Academic Unit of Ophthalmology, University of Birmingham, Birmingham, UK.
Department of Ophthalmology, Birmingham and Midland Eye Centre, Birmingham, UK.
Br J Ophthalmol. 2018 Oct;102(10):1362-1366. doi: 10.1136/bjophthalmol-2017-311612. Epub 2018 Jan 6.
The diagnosis of primary vitreoretinal lymphoma (PVRL) poses significant difficulties; presenting features are non-specific and confirmation usually necessitates invasive vitreoretinal biopsy. Diagnosis is often delayed, resulting in increased morbidity and mortality. Non-invasive imaging modalities such as spectral domain optical coherence tomography (SD-OCT) offer simple and rapid aids to diagnosis. We present characteristic SD-OCT images of patients with biopsy-positive PVRL and propose a number of typical features, which we believe are useful in identifying these lesions at an early stage.
Medical records of all patients attending Moorfields Eye Hospital between April 2010 and April 2016 with biopsy-positive PVRL were reviewed. Pretreatment SD-OCT images were collected for all eyes and were reviewed independently by two researchers for features suggestive of PVRL.
Pretreatment SD-OCT images of 32 eyes of 22 patients with biopsy-proven PVRL were reviewed. Observed features included hyper-reflective subretinal infiltrates (17/32), hyper-reflective infiltration in inner retinal layers (6/32), retinal pigment epithelium (RPE) undulation (5/32), clumps of vitreous cells (5/32) and sub-RPE deposits (3/32). Of these, the hyper-reflective subretinal infiltrates have an appearance unique to PVRL, with features not seen in other diseases.
We have identified a range of SD-OCT features, which we believe to be consistent with a diagnosis of PVRL. We propose that the observation of hyper-reflective subretinal infiltrates as described is highly suggestive of PVRL. This case series further demonstrates the utility of SD-OCT as a non-invasive and rapid aid to diagnosis, which may improve both visual outcomes and survival of patients with intraocular malignancies such as PVRL.
原发性玻璃体视网膜淋巴瘤(PVRL)的诊断存在较大困难;其临床表现不具特异性,确诊通常需要进行有创性玻璃体视网膜活检。由于诊断常常被延误,患者的发病率和死亡率均有所增加。光谱域光学相干断层扫描(SD-OCT)等非侵入性成像方式为诊断提供了简便、快捷的辅助手段。我们展示了经活检证实的 PVRL 患者的典型 SD-OCT 图像,并提出了一些典型特征,我们认为这些特征有助于早期识别这些病变。
回顾 2010 年 4 月至 2016 年 4 月期间在 Moorfields 眼科医院就诊并经活检证实为 PVRL 的所有患者的病历。收集所有患者的治疗前 SD-OCT 图像,并由两名研究人员独立评估提示 PVRL 的特征。
共评估了 22 例 32 只眼经活检证实的 PVRL 患者的治疗前 SD-OCT 图像。观察到的特征包括:视网膜下高反射性浸润(17/32)、内视网膜层高反射性浸润(6/32)、视网膜色素上皮(RPE)波动(5/32)、玻璃体细胞团块(5/32)和视网膜下沉积物(3/32)。其中,视网膜下高反射性浸润具有 PVRL 特有的表现,与其他疾病不同。
我们已经确定了一系列 SD-OCT 特征,我们认为这些特征与 PVRL 的诊断相符。我们提出,如所述观察到视网膜下高反射性浸润高度提示 PVRL。本病例系列进一步证明了 SD-OCT 作为一种非侵入性、快速的诊断辅助手段的实用性,这可能改善 PVRL 等眼内恶性肿瘤患者的视力预后和生存。