Maman Eran, Bickels Jacob, Ephros Moshe, Paran Daphna, Comaneshter Doron, Metzkor-Cotter Einat, Avidor Boaz, Varon-Graidy Merav, Wientroub Shlomo, Giladi Michael
Department of Pediatric Orthopaedics, Dana Children's Hospital.
Clin Infect Dis. 2007 Dec 15;45(12):1535-40. doi: 10.1086/523587.
Musculoskeletal manifestations (MMs) are considered to be rare in cat scratch disease (CSD) and are not well characterized. We aimed to study MMs of CSD.
A surveillance study performed over 11 years identified patients with CSD on the basis of compatible clinical presentation and confirmatory serological test or PCR results for Bartonella henselae. Patients with CSD who had MMs (i.e., myalgia, arthritis, arthralgia, tendinitis, osteomyelitis, and neuralgia) were compared with patients with CSD who did not have MMs (control subjects).
Of 913 patients with CSD, 96 (10.5%) had MMs. Myalgia (in 53 patients [5.8%]) was often severe, with a median duration of 4 weeks (range, 1-26 weeks). Arthropathy (arthralgia and/or arthritis; in 50 patients [5.5%]) occurred mainly in the medium and large joints and was classified as moderate or severe in 26 patients, with a median duration of 5.5 weeks (range, 1-240 weeks). In 7 patients, symptoms persisted for >or=1 year; 5 developed chronic disease. Tendinitis, neuralgia, and osteomyelitis occurred in 7, 4, and 2 patients, respectively. Patients with MMs were significantly older than patients in the control group (median age, 31.5 years vs. 15.0 years). In multivariate analysis, age >20 years was associated with having any MM (relative risk [RR], 4.96; 95% confidence interval [CI], 2.79-8.8), myalgia (RR, 4.69; 95% CI, 2.22-9.88), and arthropathy (RR, 11.0; 95% CI, 4.3-28.2). Arthropathy was also associated with female sex (RR, 1.89; 95% CI, 1.01-3.52) and erythema nodosum (RR, 4.07; 95% CI, 1.38-12.02).
MMs of CSD are more common than previously thought and affect one-tenth of patients with CSD. MMs occur mostly in patients aged >20 years and may be severe and prolonged. Osteomyelitis, the most well known MM of CSD is, in fact, the rarest.
肌肉骨骼表现(MMs)在猫抓病(CSD)中被认为较为罕见,且特征尚不明确。我们旨在研究CSD的MMs。
一项为期11年的监测研究,根据兼容的临床表现以及针对汉赛巴尔通体的血清学确诊试验或PCR结果来确定CSD患者。将出现MMs(即肌痛、关节炎、关节痛、肌腱炎、骨髓炎和神经痛)的CSD患者与未出现MMs的CSD患者(对照组)进行比较。
在913例CSD患者中,96例(10.5%)出现了MMs。肌痛(53例患者[5.8%])通常较为严重,中位持续时间为4周(范围1 - 26周)。关节病(关节痛和/或关节炎;50例患者[5.5%])主要发生在中大型关节,26例患者被归类为中度或重度,中位持续时间为5.5周(范围1 - 240周)。7例患者症状持续≥1年;5例发展为慢性病。肌腱炎、神经痛和骨髓炎分别发生在7例、4例和2例患者中。出现MMs的患者比对照组患者年龄显著更大(中位年龄31.5岁对15.0岁)。在多变量分析中,年龄>20岁与出现任何MMs相关(相对风险[RR],4.96;95%置信区间[CI],2.79 - 8.8)、肌痛(RR,4.69;95% CI,2.22 - 9.88)以及关节病(RR,11.0;95% CI,4.3 - 28.2)。关节病还与女性性别(RR,1.89;95% CI,1.01 - 3.52)和结节性红斑(RR,4.07;95% CI,1.38 - 12.02)相关。
CSD的MMs比之前认为的更为常见,影响十分之一的CSD患者。MMs大多发生在年龄>20岁的患者中,可能严重且持续时间长。骨髓炎作为CSD最广为人知的MMs,实际上是最罕见的。