نتایج جستجو برای: myositis

تعداد نتایج: 9008  

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...

2013
Melanie Neumann Susanne Krasemann Katharina Schröck Karin Steinbach Markus Glatzel

BACKGROUND In human and animal prion diseases, pathological prion protein, PrPSc, as well as prion infectivity is mainly found in the central nervous system, but also in lymphoid organs and muscle. Pathophysiology of prion colonization of lymphoid organs has been studied intensively, yet how myositis influences prion accumulation in muscle is unknown. RESULT We have investigated the influence...

2016
Pari Basharat

Idiopathic inflammatory myopathies (IIM) are traditionally identified as a group of disorders that target skeletal muscle due to autoimmune dysfunction. The IIM can be divided into subtypes based on certain clinical characteristics, and several classification schemes have been proposed. The predominant diagnostic criteria for IIM is the Bohan and Peter criteria, which subdivides IIM into primar...

Journal: :Reumatologia clinica 2017
Laura Nuño Beatriz Joven Patricia Carreira Valentina Maldonado Carmen Larena Irene Llorente Eva Tomero María Carmen Barbadillo Paloma García-de la Peña Lucía Ruiz Juan Carlos López-Robledillo Henry Moruno Ana Pérez Tatiana Cobo-Ibáñez Raquel Almodóvar Leticia Lojo Indalecio Monteagudo María Jesús García-De Yébenes Francisco Javier López-Longo

OBJECTIVE To analyze clinical characteristics, survival and causes of death of patients diagnosed with autoimmune inflammatory myositis in the REMICAM registry from the Society of Rheumatology in the Community of Madrid (SORCOM). METHODS Multicenter cohort of patients diagnosed with autoimmune inflammatory myopathy with follow-up between January 1980 and December 2014. A total of 313 variable...

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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