Abstract

ObjectivesTo evaluate the value of whole-body magnetic resonance imaging (WBMRI) in diagnosing muscular and extra muscular lesions in patients with polymyositis (PM) and dermatomyositis (DM).MethodsA retrospective analysis of WBMRI data from PM/DM patients who met the Bohan and Peter diagnostic criteria was performed. X2 test was used to compare the rate of positive diagnosis of newly diagnosed patients using WBMRI, serum creatine kinase test, and EMG. McNemar test was used to compare the performance of WBMRI and chest CT in detecting interstitial lung disease (ILD).ResultsThe study included 129 patients (30 PM cases and 99 DM cases). Of them, 81.4% (105/129) showed a visible inflammatory muscular edema on their WBMRI; 29.5% (38/129) had varying degrees of fatty infiltration (9 cases with clear muscular atrophy). Of the 66 newly diagnosed patients, the positive rates of WBMRI, muscle biopsy, serum creatine kinase test and EMG were 86.4% (57/66), 92.4% (61/66), 71.2% (47/66) and 71.1% (32/45), respectively. There was no significant difference in the positive rates between WBMRI and muscle biopsy (X2 = 1.28, P = 0.258). The WBMRI had a higher positive rate than both serum creatine kinase test (X2 = 4.53, P = 0.033) and EMG (X2 = 3.92, P = 0.047). In addition to muscular changes, WBMRI also detected interstitial lung disease (ILD) in 38 cases (29.5%), osteonecrosis in 15 cases (11.6%), and neoplastic lesions (5 malignant; 7 benign) in 12 cases (9.3%). Of the 61 patients who underwent routine chest CT examinations, the WBMRI and CT revealed ILD in 29 cases and 35 cases respectively. There was no significant difference in the sensitivity between WBMRI and CT (p = 0.146).ConclusionsWBMRI is a sensitive, non-invasive and efficient imaging method. It comprehensively displays the extent of muscular involvement in PM/DM patients, and it has the ability to diagnose other associated extra muscular diseases, such as ILD and systemic malignancy. WBMRI can also help screen steroid-induced osteonecrosis.

Highlights

  • Polymyositis (PM) and dermatomyositis (DM) fall into the class of idiopathic inflammatory myopathies, a group of autoimmune diseases characterized by inflammatory changes of the skeletal muscle [1]

  • There was no significant difference in the positive rates between whole-body magnetic resonance imaging (WBMRI) and muscle biopsy (X2 = 1.28, P = 0.258)

  • Of the 61 patients who underwent routine chest CT examinations, the WBMRI and CT revealed interstitial lung disease (ILD) in 29 cases and 35 cases respectively

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Summary

Introduction

Polymyositis (PM) and dermatomyositis (DM) fall into the class of idiopathic inflammatory myopathies, a group of autoimmune diseases characterized by inflammatory changes of the skeletal muscle [1]. Magnetic resonance imaging (MRI) is a noninvasive examination which has no ionizing radiation and can scan a large range of the body. Conventional MRI usually includes limited scanning of the proximal lower limb muscle girdle or scanning of the proximal upper limb girdle. There have been reports that demonstrate the success of whole-body magnetic resonance imaging (WBMRI) through short tau inversion recovery (STIR) sequence in the diagnosis of PM / DM [7,8,9]. WBMRI has the advantage of documenting inflammatory myopathy of the whole body, including the psoas, intercostal, and neck muscles, which can not be done by conventional MRI

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