{"title":"特发性炎性肌病的磁共振成像:解读肌肉受累模式。","authors":"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","doi":"10.1016/j.nmd.2024.105257","DOIUrl":null,"url":null,"abstract":"<div><div>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.</div></div>","PeriodicalId":19135,"journal":{"name":"Neuromuscular Disorders","volume":"47 ","pages":"Article 105257"},"PeriodicalIF":2.7000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Magnetic resonance imaging in idiopathic inflammatory myopathies: deciphering the pattern of muscle involvement\",\"authors\":\"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\",\"doi\":\"10.1016/j.nmd.2024.105257\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>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.</div></div>\",\"PeriodicalId\":19135,\"journal\":{\"name\":\"Neuromuscular Disorders\",\"volume\":\"47 \",\"pages\":\"Article 105257\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Neuromuscular Disorders\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S096089662401753X\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuromuscular Disorders","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S096089662401753X","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
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.
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.