نتایج جستجو برای: autoimmune myositis

تعداد نتایج: 69470  

2012
David I. Stott Donna McIntyre

1.1 The B-cell response in autoimmune disease1 The pathological effects of autoimmune diseases on the target tissues can be mediated by autoantibodies, cell-mediated immune responses, or both. It is increasingly evident that some autoimmune diseases previously thought to be essentially T-cell-mediated also have a B-cell component, which may involve direct effects of autoantibody secreted by pla...

2016
Sevim Barbasso Helmers Xia Jiang David Pettersson Anna-Lis Wikman Pia Axelman Åsa Lundberg Ingrid E Lundberg Lars Alfredsson

OBJECTIVES To assess the association between inflammatory lung disease and the risk of developing idiopathic inflammatory myopathies. METHODS A population-based case-control study was conducted. Adult myositis cases, identified from the Swedish inpatient registry (diagnosed between 1995 and 1997), and randomly selected controls matched to cases on the date of birth, gender and residency, were...

2013
Latifa Tahiri Laila Chbani Siham Tizniti Abdelmajid Elmrini Taoufik Harzy

Myositis ossificans is a benign self limiting condition that usually related to trauma. Despite a clinically and histologically distinct entity, myositis ossificans still causes considerable difficulties in diagnosis. A 33-year-old Moroccan woman presented with a 2-month history of left inguinal inflammatory pain with limping gait, MRI examination suggested a malignant neoplasm such as soft tis...

Journal: :Diagnostic and interventional radiology 2009
Hasan Yiğit Ahmet Tuncay Turgut Pinar Koşar Hesna Müzeyyen Astarci Uğur Koşar

Proliferative myositis is a rare pseudosarcomatous inflammatory process. Radiological diagnosis of self-limiting proliferative myositis helps direct appropriate clinical management and avoiding unnecessary surgical excision. We present the ultrasonography, computed tomography, and magnetic resonance imaging findings in a case of proliferative myositis. In this case, malignancy was suspected, an...

Journal: :The Lancet. Neurology 2007
Merrilee Needham Frank L Mastaglia

Inclusion body myositis is the most common acquired muscle disease in older individuals, and its prevalence varies among countries and ethnic groups. The aetiology and pathogenesis of sporadic inclusion body myositis are still poorly understood; however genetic factors, ageing, and environmental triggers might all have a role. Unlike other inflammatory myopathies, sporadic inclusion body myosit...

2015
Jian Wei Yingwei Jia Bingsheng Liang

INTRODUCTION Myositis ossificans usually occurs in the vicinity of the elbow, knee joints, or hip joints, following obvious trauma or surgery. This is the first report on myositis ossificans of the serratus anterior. CASE PRESENTATION In this report we present a case of myositis ossificans within the serratus anterior which developed as a complication due to long-term nape massage. The patien...

Journal: :British medical journal 1984
R M Bernstein S H Morgan J Chapman C C Bunn M B Mathews M Turner-Warwick G R Hughes

An autoantibody known as anti-Jo-1 antibody is found in 25% of patients with myositis. Its prevalence in patients with both myositis and cryptogenic fibrosing alveolitis was 68% (13 out of 19 patients), compared with 7.5% in patients with myositis alone (four of 53) and 3% in patients with cryptogenic fibrosing alveolitis alone (two of 62). Anti-Jo-1 antibody may be useful in indicating patient...

2013
Sanam Verma Karen I Kroeker Richard N Fedorak

BACKGROUND Orbital myositis is a rare extra-intestinal manifestation of inflammatory bowel disease. Seventeen cases of Crohn's disease associated orbital myositis and 3 cases of ulcerative colitis associated orbital myositis have been reported in the published literature since 1970. We report the use of adalimumab (Abbott, Canada, Inc.) for orbital myositis in a patient with Crohn's disease who...

Journal: :Current opinion in rheumatology 2004
Gerald J D Hengstman Baziel G M van Engelen Walther J van Venrooij

PURPOSE OF REVIEW Defined autoantibodies are found in about half of the patients with myositis. Traditionally, these autoantibodies have been divided into myositis specific autoantibodies (MSAs) and myositis associated autoantibodies. Several studies have shown that MSAs are associated with specific clinical characteristics and can aid our understanding of the pathophysiology of myositis. REC...

Journal: :Archives of neurology 2000
A Mygland A Vincent J Newsom-Davis H Kaminski F Zorzato M Agius N E Gilhus J A Aarli

BACKGROUND About 50% of patients with thymoma have paraneoplastic myasthenia gravis (MG). Myositis and myocarditis or neuromyotonia (NMT) will also develop in some. Patients with thymoma-associated MG produce autoantibodies to a variety of neuromuscular antigens, particularly acetylcholine receptor (AChR), titin, skeletal muscle calcium release channel (ryanodine receptor [RyR]), and voltage-ga...

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