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[炎症性肌肉疾病的肌超声检查结果]

[Myosonographic findings in inflammatory muscular diseases].

作者信息

Reimers C D

机构信息

Friedrich Baur-Institut, Klinikum Innenstadt, Ludwig-Maximilians-Universität, München.

出版信息

Z Rheumatol. 1993 Mar-Apr;52(2):105-9.

PMID:8517071
Abstract

Inflammatory myopathies are rare diseases with an annual incidence of about 1-8 per 1 million persons. However, they are of special importance in myology as they can be treated successfully. There are auto-immune mediated and infectious forms of myositis. From the clinical and myopathological view, one can distinguish acute and chronic forms: the former presenting with distinct inflammatory reactions in the muscle tissue and often causing myalgia. Muscle atrophy, the latter presenting with marked muscle weakness, often with clear muscle atrophy and mesenchymal abnormalities in the biopsy. Ultrasound well documents muscle atrophy, sometimes compensatory hypertrophy, as well as mesenchymal abnormalities such as lipomatosis and fibrosis. In very acute myositis, as in pyomyositis muscle edema and abscesses can be depicted. Typical findings in autoimmune mediated myositis are reported based on our own experiences in 75 patients and according to the literature. The degree and distribution of muscle atrophy and mesenchymal abnormalities visualized by ultrasound can give clues to the type and prognosis regarding muscle function. Additionally, ultrasound can be used for searching the optimal biopsy site.

摘要

炎性肌病是罕见疾病,年发病率约为每100万人中有1 - 8例。然而,它们在肌病学中具有特殊重要性,因为可以成功治疗。肌炎有自身免疫介导型和感染型。从临床和肌病理角度来看,可以区分急性和慢性形式:前者在肌肉组织中表现出明显的炎症反应,常引起肌痛。后者表现为明显的肌肉无力,活检时通常伴有明显的肌肉萎缩和间充质异常。超声能很好地记录肌肉萎缩,有时还有代偿性肥大,以及间充质异常,如脂肪瘤病和纤维化。在非常急性的肌炎中,如脓性肌炎,可显示肌肉水肿和脓肿。基于我们对75例患者的自身经验并根据文献报道了自身免疫介导性肌炎的典型表现。超声显示的肌肉萎缩程度和分布以及间充质异常可为肌肉功能的类型和预后提供线索。此外,超声可用于寻找最佳活检部位。

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