沙特人群中的盘状红斑狼疮:临床和组织病理学研究

Fahad M. Al-Saif, Amal O. Al-Balbeesi, Abdullah I. Al-Samary, Saleh B. Al-Rashid, Mona Halwani, Eman Al-Mekhadab, Mona Al-Kelabi
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引用次数: 6

摘要

我们报道了一组沙特阿拉伯患者的盘状红斑狼疮(DLE)的临床和组织病理学特征,并为随后更大规模的前瞻性研究提供了基本框架。方法回顾性分析1998年1月至2010年12月在沙特阿拉伯利雅得的沙特国王大学哈立德国王大学医院皮肤科门诊就诊和诊断的dle患者。数据包括人口统计学、病程、诱发和加重因素、临床类型、免疫标志物和组织病理学结果。结果56例DLE患者中,女性比男性多1.5:1。平均发病年龄36.5±13.7岁,平均病程18.5±24.6个月。萎缩型占绝大多数(91.1%)。头皮和面部是最常见的受累部位。抗核抗体(ANA)阳性9例(16.1%)。8例(14.3%)DsDNA阳性。52例(92.9%)表现为真皮浸润,38例(67.9%)表现为阑尾周围浸润,31例(55.4%)表现为地衣样反应和空泡变性。51例(91.1%)患者接受治疗;31例(60.8%)病变改善,6例(11.8%)进展为系统性红斑狼疮(SLE)。疾病的进展与发病年龄显著相关(p = 0.044),但与病程、性别、免疫标志物、组织病理学特征或治疗无关。结论部分患者发展为系统性狼疮的倾向性应引起重视,早期诊断、患者教育和适当的管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Discoid lupus erythematosus in a Saudi population: Clinical and histopathological study

Background

We report the clinical and histopathological features of discoid lupus erythematosus (DLE) in a group of Saudi patients, and provide a basic framework for a subsequent larger, prospective study.

Methods

DLE patients seen and diagnosed at the Dermatology Clinic of King Khalid University Hospital, King Saud University, Riyadh, Saudi Arabia, between January 1998 and December 2010 were retrospectively studied. Data included demographics, duration of the disease, precipitating and aggravating factors, clinical type, immunological markers and histopathological findings.

Results

Of the 56 DLE patients, females outnumbered males by 1.5:1. Mean age of onset was 36.5 ± 13.7 years and mean duration of the disease was 18.5 ± 24.6 months. Majority of patients (91.1%) had atrophic type. The scalp and face were the commonest sites of involvement. Antinuclear antibodies (ANA) were positive in nine patients (16.1%). Eight (14.3%) were positive for DsDNA. Fifty-two (92.9%) showed dermal infiltration, 38 (67.9%) with periappendigeal infiltrates and 31 (55.4%) with lichenoid reaction and vacuolar degeneration. Fifty-one patients (91.1%) received treatment; 31 (60.8%) had improvement of the lesions whereas six patients (11.8%) progressed to systemic lupus erythematosus (SLE). Progression of the disease was significantly correlated with age of onset (p = 0.044) but not to duration of the disease, gender, immunological markers, histopathological features or treatment.

Conclusion

The propensity of some patients progressing to systemic lupus should be given attention through early diagnosis, patient education and appropriate management.

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