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混合性结缔组织病的关节炎

The arthritis of mixed connective tissue disease.

作者信息

Bennett R M, O'Connell D J

出版信息

Ann Rheum Dis. 1978 Oct;37(5):397-403. doi: 10.1136/ard.37.5.397.

Abstract

Twenty patients with mixed connective tissue disease were followed for 5 years. Arthritis occurred in all 20 patients, being the presenting complaint in 11 patients. The joints most frequently involved were the proximal interphalangeal (PIP), metacarpophalangeal (MCP), wrists, metatarsophalangeal (MTP), and knee; the distribution tended to be symmetrical, mimicking early rheumatoid arthritis. Joint deformities occurred in 6 patients, but apart from 1 patient with arthritis mutilans, significant functional impairment was not encountered. Radiologically small punched out bone erosions, asymmetrically distributed, were the most characteristic finding; other notable changes were aseptic necrosis, tuft erosions, and periarticular calcification. Joint effusions were non-inflammatory, the cellular content was predominantly lymphocytic and the C3 level was normal. Most cases were controlled with non-steroidal anti-inflammatory agents and invariably responded to prednisone less than or equal to 7.5 mg/day.

摘要

对20例混合性结缔组织病患者进行了为期5年的随访。所有20例患者均出现关节炎,其中11例患者以此为首发症状。最常受累的关节为近端指间关节(PIP)、掌指关节(MCP)、腕关节、跖趾关节(MTP)和膝关节;其分布往往呈对称性,类似早期类风湿关节炎。6例患者出现关节畸形,但除1例毁形性关节炎患者外,未出现明显的功能障碍。放射学检查显示,最具特征性的表现是不对称分布的小的穿凿样骨侵蚀;其他显著变化包括无菌性坏死、指骨末端侵蚀和关节周围钙化。关节积液为非炎性,细胞成分以淋巴细胞为主,C3水平正常。大多数病例用非甾体抗炎药控制,对泼尼松剂量小于或等于7.5mg/天者均有反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2df7/1000265/b0062a619cfe/annrheumd00087-0003-a.jpg

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