首页> 外文期刊>Southern Medical Journal >Juvenile dermatomyositis and polymyositis: a follow-up study of long-term sequelae.
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Juvenile dermatomyositis and polymyositis: a follow-up study of long-term sequelae.

机译:青少年皮肌炎和多发性肌炎:长期后遗症的随访研究。

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BACKGROUND. Juvenile dermatomyositis/polymyositis (DMS/PM) are childhood inflammatory myopathies that normally affect children between 2 and 15 years of age. The disease is manifested as severe proximal muscle weakness and, in JDMS, as a characteristic cutaneous eruption. It is difficult to predict the course of the disease. This study is aimed at objectively assessing the long-term morbidity of dermatomyositis/polymyositis in children. METHODS. Twelve cases of JDMS/PM identified through chart review were evaluated by physical and dermatologic examination, muscle testing, ultrasonography, and magnetic resonance imaging (MRI). RESULTS. The patient population included 6 male and 6 female patients with a mean age of 18.8 years (standard deviation 12.4). The mean age at onset of JDMS/PM was 5.8 years (SD 2.8), and the mean time from onset of symptoms to beginning of the study was 10.1 years (SD 9.3). The mean duration of corticosteroid therapy was 53.1 months (SD 40.5), with patients reporting an average of 1.7 relapses (SD 1.5). Patients compared their own activity level with that of healthy control subjects, and on a scale of 1 to 5 with 5 being normal, their mean score was 3.9 (SD 0.9). Fifty-eight percent of the patients had at least one residual finding on physical examination, and 78% of those with JDMS had residual dermatologic sequelae. Despite these findings, the mean grade for the group was 4.6 (SD 0.6) for muscle strength, using a scale of 0 to 5 with 0 being no muscle resistance and 5 being normal. In 60% of patients examined by ultrasonography, increased echogenicity indicated possible residual fibrotic change in at least one muscle group. Although MRI showed no active disease process in four patients, scattered intramuscular calcification was found in one patient. CONCLUSIONS. Multiple physical and dermatologic sequelae are commonly present in patients with JDMS/PM on long-term follow-up, but these do not preclude a productive life. Ultrasonography and MRI provide additional noninvasive means of analysis, but because of the current high cost, MRI is not routinely recommended.
机译:背景。少年皮肌炎/多发性肌炎(DMS / PM)是儿童炎症性肌病,通常会影响2至15岁的儿童。该疾病表现为严重的近端肌肉无力,在JDMS中表现为特征性的皮疹。很难预测疾病的进程。这项研究旨在客观评估儿童皮肌炎/多发性肌炎的长期发病率。方法。通过体检和皮肤病学检查,肌肉测试,超声检查和磁共振成像(MRI)对通过图表审查确定的12例JDMS / PM进行了评估。结果。该患者人群包括6名男性和6名女性患者,平均年龄为18.8岁(标准差为12.4)。 JDMS / PM发作的平均年龄为5.8岁(SD 2.8),从症状发作到研究开始的平均时间为10.1年(SD 9.3)。糖皮质激素治疗的平均持续时间为53.1个月(标准差40.5),患者报告平均复发1.7(标准差1.5)。患者将自己的活动水平与健康对照组的活动水平进行比较,以1到5的等级(其中5处于正常水平),他们的平均得分为3.9(SD 0.9)。 58%的患者在身体检查中至少有一个残留发现,而78%的JDMS患者具有残留的皮肤病后遗症。尽管有这些发现,该组的平均肌肉强度等级为4.6(SD 0.6),使用0到5的等级表示,0表示没有肌肉阻力,5表示正常。在超声检查中60%的患者中,回声增强表明至少一个肌肉组可能残留纤维化变化。尽管MRI显示4名患者未出现活动性疾病过程,但1名患者发现了分散的肌内钙化。结论。长期随访后,JDMS / PM患者通常会出现多种生理和皮肤后遗症,但这些并不排除生产寿命。超声检查和MRI提供了额外的非侵入性分析手段,但是由于当前成本高昂,因此不建议常规使用MRI。

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