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累及眼附属器的自然杀伤/T 细胞淋巴瘤的临床特征和治疗结果。

Clinical characteristics and treatment outcomes of natural killer/T-cell lymphoma involving the ocular adnexa.

机构信息

Department of Ophthalmology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.

Department of Ophthalmology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea

出版信息

Br J Ophthalmol. 2019 Feb;103(2):269-273. doi: 10.1136/bjophthalmol-2017-311704. Epub 2018 Apr 29.

Abstract

AIMS

To evaluate the clinical characteristics and treatment outcomes of natural killer/T-cell lymphoma (NKTL) involving the ocular adnexa.

METHODS

Retrospective, comparative, observational case series. A total of 350 patients with NKTL, including 27 patients with NKTL involving the ocular adnexa from 1999 to 2016. The patients were grouped into two groups: group 1 comprised patients presenting with ophthalmic symptoms, and group 2 comprised patients presenting with symptoms from other organs but subsequently developed ophthalmic involvement.

RESULTS

Group 1 comprised 12 patients (44.4%) and group 2 comprised 15 (55.6%). Mean duration of symptoms in group 1 was 1.8±1.2 months, while the time from diagnosis of NKTL to development of ophthalmic symptoms in group 2 was 45.3±65.6 months. Periorbital swelling was the most common presenting symptom in both groups (83.3% in group 1 and 73.3% in group 2). Symptoms mimicking cellulitis and pseudotumor were present in 50.0% and 16.7% of cases, respectively. The 5-year overall survival rate was 18.5% in group 1 and 26.4% in group 2, while the 5-year progression-free survival rate was 0% and 13.3%, respectively.

CONCLUSIONS

Our series is to our knowledge the largest cohort study on NKTL reported to date and demonstrates that ocular adnexal NKTL is a rare but seriously fatal disease. It is characterised by acute inflammatory signs as present in as many as two-thirds of our patients in this series. It should be considered as a differential diagnosis in patients presenting with rapidly progressing proptosis and diagnosed promptly for optimal management.

摘要

目的

评估涉及眼附属器的自然杀伤细胞/ T 细胞淋巴瘤(NKTL)的临床特征和治疗结果。

方法

回顾性、对比、观察性病例系列研究。共纳入 350 例 NKTL 患者,其中 27 例 NKTL 累及眼附属器,这些患者来自 1999 年至 2016 年。将患者分为两组:第 1 组包括以眼部症状就诊的患者,第 2 组包括以其他器官症状就诊但随后出现眼部受累的患者。

结果

第 1 组包括 12 例患者(44.4%),第 2 组包括 15 例患者(55.6%)。第 1 组的症状持续时间平均为 1.8±1.2 个月,而第 2 组从 NKTL 诊断到出现眼部症状的时间为 45.3±65.6 个月。眶周肿胀是两组中最常见的首发症状(第 1 组为 83.3%,第 2 组为 73.3%)。分别有 50.0%和 16.7%的病例出现类似蜂窝织炎和假性肿瘤的症状。第 1 组的 5 年总生存率为 18.5%,第 2 组为 26.4%,第 1 组的 5 年无进展生存率为 0%,第 2 组为 13.3%。

结论

本研究是迄今为止关于 NKTL 的最大队列研究,表明眼附属器 NKTL 是一种罕见但严重致命的疾病。其特征是急性炎症表现,在本研究的多达三分之二的患者中存在这种表现。在出现快速进展性眼球突出的患者中,应将其视为鉴别诊断,并及时诊断以获得最佳治疗效果。

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