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采用深板层角膜移植术治疗黏多糖贮积症I型相关角膜病变的多模态成像

Multimodal imaging of Hurler syndrome-related keratopathy treated with deep anterior lamellar keratoplasty.

作者信息

Da Cunha Elodie, Georgeon Cristina, Bouheraoua Nacim, Putterman Marc, Brignole-Baudouin Françoise, Borderie Vincent M

机构信息

GRC32, Transplantation et Thérapies Innovantes de la Cornée, Sorbonne université, Centre Hospitalier National d'Ophtalmologie des 15-20, 28 rue de Charenton, 75571 Cedex 12, Paris, France.

Laboratoire (2), Centre Hospitalier National d'Ophtalmologie des 15-20, Paris, France.

出版信息

BMC Ophthalmol. 2020 Oct 31;20(1):433. doi: 10.1186/s12886-020-01689-2.

Abstract

BACKGROUND

Hurler syndrome-associated keratopathy is an exceedingly rare corneal disorder that requires corneal transplantation in advanced stages. Precise assessment of the corneal condition is necessary for deciding which type of keratoplasty (i.e., deep anterior lamellar or penetrating) should be proposed. We aimed to confront the results of multimodal imaging with those of histology in a case of Hurler syndrome-associated keratopathy.

CASE PRESENTATION

A 16-year-old patient with Hurler's syndrome treated with hematopoietic stem cell transplantation was referred for decreased vision related to advanced keratopathy. The patient was treated with deep anterior lamellar keratoplasty (DALK) in both eyes with uncomplicated outcome. Visual acuity improved from 0.1 (20/200) preoperatively to 0.32 (20/63) and 0.63 (20/32) after transplantation. The corneal endothelial cell density was 2400 cells/mm in both eyes 3 years after transplantation. In vivo confocal microscopy (IVCM) and spectral domain optical coherence tomography (SD-OCT) were performed preoperatively. The corneal buttons retrieved during keratoplasty were processed for histology. In SD-OCT scans, corneal opacities appeared as diffuse stromal hyperreflectivity associated with increased corneal thickness. IVCM showed diffuse cytoplasmic granular hyperreflectivity and rounded/ellipsoid aspects of keratocytes, presence of small intracellular vacuoles, and hyperreflective epithelial intercellular spaces. Bowman's layer was thin and irregular. The corneal endothelium was poorly visualized but no endothelial damage was observed. Histology showed irregular orientation and organization of stromal lamellae, with the presence of macrophages whose cytoplasm appeared clear and granular. A perinuclear clear halo was visible within the epithelial basal cells. Bowman's layer featured breaks and irregularities.

CONCLUSIONS

The observed corneal multimodal imaging features in mucopolysaccharidosis-related keratopathy were concordant with histology. Compared with standard histology, multimodal imaging allowed additional keratocyte features to be observed. It revealed both morphological and structural changes of all corneal layers but the endothelium. This information is essential for therapeutic management which should include DALK as the first-choice treatment in case of impaired visual acuity.

摘要

背景

黏多糖贮积症I型(Hurler综合征)相关角膜病变是一种极为罕见的角膜疾病,晚期需要进行角膜移植。准确评估角膜状况对于决定应采用哪种角膜移植术(即深板层角膜移植术或穿透性角膜移植术)至关重要。我们旨在对比黏多糖贮积症I型相关角膜病变病例的多模态成像结果与组织学结果。

病例报告

一名接受造血干细胞移植治疗的16岁黏多糖贮积症I型患者因晚期角膜病变导致视力下降前来就诊。该患者双眼接受了深板层角膜移植术(DALK),术后恢复顺利。视力从术前的0.1(20/200)提高到移植后的0.32(20/63)和0.63(20/32)。移植3年后,双眼角膜内皮细胞密度为2400个细胞/mm²。术前进行了共聚焦显微镜检查(IVCM)和频域光学相干断层扫描(SD-OCT)。角膜移植术中取下的角膜植片进行了组织学处理。在SD-OCT扫描中,角膜混浊表现为弥漫性基质高反射,伴有角膜厚度增加。IVCM显示角膜细胞弥漫性细胞质颗粒高反射及圆形/椭圆形外观,存在小的细胞内空泡,上皮细胞间隙高反射。Bowman层薄且不规则。角膜内皮难以清晰显示,但未观察到内皮损伤。组织学显示基质板层排列和组织不规则,存在巨噬细胞,其细胞质呈透明颗粒状。上皮基底细胞内可见核周透明晕。Bowman层有断裂和不规则。

结论

在黏多糖贮积症相关角膜病变中观察到的角膜多模态成像特征与组织学结果一致。与标准组织学相比,多模态成像能够观察到额外的角膜细胞特征。它揭示了除内皮外所有角膜层的形态和结构变化。这些信息对于治疗管理至关重要,在视力受损的情况下,治疗应首选DALK。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe15/7603712/42d2828c38ea/12886_2020_1689_Fig1_HTML.jpg

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