Results 71 to 80 of about 16,326 (177)
Polymyositis and the Spectrum of Scleroderma Disorders [PDF]
Polymyositis (PM) is usually associated to other autoimmune or connective tissue diseases. The authors report the case of a 59-year-old man with pulmonary fibrosis, who presented with constitutional symptoms and gradually developed proximal muscle ...
Madaleno, João +9 more
core +1 more source
Fibromyalgia in the Setting of Prior Epstein–Barr Virus Infection: A Case Report
ABSTRACT Accurate diagnosis of fibromyalgia requires careful consideration of overlapping conditions. This case underscores the role of Epstein–Barr virus (EBV) serology in patients with persistent fatigue and pain, while illustrating the challenges of diagnosing fibromyalgia amid concurrent health problems.
Saachi Bhattessa, Tirth Dave, Priti Modi
wiley +1 more source
Diagnosis dan Tatalaksana Polymyositis
Polymyositis adalah miopati inflamasi idiopatik yang menyebabkan kelemahan otot simetris proksimal, peningkatan kadar enzim otot rangka, serta elektromiografi (EMG) dan temuan biopsi otot yang spesifik.
Yonata, Ade
core
ABSTRACT Background Pembrolizumab, an anti‐PD‐1 immune checkpoint inhibitor, has transformed the treatment of multiple solid tumors. However, it can rarely cause immune‐related myositis, which may involve limb, bulbar, and respiratory muscles, posing a risk of severe morbidity and mortality. Early recognition and management are essential. We report two
Francesca Rifaldi +5 more
wiley +1 more source
Walsh & Hoyt: Polymyositis and Dermatomyositis
Polymyositis is an inflammatory myopathy that affects striated skeletal muscle and, less commonly, cardiac muscle. The diagnosis of polymyositis is based on the presence of at least two of the following: 1. Proximal muscle weakness. 2.
Daniel M. Jacobson, MD (1956-2003); Howard D. Pomeranz, MD
core +1 more source
Pathogenesis of muscle weakness in inflammatory myositis
Idiopathic inflammatory myositis (IIM) is a heterogeneous group of autoimmune diseases. These are characterized by muscle weakness and fatigue along with other systemic manifestations, ranging from pulmonary alveolitis to vasculopathic ulcers.
Sai Kumar Dunga +2 more
doaj +1 more source
Myocardial fibrosis in polymyositis
Myocardial involvement in polymyositis is commonly suspected in noninvasive studies, but symptomatic cardiac disease is rare. We describe a 27-year-old woman with a 6 year history of severe polymyositis and persistent elevation of creatine phosphokinase ...
Kruger, K. +3 more
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Deep learning–based analysis of human skeletal muscle histology identifies increased nuclear size and altered nuclear number as robust features of aging. These morphometric changes associate with coordinated transcriptional programs and support a scalable, tissue‐level biomarker framework for muscle aging, validated in inflammatory myopathy cohorts ...
Tam Dao +13 more
wiley +1 more source
Yanqing Li,1 Peihong Wang,2 Lei Li,3 Fei Wang,4 Yuxiu Liu5 1Department of Pharmacy Intravenous Admixture Services, Affiliated Hospital of Weifang Medical University, Weifang, 2Department of Interventional Oncology, Weifang Tumor Hospital, Weifang ...
Liu Y, Li Y, Wang P, Wang F, Li L
core
Carbamoyl phosphate synthetase 1 (CPS1) deficiency (OMIM#237300) is a rare inherited disorder due to complete or partial lack of the CPS1 enzyme. Polymyositis is a relatively rare systemic inflammatory autoimmune disease.
Kazuhiro Yokota +8 more
doaj +1 more source

