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眼内结外自然杀伤/T 细胞淋巴瘤继发于腹膜后肿瘤的首次观察:病例报告和对比分析。

First observation of intraocular extranodal natural killer/T-cell lymphoma secondary to a retroperitoneal tumour: a case report and comparative review.

机构信息

State Key Laboratory of Ophthalmology, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Zhongshan Ophthalmic Center, Sun Yat-Sen University, Guangzhou, 510060, China.

Guangdong Provincial Clinical Research Center for Ocular Diseases, Guangzhou, China.

出版信息

BMC Ophthalmol. 2022 Mar 26;22(1):141. doi: 10.1186/s12886-022-02362-6.

Abstract

BACKGROUND

Vitreoretinal lymphomas are difficult to diagnose due to their insidious onset and inaccessible focal points. Natural killer/T-cell derived malignancies are rare as intraocular lymphomas and usually have a rapid progression and a poor prognosis. Therefore, it is essential to make a definite diagnosis, especially differentially with B-cell-derived lymphomas, which account for most cases of vitreoretinal lymphomas.

CASE PRESENTATION

This case report describes a 55-year-old female reporting a 10-month history of painless decline in her vision of the right eye. Optical coherence tomography of the patient revealed hyperreflective nodules and irregular humps in the retinal pigment epithelium layer. The right vitreous was aspirated for diagnostic assessment, revealing an interleukin-10 level of 39.4 pg/mL and an interleukin-10/interleukin-6 ratio of 1.05. The right vitreous humor was positive for Epstein-Barr virus DNA. Upon a systemic examination, a high metabolic nodule was found in the retroperitoneal area and proven to be positive for Epstein-Barr virus-encoded mRNA, CD2, CD3ε, TIA-1, and Ki-67. Considering the homology of the two lesions, the patient was diagnosed with metastatic vitreoretinal lymphoma secondary to retroperitoneal extranodal natural killer/T-cell derived lymphoma. The patient received systemic chemotherapy and regular intravitreal injections of methotrexate. Her visual acuity of the right eye had improved from 20/125 to 20/32 at the latest follow-up. No new lesions were found.

CONCLUSIONS

A definitive diagnosis of vitreoretinal lymphoma is challenging. On some occasions in which pathological evidence is missing, the available examination results and clinical observations must be comprehensively considered. This study herein summarized pertinent pieces of literature and reports and reviewed available practicable methods to make a definitive diagnosis of intraocular extranodal natural killer/T-cell lymphoma, which was particularly distinct from the common diffuse large B-cell lymphomas.

摘要

背景

由于玻璃体视网膜淋巴瘤的隐匿性发病和难以触及的焦点,其诊断较为困难。自然杀伤/ T 细胞衍生的恶性肿瘤作为眼内淋巴瘤较为罕见,通常进展迅速,预后较差。因此,明确诊断至关重要,尤其是与占大多数玻璃体视网膜淋巴瘤的 B 细胞衍生淋巴瘤进行鉴别诊断。

病例介绍

本病例报告描述了一名 55 岁女性,她自述右眼无痛性视力下降已有 10 个月。患者的光学相干断层扫描显示视网膜色素上皮层有高反射性小结节和不规则隆起。右眼玻璃体抽吸用于诊断评估,结果显示白细胞介素 10 水平为 39.4pg/ml,白细胞介素 10/白细胞介素 6 比值为 1.05。右眼玻璃体液 EBV-DNA 阳性。全身检查时,发现腹膜后区域有一个高代谢性结节,该结节 EBV 编码的 mRNA、CD2、CD3ε、TIA-1 和 Ki-67 均为阳性。鉴于两个病变的同源性,患者被诊断为腹膜后结外自然杀伤/T 细胞衍生淋巴瘤继发的转移性玻璃体视网膜淋巴瘤。患者接受了全身化疗和定期玻璃体内注射甲氨蝶呤。她右眼的视力从最初的 20/125 提高到了最后一次随访时的 20/32。未发现新的病变。

结论

玻璃体视网膜淋巴瘤的明确诊断具有挑战性。在某些情况下缺乏病理证据时,必须综合考虑现有检查结果和临床观察。本研究总结了相关文献和病例报告,并回顾了可行的诊断方法,以明确诊断眼内结外自然杀伤/T 细胞淋巴瘤,这与常见的弥漫性大 B 细胞淋巴瘤有明显不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3364/8962092/352f7b9ffe4d/12886_2022_2362_Fig1_HTML.jpg

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