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首页> 外文期刊>The Israel Medical Association journal: IMAJ >Diagnostic workup for mixed connective tissue disease in childhood.
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Diagnostic workup for mixed connective tissue disease in childhood.

机译:儿童混合性结缔组织病的诊断检查。

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摘要

Raynaud's phenomenon, fatigue and pain (myalgia and arthralgia) are important presenting symptoms of pediatric-onset mixed connective tissue disease. The difficulty is that many adolescent girls complain of pain along with fatigue without evidence for serious disease. However, in patients with Raynaud's phenomenon one should search for evidence of connective tissue diseases. Capillaroscopy could be helpful since capillary changes of the SD-type significantly correlate with future development of scleroderma spectrum disorders. Symptoms of MCTD change in most patients during the disease course: in general the inflammatory features that are also seen in systemic lupus erythematosus and juvenile dermatomyositis have the tendency to disappear over years, but Raynaud's phenomenon is persistent and scleroderma symptoms become progressively prominent. Long-lasting remission occurs only in a minority of patients, while the majority has mild disease activity. Mortality in children with MCTD is lower than in adults. Since a change of symptoms is in the nature of the disease, a thorough and frequent evaluation of children with (probable) MCTD is important to detect organ involvement, which should be treated at an early (pre-symptomatic) stage. We present a diagnostic workup scheme for children and adolescents with propable MCTD.
机译:雷诺现象,疲劳和疼痛(肌痛和关节痛)是小儿发作性混合性结缔组织病的重要症状。困难在于许多青春期女孩抱怨疼痛和疲劳,而没有严重疾病的证据。但是,对于患有雷诺现象的患者,应该寻找结缔组织疾病的证据。毛细血管镜检查可能会有所帮助,因为SD型的毛细血管变化与硬皮病谱的发展密切相关。 MCTD的症状在疾病过程中大多数患者中发生变化:通常,系统性红斑狼疮和青少年皮肌炎中也见到的炎症特征会随着时间的流逝而消失,但雷诺现象仍持续存在,硬皮病症状逐渐突出。持久缓解仅在少数患者中发生,而大多数患者具有轻度疾病活动。 MCTD患儿的死亡率低于成人。由于症状的改变是疾病的本质,因此对(可能)MCTD患儿进行全面,频繁的评估对于检测器官受累很重要,应在早期(症状发生前)对其进行治疗。我们提出了适用于MCTD的儿童和青少年的诊断性检查方案。

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