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系统性红斑狼疮的特征。在一家综合医院开展的一项研究。

The characteristics of systemic lupus erythematosus. A study in a general hospital.

作者信息

Karadsheh M F, Nimri F A, Ajlouni Y M, Dneibat W A, Karadsheh R F

机构信息

Department of Medicine, King Hussein Medical Centre, PO Box 1031, Madaba 17110, Jordan.

出版信息

Saudi Med J. 2000 Mar;21(3):282-6.

Abstract

OBJECTIVE

There is a wide variation in the natural history of Systemic Lupus Erythematosus among different ethnic and geographical groups. Studies in Arabs are few. This study aims to demonstrate the clinical characteristics of Systemic Lupus Erythematosus patients in Jordanians.

METHODS

A retrospective review of the records of the cases diagnosed as Systemic Lupus Erythematosus in a tertiary referral centre (King Hussein Medical Centre) over the years 1991-1997. The records were analyzed for age, sex, presentation, diagnostic criteria, investigations, complications and treatment.

RESULTS

Seventy-six records were analyzed. The patients were from all parts of Jordan, with a mean age of 20 years. The female: male ratio was 24:1. The presentation was arthralgia-arthritis in 68 (89%) patients; skin manifestations in the form of malar rash in 32 (42%), photosensitivity in 19 (25%). Central nervous system manifestations were also noted in 21 (27%) of the patients. Anti-nuclear antibodies were positive in 71 (93%) patients, anti double stranded DNA (DsDNA) positive in 80%. Anemia and leukopenia or both were noted in 52 patients(69%). Erythrocyte Sedimentation Rate was more than 30mm in the first hour in 49 (88%) patients. Lupus anticoagulants were negative in 75% of patients, renal impairment was documented in 46% of the patients (35 patients) with positive correlation to DsDNA. All the patients received steroids, 95% (73) in the form of prednisolone and 5% in the form of methylprednisolone; cytotoxics either cyclophosphamide or azathioprine mainly for renal disease were prescribed to 25 patients, Complications were hypertension (18 patients), renal failure (7 patients), cerebral vascular disease (3 patients). Death was recorded in 3 subjects within 1-4 years of diagnosis

CONCLUSION

This study demonstrates the presentations of Systemic Lupus Erythematosus patients with a high incidence of complications, which may be due to late presentation or late diagnosis. Further studies are needed on the natural history of this disease in Jordanians.

摘要

目的

系统性红斑狼疮在不同种族和地理区域人群中的自然病史差异很大。针对阿拉伯人的相关研究较少。本研究旨在阐明约旦系统性红斑狼疮患者的临床特征。

方法

对1991年至1997年期间在一家三级转诊中心(侯赛因国王医疗中心)确诊为系统性红斑狼疮的病例记录进行回顾性分析。分析记录中的年龄、性别、临床表现、诊断标准、检查、并发症及治疗情况。

结果

共分析了76份记录。患者来自约旦各地,平均年龄20岁。男女比例为24∶1。68例(89%)患者表现为关节痛-关节炎;32例(42%)患者有以颊部皮疹形式出现的皮肤表现,19例(25%)有光敏现象。21例(27%)患者还出现中枢神经系统表现。71例(93%)患者抗核抗体呈阳性,80%患者抗双链DNA(DsDNA)呈阳性。52例患者(69%)出现贫血和白细胞减少或两者皆有。49例(88%)患者第一小时红细胞沉降率超过30mm。75%患者狼疮抗凝物呈阴性,46%患者(35例)有肾功能损害,且与DsDNA呈正相关。所有患者均接受了类固醇治疗,95%(73例)为泼尼松龙,5%为甲泼尼龙;25例患者因肾病主要接受了环磷酰胺或硫唑嘌呤等细胞毒性药物治疗。并发症包括高血压(18例)、肾衰竭(7例)、脑血管疾病(3例)。3例患者在确诊后1至4年内死亡。

结论

本研究展示了系统性红斑狼疮患者的临床表现及高并发症发生率,这可能归因于就诊延迟或诊断延迟。需要对约旦人群中该病的自然病史做进一步研究。

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