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美国南部的巨细胞动脉炎。一项来自得克萨斯湾沿岸的11年回顾性研究。

Giant-cell arteritis in the southern United States. An 11-year retrospective study from the Texas Gulf Coast.

作者信息

Gonzalez E B, Varner W T, Lisse J R, Daniels J C, Hokanson J A

机构信息

Department of Internal Medicine, University of Texas Medical Branch, Galveston.

出版信息

Arch Intern Med. 1989 Jul;149(7):1561-5.

PMID:2742429
Abstract

Giant-cell arteritis (GCA) and polymyalgia rheumatica are systemic disorders that reportedly affect primarily white women older than age 50 years. We conducted an 11-year chart review to determine the relative occurrence and pattern of demographic involvement of GCA in the Gulf Coast region of the United States. Of 101,239 computer-coded entries for individual patients aged 40 years or older, 60 charts listed GCA as a differential diagnosis. Twenty-seven patients had temporal GCA; 21 temporal artery biopsy specimens were identified. Two patients had associated systemic GCA (one with aortitis). A striking finding was that 13 of the 27 patients were black women (about 50% of the entire study population). The group with GCA and polymyalgia rheumatica (17 patients) had a significantly higher mean erythrocyte sedimentation rate than the group with "pure" GCA. Jaw claudication and blindness were rare. We concluded that temporal GCA seems relatively uncommon in the Gulf Coast region and in the southern United States as a whole. Furthermore, GCA seems rare in Hispanics (only one patient identified). Nonetheless, this is the first report to document a proportionally high occurrence of GCA in black patients in this part of the country.

摘要

巨细胞动脉炎(GCA)和风湿性多肌痛是据报道主要影响50岁以上白人女性的全身性疾病。我们进行了一项为期11年的病历回顾,以确定美国墨西哥湾沿岸地区GCA的相对发病率及人口统计学参与模式。在101239份40岁及以上个体患者的计算机编码记录中,60份病历将GCA列为鉴别诊断。27例患者患有颞动脉GCA;确定了21份颞动脉活检标本。2例患者伴有全身性GCA(1例伴有主动脉炎)。一个显著发现是,27例患者中有13例为黑人女性(约占整个研究人群的50%)。患有GCA和风湿性多肌痛的组(17例患者)的平均红细胞沉降率显著高于“单纯”GCA组。颌部间歇性运动障碍和失明较为罕见。我们得出结论,颞动脉GCA在墨西哥湾沿岸地区以及整个美国南部似乎相对不常见。此外,GCA在西班牙裔中似乎罕见(仅识别出1例患者)。尽管如此,这是该国该地区首份记录黑人患者中GCA比例较高发生率的报告。

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