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一例酷似双侧骨间后神经麻痹的混合性结缔组织病相关性肌炎病例。

A case of myositis associated with mixed connective tissue disease mimicking bilateral posterior interosseous nerve palsy.

作者信息

Inan Berin, Emet Abdulsamet, Odabasi Zeki

机构信息

Department of Neurology, Gulhane Medical Faculty, University of Health Sciences, Ankara, Turkey.

Department of Orthopedics and Traumatology, Etlik City Hospital, Ankara, Turkey.

出版信息

Ideggyogy Sz. 2025 May 30;78(5-6):211-213. doi: 10.18071/isz.78.0211.

Abstract

Overlap myositis (OM) is an idiopathic inflammatory myopathy characterized by proximal muscle weakness. However, atypical patterns of muscle involvement may also occur. We present a challenging case of OM mimicking bilateral posterior interosseous nerve (PIN) palsy. The patient presented with a gradual onset of bilateral finger drop over two years. Despite initial clinical suspicion of PIN palsy, electromyography revealed myopathic features. Laboratory assessments showed anti-ribonucleoprotein antibody positivity, with subsequent muscle biopsies supporting OM associated with mixed connective tissue disease. This case highlights the significance of considering atypical presentations of OM. Furthermore, it emphasizes the pivotal role of targeted muscle biopsies when initial biopsy results are inconclusive.

摘要

重叠性肌炎(OM)是一种以近端肌无力为特征的特发性炎性肌病。然而,也可能出现非典型的肌肉受累模式。我们报告一例具有挑战性的OM病例,该病例酷似双侧骨间后神经(PIN)麻痹。患者在两年内逐渐出现双侧手指下垂。尽管最初临床怀疑为PIN麻痹,但肌电图显示为肌病特征。实验室评估显示抗核糖核蛋白抗体阳性,随后的肌肉活检支持与混合性结缔组织病相关的OM。该病例突出了考虑OM非典型表现的重要性。此外,它强调了当初始活检结果不明确时,靶向肌肉活检的关键作用。

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