特发性炎性肌病的磁共振成像:解读肌肉受累模式。

IF 2.7 4区 医学 Q2 CLINICAL NEUROLOGY
S Sridhar , Saraswati Nashi , Karthik Kulanthaivelu , Seena Vengalil , Dipti Baskar , Kiran Polavarapu , Veeramani Preethish-Kumar , Hansashree Padmanabha , Mainak Bardhan , Gopikrishnan Unnikrishnan , Akshata Huddar , Deepak Menon , Vidya Nittur , Manoj Rajanna , Nandeesh Bevinahalli , Aneesha Thomas , Muddasu Suhasini Keerthipriya , Yashwanth Gangadhar , P V Pratyusha , Jitender Saini , Atchayaram Nalini
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引用次数: 0

摘要

特发性炎症性肌病(IIMs)是一组免疫介导的疾病,影响肌肉。我们的研究旨在探讨IIM亚群中肌肉受累的具体模式。进行了一项双视角观察性研究。评估包括125例IIM患者的临床特征,MMT8量表,MDAAT,分别使用改良Stramare(分级1-5)和改良Goutallier-Lamminen-Mercuri (GLM)评分对肌肉MRI进行水肿/脂肪替代严重程度评估。125例患者被分为四个亚组:皮肌炎(DM)、免疫介导的坏死性肌病(IMNM)、重叠肌炎(OM)和血清阴性组。就诊时的中位年龄为35岁。中位病程为8个月。DM中,53.12%的患者内收肌组出现3 ~ 5级水肿。在腿部,46.8%的患者表现为下肢深屈肌及腓骨3-5级水肿,65.6%的患者表现为明显的筋膜炎。在IMNM中,52.1%的患者表现为股直肌和半膜肌4-5级水肿。有趣的是,在腿部,78.2%的IMNM患者没有腓骨水肿。对于OM亚组,没有特定的受累模式。在血清阴性亚群中,股外侧肌表现为4-5级水肿,而在腿部,深后腔室和腓肌群表现为轻微至无水肿。小腿腓骨肌受累是糖尿病的一个特征性特征,在其他亚组中明显幸免。除IMNM外,所有组均观察到轻度肌肉脂肪替代,其中IMNM更为明显。该研究拓宽了炎性肌炎的成像频谱,并引入了选择性受累肌肉的创新概念。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Magnetic resonance imaging in idiopathic inflammatory myopathies: deciphering the pattern of muscle involvement

Magnetic resonance imaging in idiopathic inflammatory myopathies: deciphering the pattern of muscle involvement
Idiopathic inflammatory myopathies (IIMs) constitute a group of immune-mediated disorders, affecting muscles. Our study aims to investigate the specific patterns of muscle involvement in subgroups of IIM. An ambispective and observational study was conducted. The evaluation encompassed clinical characterization, scales of MMT8, MDAAT, assessment of severity of edema/ fatty replacement using Modified Stramare (grades 1-5) & Modified Goutallier-Lamminen-Mercuri (GLM) scores, respectively on the muscle MRI of 125 patients with IIM. A total of 125 patients were categorized into four subgroups: dermatomyositis (DM), immune- mediated necrotizing myopathy (IMNM), overlap myositis (OM), & seronegative groups. Median age at presentation was 35 years. Median duration of illness was 8 months. In DM, 53.12% of patients showed grade 3 to grade 5 edema in adductor group. In the leg, 46.8% showed grade 3-5 edema in the deep flexors of leg & peronei, and 65.6% had significant fasciitis. In IMNM, 52.1% displayed grade 4-5 edema in rectus femoris & semimembranosus. Interestingly, in the leg, 78.2% of IMNM patients lacked edema in peroneii. For OM subgroup, there was no specific pattern of involvement. In seronegative subset, vastus lateralis showed grade 4-5 edema, while in the leg, deep posterior compartment and peroneal muscle group exhibited subtle to no edema. The involvement of peroneus muscles in leg emerged as a characteristic feature of DM, they were conspicuously spared in other subgroups. Mild muscle fatty replacement was observed in all groups except for IMNM, where it was more pronounced. The research broadens the imaging spectrum of inflammatory myositis & introduces innovative concepts of selective involvement of muscles.
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来源期刊
Neuromuscular Disorders
Neuromuscular Disorders 医学-临床神经学
CiteScore
4.60
自引率
3.60%
发文量
543
审稿时长
53 days
期刊介绍: This international, multidisciplinary journal covers all aspects of neuromuscular disorders in childhood and adult life (including the muscular dystrophies, spinal muscular atrophies, hereditary neuropathies, congenital myopathies, myasthenias, myotonic syndromes, metabolic myopathies and inflammatory myopathies). The Editors welcome original articles from all areas of the field: • Clinical aspects, such as new clinical entities, case studies of interest, treatment, management and rehabilitation (including biomechanics, orthotic design and surgery). • Basic scientific studies of relevance to the clinical syndromes, including advances in the fields of molecular biology and genetics. • Studies of animal models relevant to the human diseases. The journal is aimed at a wide range of clinicians, pathologists, associated paramedical professionals and clinical and basic scientists with an interest in the study of neuromuscular disorders.
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