Kasetsuwan Ngamjit, Reinprayoon Usanee, Chantaren Patchima
Department of Ophthalmology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand ; Ophthalmology Department, King Chulalongkorn Memorial Hospital, Bangkok, Thailand.
Ophthalmology Department, King Chulalongkorn Memorial Hospital, Bangkok, Thailand.
Int Med Case Rep J. 2015 Sep 28;8:219-23. doi: 10.2147/IMCRJ.S83892. eCollection 2015.
To present a case of syphilitic interstitial keratitis with Descemet's scrolls, as well as its characteristic findings in an anterior segment investigation in relation to the histopathologic findings from a literature review.
A case report of a 64-year-old woman with syphilitic infection presented with band keratopathy and retrocorneal scrolls. Slit-lamp photography, confocal microscopy, anterior segment optical coherence tomography (AS-OCT), and ultrasound biomicroscopy were performed. Four previous reports were reviewed to describe the pathogenesis, natural history, and histopathologic and immunohistologic findings of the Descemet's scroll.
The spectacle-corrected visual acuity was 20/50 and 20/30 in the right and left eyes, respectively. The scrolls appeared as a translucent web extending from Descemet's membrane into the anterior chamber. Confocal microscopy showed decreased endothelial cell density, pleomorphism, polymegathism, and hyperreflective fibrocellular rods with central hollow. The AS-OCT and ultrasound biomicroscopy showed rod-shaped retrocorneal scrolls. The corneal thickness was 494 microns, as measured by AS-OCT. The corneal lesion remained stable during the 6-year follow-up period without the need for keratoplasty, while the previous literature reported spontaneous and postoperative corneal decompensation.
We present a case of syphilitic interstitial keratitis with rare Descemet's scrolls featuring relatively good visual acuity. Although we did not obtain the corneal tissue for examination, the anterior segment investigation provides insight into the underlying histopathology and natural disease history. The central hollow and cellular component seen during confocal microscopy might correspond to the amorphous core and the abnormal endothelial cells in the histopathologic findings. Failure to detect the corneal endothelium due to stromal opacity in these cases is possible, however, compromised endothelium may present.
报告一例伴有Descemet膜卷曲的梅毒性间质性角膜炎病例,并结合文献回顾中的组织病理学发现,阐述其在前节检查中的特征性表现。
一名64岁梅毒感染女性患者,表现为带状角膜病变和角膜后卷曲。进行了裂隙灯照相、共焦显微镜检查、前节光学相干断层扫描(AS-OCT)和超声生物显微镜检查。回顾了之前的4篇报告,以描述Descemet膜卷曲的发病机制、自然病程以及组织病理学和免疫组织化学发现。
右眼和左眼的矫正视力分别为20/50和20/30。卷曲表现为从Descemet膜延伸至前房的半透明网状物。共焦显微镜检查显示内皮细胞密度降低、细胞大小不一、形态各异以及中央中空的高反射纤维细胞棒。AS-OCT和超声生物显微镜检查显示角膜后有棒状卷曲。通过AS-OCT测量,角膜厚度为494微米。在6年的随访期内,角膜病变保持稳定,无需进行角膜移植术,而之前的文献报道有自发性和术后角膜失代偿情况。
我们报告了一例伴有罕见Descemet膜卷曲且视力相对较好的梅毒性间质性角膜炎病例。尽管我们未获取角膜组织进行检查,但前节检查为潜在的组织病理学和疾病自然史提供了见解。共焦显微镜检查中所见的中央中空和细胞成分可能与组织病理学发现中的无定形核心和异常内皮细胞相对应。然而,在这些病例中,由于基质混浊可能无法检测到角膜内皮,但内皮功能可能已受损。