King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia; Department of Ophthalmology, King Saud University School of Medicine, Riyadh, Saudi Arabia.
Department of Ophthalmology and Visual Sciences and, University of Iowa Carver College of Medicine, Iowa City, Iowa.
Ophthalmol Glaucoma. 2022 Jul-Aug;5(4):396-401. doi: 10.1016/j.ogla.2022.01.003. Epub 2022 Feb 4.
This series describes the immunopathologic features of posterior embryotoxon (PE) and demonstrates that it is not an anterior displaced Schwalbe's line as commonly described, but a peripheral corneal stromal nub variable in location with abnormal extracellular matrix.
Case series.
Archived specimens from patients with PE.
Sections from archived formalin-fixed, paraffin-embedded specimens (n = 9; 7 autopsy and 2 trabeculectomy specimens) were examined by light microscopy. Immunohistochemistry was performed on 5 specimens to characterize the extracellular matrix composition of PE.
Posterior embryotoxon appeared as nubs of whorled collagen extending from the corneal stroma, lined in some instances, by Descemet membrane. These nubs were located anterior to Schwalbe's line (n = 4), posteriorly (n = 1), partially embedded in the trabecular meshwork (n = 1), or at Schwalbe's line (n = 2). Qualitatively, collagen I labeling of the PE stroma was similar or weaker than the corneal stroma, whereas collagen III staining was focal and slightly more intense compared with the corneal stroma. Lumican and keratan sulfate staining was similar or less intense in PE compared with the corneal stroma.
Identify location of PE and its immunohistochemical features.
In contrast to the widely accepted definition of PE as a prominent, anteriorly displaced Schwalbe line, histologic evidence suggests that it is a direct extension of the corneal stroma with variable locations that may displace the attenuated Descemet membrane when located anterior to or at Schwalbe's line. Immunohistochemical examination revealed that the composition of PE's extracellular matrix was similar to corneal stroma but with some variability in staining intensity.
本系列描述了后发性胚胎突(PE)的免疫病理学特征,并表明它不是通常描述的前移位的施万氏线,而是位置可变的周边角膜基质小结,其细胞外基质异常。
病例系列。
PE 患者的存档标本。
对存档的福尔马林固定、石蜡包埋标本(n=9;7 例尸检和 2 例小梁切除术标本)进行光镜检查。对 5 个标本进行免疫组织化学染色,以表征 PE 的细胞外基质组成。
PE 表现为从角膜基质延伸的漩涡状胶原小结,在某些情况下,由角膜内皮膜排列。这些小结位于施万氏线(n=4)之前、之后(n=1)、部分嵌入小梁网(n=1)或施万氏线(n=2)。定性地,PE 基质的 I 型胶原标记与角膜基质相似或较弱,而 III 型胶原染色则与角膜基质相比具有局灶性和稍强的强度。与角膜基质相比,亮氨酸和硫酸角质素染色在 PE 中相似或较弱。
确定 PE 的位置及其免疫组织化学特征。
与广泛接受的将 PE 定义为突出的、前移位的施万氏线相反,组织学证据表明,它是角膜基质的直接延伸,其位置可变,当位于施万氏线之前或施万氏线时,可能会使变弱的角膜内皮膜移位。免疫组织化学检查显示,PE 的细胞外基质组成与角膜基质相似,但染色强度存在一些可变性。