Spitz Meredith P, Anderson David R, Vrabec Tamara R
Geisinger Eye Institute, Danville, PA, USA.
Retina Consultants of Minnesota, Edina, MN, USA.
Am J Ophthalmol Case Rep. 2024 Sep 7;36:102166. doi: 10.1016/j.ajoc.2024.102166. eCollection 2024 Dec.
To describe the clinical, laboratory and multimodal imaging findings in paraneoplastic autoimmune retinopathy (p-AIR) associated with anti-pyruvate kinase M2 antibody (anti-PKM2) and occult pancreatic adenocarcinoma.
A 70 year old male with blurred vision, nyctalopia and concurrent difficulty with glucose control had retinal vascular attenuation and diffuse punctate pigment clumping in both eyes. Multimodal imaging demonstrated corresponding stippled hypofluorescence on fluorescein angiography, stippled hyperautofluorescence and a hyperautoflourescent macular ring with fundus autofluorescence, and focal hyperreflectivity at the level of the RPE-Bruch's membrane complex with diffuse loss of outer retinal layers on ocular coherence tomography. In addition, diffuse ganglion cell loss and severe visual field constriction were present. Genetic testing for retinitis pigmentosa was normal. Screening for anti-retinal antibodies was positive for only anti-PKM2. Systemic evaluation revealed previously undiagnosed adenocarcinoma of the pancreas.
Anti-PKM2 in the setting of autoimmune retinopathy may be associated with occult pancreatic cancer. The diagnosis of pAIR should be considered and systemic investigation for occult malignancy initiated even in the absence of more commonly associated anti-retinal antibodies.
描述与抗丙酮酸激酶M2抗体(抗PKM2)及隐匿性胰腺腺癌相关的副肿瘤性自身免疫性视网膜病变(p-AIR)的临床、实验室及多模态影像学表现。
一名70岁男性,有视力模糊、夜盲症且同时存在血糖控制困难,双眼出现视网膜血管变细及散在点状色素沉着。多模态影像学检查显示,荧光素血管造影有相应的点状低荧光,眼底自发荧光有散在点状高自发荧光及一个高自发荧光的黄斑环,光学相干断层扫描显示视网膜色素上皮- Bruch膜复合体层面有局灶性高反射,同时外层视网膜弥漫性缺失。此外,存在弥漫性神经节细胞丢失及严重的视野缩窄。视网膜色素变性的基因检测结果正常。仅抗PKM2的抗视网膜抗体筛查呈阳性。全身评估发现此前未被诊断出的胰腺腺癌。
自身免疫性视网膜病变情况下的抗PKM2可能与隐匿性胰腺癌有关。即使没有更常见的相关抗视网膜抗体,也应考虑pAIR的诊断并启动对隐匿性恶性肿瘤的全身检查。