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华氏巨球蛋白血症视网膜病变的光学相干断层扫描血管造影特征:一例报告。

Optical coherence tomography angiography characteristics in Waldenström macroglobulinemia retinopathy: A case report.

作者信息

Li Jun, Zhang Rui, Gu Feng, Liu Zhe-Li, Sun Peng

机构信息

Department of Ophthalmology, The First Hospital of China Medical University, Shenyang 110001, Liaoning Province, China.

Department of Hematology, The First Hospital of China Medical University, Shenyang 110001, Liaoning Province, China.

出版信息

World J Clin Cases. 2020 Dec 6;8(23):6071-6079. doi: 10.12998/wjcc.v8.i23.6071.

Abstract

BACKGROUND

Waldenström macroglobulinemia (WM) is a distinct clinicopathologic entity characterized by the infiltration of the bone marrow by clonal lymphoplasmacytic cells that produce monoclonal immunoglobulin M (IgM) in the blood, and patients may present with symptoms related to the infiltration of the hematopoietic tissues or the effects of monoclonal IgM in the blood. Funduscopic abnormalities were noted in some of the patients due to hyperviscosity or other retinal lesions. Optical coherence tomography angiography (OCTA) as a non-invasive imaging tool can give qualitative and quantitative information about the status of retinal and choroidal vessels, which might be useful for diagnosing patients with WM-associated retinopathy.

CASE SUMMARY

The patient was a 67-year-old man who presented with sudden visual disturbance in both eyes. Ophthalmic tests showed that best corrected visual acuity (BCVA) for this patient was 20/100 in the right eye and 20/1000 in the left eye. Fundus examination, optical coherence tomography (OCT), and OCTA revealed substantial bilateral optic disc edema, dilated and tortuous retinal veins, and diffuse intraretinal blot hemorrhages and edema which were consistent with bilateral central retinal vein occlusion (CRVO). Meanwhile, remarkable bilateral serous macular detachments (SMD) were noticed on OCT. Systemic examinations showed that the patient had anemia and extremely high level of monoclonal IgM and infiltration of clonal lymphoplasmacytic cells in bone marrow. The diagnosis of WM with hyperviscosity and retinopathy was made based on the clinical manifestation and laboratory findings. He was subsequently treated with intravitreal ranibizumab injection, plasmapheresis, and bortezomib plus rituximab with dexamethasone. Six months after treatments, the central macular volume decreased by 16.1% in the right eye and 28.6% in the left eye on OCT, and the patient's BCVA was improved to 20/60 in the right eye and 20/400 in the left eye. Very good partial response was obtained after systemic treatment.

CONCLUSION

WM may affect visual function and present as bilateral CRVO. OCTA can show characteristic changes in both retina and choroid vasculatures, which might be of great value for diagnosing or following patients with WM retinopathy. Intravitreal anti-vascular endothelial growth factor treatment combined with systemic therapy might be beneficial for WM patients with retinopathy (SMD and CRVO).

摘要

背景

华氏巨球蛋白血症(WM)是一种独特的临床病理实体,其特征为骨髓被克隆性淋巴浆细胞浸润,这些细胞在血液中产生单克隆免疫球蛋白M(IgM),患者可能出现与造血组织浸润或血液中单体IgM作用相关的症状。部分患者因血液黏稠度增高或其他视网膜病变出现眼底异常。光学相干断层扫描血管造影(OCTA)作为一种非侵入性成像工具,可提供有关视网膜和脉络膜血管状态的定性和定量信息,这可能有助于诊断WM相关性视网膜病变患者。

病例摘要

该患者为一名67岁男性,双眼突发视力障碍。眼科检查显示,该患者右眼最佳矫正视力(BCVA)为20/100,左眼为20/1000。眼底检查、光学相干断层扫描(OCT)和OCTA显示双侧视神经盘明显水肿、视网膜静脉扩张迂曲、视网膜内弥漫性片状出血和水肿,符合双侧视网膜中央静脉阻塞(CRVO)。同时,OCT检查发现双侧显著的浆液性黄斑脱离(SMD)。全身检查显示患者有贫血、单克隆IgM水平极高以及骨髓中克隆性淋巴浆细胞浸润。根据临床表现和实验室检查结果,诊断为WM伴血液黏稠度增高和视网膜病变。随后,他接受了玻璃体内注射雷珠单抗、血浆置换以及硼替佐米联合利妥昔单抗加地塞米松治疗。治疗6个月后,OCT检查显示右眼黄斑中心凹体积减少16.1%,左眼减少28.6%,患者的BCVA右眼提高到20/60,左眼提高到20/400。全身治疗后获得了非常好的部分缓解。

结论

WM可能影响视觉功能并表现为双侧CRVO。OCTA可显示视网膜和脉络膜血管系统的特征性变化,这对于诊断或随访WM视网膜病变患者可能具有重要价值。玻璃体内抗血管内皮生长因子治疗联合全身治疗可能对患有视网膜病变(SMD和CRVO)的WM患者有益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0caa/7723702/01830163a09a/WJCC-8-6071-g001.jpg

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