise Vogt, Ricarda G Schumann, Yulia Zaytseva, Caroline Wiecha, Armin Wolf, Siegfried G Priglinger, Julian E Klaas
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引用次数: 0

摘要

导言:描述特发性视网膜外膜(ERM)眼窝裂孔与黄斑假洞(MPH)和片状黄斑洞(LMH)相比,玻璃体-黄斑界面(VMI)的差异:我们分析了在标准玻璃体旁切除术(PPV)中从16名ERM眼窝裂孔患者(6眼)、MPH患者(5眼)和LMH患者(5眼)的眼球中切除的视网膜上皮和内缘膜标本。根据新引入的光学相干断层扫描(OCT)术语对这三种实体进行了分类。透射电子显微镜(TEM)用于描述超微结构特征:结果:我们在分析的所有样本中都发现了纤维细胞性视网膜后组织。然而,各组间 VMI 的细胞和胶原成分各不相同。与 MPH 相比,ERM 眼窝畸形眼的特点是细胞数量较多、多层膜和玻璃体胶原厚股,其中包埋着肌成纤维细胞等主要细胞类型。患有 MPH 的眼球也显示肌成纤维细胞占多数,但这些细胞直接位于 ILM 上,细胞与 ILM 之间没有胶原蛋白。LMH患者的眼球表现为厚而多层的视网膜上皮增生,主要由非牵拉性神经胶质细胞组成,与OCT上的低密度视网膜上皮增生相对应。与LMH相比,有ERM眼窝畸形和MPH的眼睛在后视紫质状态方面更有可能存在不完全的PVD:ERM foveoschis和MPH眼球中的ractional ERM在超微结构上存在差异。主要区别在于玻璃体胶原的数量和地形分布。尽管这两种病变的视网膜外细胞类型都主要是肌成纤维细胞。这凸显了在发病机制和手术剥离程序方面将 ERM 眼窝裂孔与 MPH 和 LMH 区分开来的重要性。
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Ultrastructural Details of Epiretinal Membrane Foveoschisis.

Introduction: The aim of this study was to describe differences in the vitreomacular interface (VMI) in idiopathic epiretinal membrane (ERM) foveoschisis compared to macular pseudohole (MPH) and lamellar macular hole (LMH).

Methods: We analysed surgically excised epiretinal material and internal limiting membrane (ILM) specimens obtained from 16 eyes of 16 patients with ERM foveoschisis (6 eyes), MPH (5 eyes), and LMH (5 eyes) during standard pars plana vitrectomy (PPV) with membrane peeling. The three entities were classified according to the newly introduced optical coherence tomography (OCT) terminology. Transmission electron microscopy (TEM) was used to describe the ultrastructural features.

Results: We found fibrocellular epiretinal tissues in all samples analysed. However, the cell and collagen composition of the VMI differed between groups. Eyes with ERM foveoschisis were characterized by a higher number of cells, multilayered membranes, and thick strands of vitreous collagen embedding the major cell types of myofibroblasts compared to MPH. Eyes with MPH also showed a predominance of myofibroblasts, but these were located directly on the ILM with no collagen between the cells and the ILM. Eyes with LMH showed a thick, multilayered epiretinal proliferation consisting mainly of non-tractional glial cells, corresponding to hypodense epiretinal proliferation on OCT. Eyes with ERM foveoschisis and MPH were more likely to have incomplete PVD compared to LMH in terms of posterior hyaloid status.

Discussion/conclusion: Tractional ERMs in eyes with ERM foveoschisis and MPH differ in their ultrastructure. The main difference is in the amount and topographical distribution of vitreous collagen. However, the epiretinal cell types are predominantly myofibroblasts in both entities. This highlights the importance of distinguishing ERM foveoschisis from both MPH and LMH in terms of pathogenesis and surgical peeling procedures.

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来源期刊
Ophthalmologica
Ophthalmologica 医学-眼科学
CiteScore
5.10
自引率
3.80%
发文量
39
审稿时长
3 months
期刊介绍: Published since 1899, ''Ophthalmologica'' has become a frequently cited guide to international work in clinical and experimental ophthalmology. It contains a selection of patient-oriented contributions covering the etiology of eye diseases, diagnostic techniques, and advances in medical and surgical treatment. Straightforward, factual reporting provides both interesting and useful reading. In addition to original papers, ''Ophthalmologica'' features regularly timely reviews in an effort to keep the reader well informed and updated. The large international circulation of this journal reflects its importance.
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