眼眶反应性淋巴样增生:病例系列及文献回顾。

IF 1.4 4区 医学 Q3 OPHTHALMOLOGY
Ayodeji Ajanaku, Matthew Fenech, Nima Ghadiri, Sarah E Coupland
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引用次数: 0

摘要

本研究旨在描述一个病例系列的患者诊断为眼眶反应性淋巴样增生(RLH)在单一三级保健中心。通过搜索利物浦大学NHS基金会信托基金(LUHFT)从2021年12月1日至2023年12月1日的电子病历进行回顾性审查,以确定所有组织学诊断的患者。10例患者的眼眶组织学诊断为RLH。诊断时的中位年龄为56.5岁。突出是最常见的症状,其他体征包括可触及的肿块、上睑下垂和复视。8例患者接受口服强的松龙治疗,20%(2例)患者获得完全缓解。在这些病例中使用的其他治疗包括强力霉素、霉酚酸盐、环孢素和硫唑嘌呤。本病例系列是为数不多的专注于轨道RLH的报告之一。值得注意的是,在这项研究中观察到骨质侵蚀,这一发现在文献中几乎没有与RLH联系起来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Orbital reactive lymphoid hyperplasia: Case series and literature review.

This study aimed to describe a case series of patients diagnosed with orbital reactive lymphoid hyperplasia (RLH) at a single tertiary care centre. A retrospective review was conducted by searching electronic medical records at Liverpool University NHS Foundation Trust (LUHFT) from 1st December 2021 - 1st December 2023, to identify all patients with a histological diagnosis. Ten patients with an orbital histological diagnosis of RLH were identified. Median age at diagnosis was 56.5 years. Proptosis was the most prevalent presenting symptom, while other signs included palpable mass, ptosis, and diplopia. Eight patients were treated with oral prednisolone, with 20% (two) achieving complete remission. Additional treatments utilised in these cases encompassed doxycycline, mycophenolate, ciclosporin, and azathioprine.This case series represents one of the few reports focusing exclusively on orbital RLH. Notably, bone erosion was observed in this study, a finding that has been scarcely linked to RLH in the literature.

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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
372
审稿时长
3-8 weeks
期刊介绍: The European Journal of Ophthalmology was founded in 1991 and is issued in print bi-monthly. It publishes only peer-reviewed original research reporting clinical observations and laboratory investigations with clinical relevance focusing on new diagnostic and surgical techniques, instrument and therapy updates, results of clinical trials and research findings.
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