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风湿性多肌痛和颞动脉炎:老年患者的管理

Polymyalgia rheumatica and temporal arteritis: managing older patients.

作者信息

Pereira M, Kaine J L

出版信息

Geriatrics. 1986 Jun;41(6):54-5, 59-60, 63 passim.

PMID:3710167
Abstract

PMR and GCA are diagnosed relatively frequently in the white geriatric population. Patients may suffer from both conditions or from either alone. PMR is considered a diagnosis of exclusion, with the most characteristic symptoms being profound morning stiffness affecting the hip and shoulder girdles. The diagnosis of PMR can be buttressed by the findings of an elevated ESR, anemia, and mildly elevated liver enzymes. PMR can be controlled with less than or equal to 20 mg/d of prednisone, whereas higher doses of glucocorticoids are required for GCA. Classic GCA is characterized by headache, visual changes, and constitutional symptoms. GCA can be confirmed by a biopsy revealing a histologic picture of granulomatous inflammation centered around the elastin of the involved vessel. Judicious efforts to taper steroids are indicated in both syndromes, but many patients require therapy for at least 2 years.

摘要

在老年白人人群中,巨细胞动脉炎(GCA)和风湿性多肌痛(PMR)的诊断相对常见。患者可能同时患有这两种疾病,也可能仅患其中一种。PMR被认为是一种排除性诊断,其最典型的症状是累及臀部和肩胛带的严重晨僵。红细胞沉降率(ESR)升高、贫血和肝酶轻度升高有助于PMR的诊断。PMR使用泼尼松剂量小于或等于20mg/d即可控制,而GCA则需要更高剂量的糖皮质激素。典型的GCA以头痛、视力改变和全身症状为特征。GCA可通过活检确诊,活检显示以受累血管弹性蛋白为中心的肉芽肿性炎症组织学表现。两种综合征均需谨慎减停类固醇,但许多患者至少需要治疗2年。

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