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马来西亚一家风湿病中心系统性硬化症的人口统计学、临床及实验室特征

Demography, clinical and laboratory features of systemic sclerosis in a Malaysian rheumatology centre.

作者信息

Pagalavan L, Ong S G

机构信息

Rheumatology Unit, Department of Medicine, Hospital Selayang, 68100 Batu Caves, Selangor.

出版信息

Med J Malaysia. 2007 Jun;62(2):117-21.

Abstract

A six year retrospective study of the demography, clinical and laboratory features of patients with systemic sclerosis (SSc) was carried out in Selayang Hospital. There were 61 cases seen between January 2000 and December 2005. Of these, 55 (90.2%) were females and 6 (9.8%) were males. Twenty-eight (45.9%) were Malays, 24 (39.3%) were Chinese and 9 (14.8%) were Indians. The mean age of onset was 38.8 years. Thirty-nine (64.0%) had limited cutaneous SSc, 21 (34.4%) had diffuse cutaneous SSc and one had localized morphoea. Raynaud's phenomenon was present in 82.6%, telangiectasia in 45.9%, calcinosis in 11.5%, sclerodactyly in 83.6%, digital pitting scars in 42.6%, digital infarcts/ulcers/gangrene in 23.0%, arthralgia/arthritis in 49.2% and gastroesophageal reflux disease (GERD) in 47.5%. Forty-three (70.5%) patients had interstitial lung disease. Seven patients had associated myositis, 7 systemic lupus erythematosus and 2 rheumatoid arthritis. Three had two other connective tissue diseases. Antinuclear antibodies were positive in 83.6% and anti-Scl 70 antibodies in 34.4%. This study demonstrates that limited cutaneous SSc is more common and there is a high incidence of interstitial lung disease in our population.

摘要

在斯里央医院对系统性硬化症(SSc)患者的人口统计学、临床和实验室特征进行了一项为期六年的回顾性研究。2000年1月至2005年12月期间共诊治61例患者。其中,女性55例(90.2%),男性6例(9.8%)。马来人28例(45.9%),华人24例(39.3%),印度人9例(14.8%)。平均发病年龄为38.8岁。局限性皮肤型SSc患者39例(64.0%),弥漫性皮肤型SSc患者21例(34.4%),局限性硬斑病患者1例。雷诺现象发生率为82.6%,毛细血管扩张为45.9%,钙质沉着为11.5%,指端硬化为83.6%,指腹点状瘢痕为42.6%,指端梗死/溃疡/坏疽为23.0%,关节痛/关节炎为49.2%,胃食管反流病(GERD)为47.5%。43例(70.5%)患者患有间质性肺病。7例患者合并肌炎,7例合并系统性红斑狼疮,2例合并类风湿关节炎。3例患者合并另外两种结缔组织病。抗核抗体阳性率为83.6%,抗Scl 70抗体阳性率为34.4%。本研究表明,局限性皮肤型SSc在我国更为常见,且间质性肺病发病率较高。

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