Giladi Michael, Maman Eran, Paran Daphna, Bickels Jacob, Comaneshter Doron, Avidor Boaz, Varon-Graidy Merav, Ephros Moshe, Wientroub Shlomo
Pridan Laboratory for Molecular Biology of Infectious Diseases, Ichilov Hospital, Tel-Aviv Sourasky Medical Center, 6 Weizman Street, Tel-Aviv 64239, Israel.
Arthritis Rheum. 2005 Nov;52(11):3611-7. doi: 10.1002/art.21411.
To characterize the articular manifestations of cat-scratch disease (CSD) and to evaluate the long-term clinical outcome of those manifestations.
A community- and hospital-based surveillance study of CSD was conducted in Israel between 1991 and 2002. CSD was defined as present in a patient when a compatible clinical syndrome and a positive confirmatory finding of Bartonella henselae (by serology and/or polymerase chain reaction) were identified. CSD patients with arthropathy (arthritis/arthralgia) that limited or precluded usual activities of daily living constituted the study group. Patients were followed up until > or =6 weeks after resolution of symptoms, or if symptoms persisted, for >/=12 months. CSD patients without arthropathy served as controls.
Among 841 CSD patients, 24 (2.9%) had rheumatoid factor-negative arthropathy that was often severe and disabling. Both univariate and multivariate analyses identified female sex (67% of arthropathy patients versus 40% of controls; relative risk [RR] 2.5, P = 0.047), age older than 20 years (100% of arthropathy patients versus 43% of controls; RR 4.9, P = 0.001), and erythema nodosum (21% of arthropathy patients versus 2% of controls; RR 7.9, P = 0.001) as variables significantly associated with arthropathy. Knee, wrist, ankle, and elbow joints were most frequently affected. Ten patients (42%) had severe arthropathy in the weight-bearing joints, which substantially limited their ability to walk, and 4 of these patients were hospitalized. All of the patients had regional lymphadenopathy, 37.5% had nocturnal joint pain, and 25% had morning stiffness. Nineteen patients (79.2%) recovered after a median duration of 6 weeks (range 1-24 weeks), whereas 5 patients (20.8%) developed chronic disease persisting 16-53 months (median 30 months) after the onset of arthropathy.
This is the first comprehensive study of arthropathy in CSD. CSD-associated arthropathy is an uncommon syndrome affecting mostly young and middle-age women. It is often severe and disabling, and may take a chronic course.
描述猫抓病(CSD)的关节表现,并评估这些表现的长期临床结局。
1991年至2002年在以色列开展了一项基于社区和医院的CSD监测研究。当患者出现符合的临床综合征且巴尔通体(通过血清学和/或聚合酶链反应)确诊结果呈阳性时,定义为患有CSD。患有影响或妨碍日常生活正常活动的关节病(关节炎/关节痛)的CSD患者构成研究组。对患者进行随访,直至症状缓解后≥6周,或如果症状持续,则随访≥12个月。无关节病的CSD患者作为对照。
在841例CSD患者中,24例(2.9%)患有类风湿因子阴性的关节病,通常较为严重且导致残疾。单因素和多因素分析均确定女性(关节病患者中的67% 对比对照组中的40%;相对风险[RR] 2.5,P = 0.047)、年龄大于20岁(关节病患者中的100% 对比对照组中的43%;RR 4.9,P = 0.001)和结节性红斑(关节病患者中的21% 对比对照组中的2%;RR 7.9,P = 0.001)为与关节病显著相关的变量。膝关节、腕关节、踝关节和肘关节最常受累。10例患者(42%)在负重关节出现严重关节病,严重限制了他们的行走能力,其中4例患者住院治疗。所有患者均有局部淋巴结病,37.5%有夜间关节痛,25%有晨僵。19例患者(79.2%)在中位病程6周(范围1 - 24周)后康复,而5例患者(20.8%)在关节病发作后发展为慢性病,持续16 - 53个月(中位30个月)。
这是首次对CSD关节病进行的全面研究。CSD相关关节病是一种罕见综合征,主要影响中青年女性。它通常较为严重且导致残疾,可能呈慢性病程。