臂颈炎性肌病的长期随访和肌肉影像学表现。

IF 7.5
Matteo Lucchini, Sara Bortolani, Mauro Monforte, Manuela Papacci, Enzo Ricci, Massimiliano Mirabella, Giorgio Tasca
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引用次数: 3

摘要

目的:报道一组诊断为肱颈炎性肌病(BCIM)的患者,特别关注肌肉MRI和随访数据。方法:回顾性评价诊断为BCIM的患者的临床、组织病理学、血清学和治疗前后的MRI表现。结果:6例患者均为女性,平均发病年龄为53岁(37-62岁)。平均诊断延迟为17个月,平均随访为35个月。最常见的临床特征包括主要累及颈部和上肢近端肌肉,其次是上肢远端、面部和球部肌肉的不同程度的无力。下肢受累是罕见的,尽管在严重的情况下存在。肌肉活检显示不同程度的血管周围和肌内膜炎症改变。所有患者均无肌炎特异性抗体,而抗核抗体均呈阳性;一半的患者有抗乙酰胆碱受体抗体,没有肌肉疲劳的迹象。MRI显示与下肢相比,上腰带和颈部肌肉受累不成比例,短tau反转恢复序列频繁出现高信号。大多数患者通过类固醇和免疫抑制剂治疗获得部分临床和放射学改善,特别是上肢近端肌肉,而颈部无力持续存在。结论:BCIM是一种炎症性肌病,具有特殊的临床和影像学表现,严重程度相对广泛。长期随访数据表明,适当的早期治疗可以预防慢性肌肉功能损害。MRI表征有助于减少诊断和治疗延误,对临床结果有积极影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy.

Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy.

Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy.

Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy.

Objective: To report on a cohort of patients diagnosed with brachio-cervical inflammatory myopathy (BCIM), with specific focus on muscle MRI and follow-up data.

Methods: Clinical, histopathologic, serologic, and pre- and post-treatment MRI findings of patients diagnosed with BCIM were retrospectively evaluated.

Results: Six patients, all females with a mean age at onset of 53 years (range 37-62 years), were identified. Mean diagnostic delay was 17 months, and mean follow-up was 35 months. Most common clinical features encompassed predominant involvement of neck and proximal upper limb muscles, followed by distal upper limb, facial, and bulbar muscle weakness with different severity. Lower limb involvement was rare, although present in severe cases. Muscle biopsies showed a heterogeneous degree of perivascular and endomysial inflammatory changes. Myositis-specific antibodies were absent in all patients, whereas all resulted positive for antinuclear antibodies; half of the patients had anti-acetylcholine receptor antibodies without evidence of muscle fatigability. MRI showed disproportionate involvement of upper girdle and neck muscles compared with lower limbs, with frequent hyperintensities on short-tau inversion recovery sequences. Partial clinical and radiologic improvement with steroid and immunosuppressant therapy was obtained in most patients, especially in proximal upper limb muscles, whereas neck weakness persisted.

Conclusion: BCIM is an inflammatory myopathy with a peculiar clinical and radiologic presentation and a relatively broad spectrum of severity. Long-term follow-up data suggest that appropriate and early treatment can prevent chronic muscle function impairment. MRI characterization can be helpful in reducing diagnostic and treatment delay with positive consequence on clinical outcome.

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