Results 21 to 30 of about 17,240 (198)

Polymyositis following varicella and mumps infection in adults: report of two cases

Reumatismo, 2023
Idiopathic immune myopathies (IIMs) are autoimmune diseases caused by immune-mediated muscle damage. The etiology remains unclear. Epidemiological and experimental studies, both in animals and humans, hint at viruses as major environmental factors able ...
F. Masini, K. Gjeloshi, E. Pinotti, R. Ferrara, C. Romano, G. Cuomo   +5 more
doaj   +1 more source

Severe myopathy in a patient with chronic neurological disease – diagnostic challenges [PDF]

Romanian Journal of Rheumatology, 2023
Polymyositis is a rare disease that belongs to the idiopathic inflammatory myopathies (IIMs) group, characterized by chronic muscle inflammation, and in rare cases a life-threatening condition due to extra-muscular involvement.
Cristian-Mihai Ilie, Suzana Popescu, Sinziana Daia-Iliescu, Ioana Saulescu, Denisa Predeteanu, Violeta-Claudia Bojinca, Andra Balanescu, Daniela Opris-Belinski   +7 more
doaj   +1 more source

Chronic-graft-versus-host-disease-related polymyositis: a 17-months-old child with a rare and late complication of haematopoietic stem cell transplantation.

Mediterranean Journal of Hematology and Infectious Diseases, 2020
Background: Chronic graft versus host disease (cGVHD) occurs in 20-30% of paediatric patients receiving haemopoietic stem cell transplantation (HSCT). Neuromuscular disorders such as polymyositis are considered a rare and distinctive but non-diagnostic ...
Matteo Chinello, Rita Balter, Massimiliano De Bortoli, Virginia Vitale, Ada Zaccaron, Elisa Bonetti, Paola Tonin, Gaetano Vattemi, Valeria Guglielmi, Simone Cesaro   +9 more
doaj   +1 more source

High-Dose Subcutaneous Immunoglobulins for the Treatment of Severe Treatment-Resistant Polymyositis

Case Reports in Rheumatology, 2014
Polymyositis is a rare debilitating condition characterized by chronic inflammation and muscle weakness. Standard treatments include corticosteroids and immunosuppressants; however, resistance to these regimens may develop.
Cherin Patrick, Delain Jean-Christophe, Crave Jean-Charles, Cartry Odile   +3 more
doaj   +1 more source

Severe Rhabdomyolysis without Systemic Involvement: A Rare Case of Idiopathic Eosinophilic Polymyositis

Case Reports in Rheumatology, 2015
Introduction. Eosinophilic polymyositis (EPM) is a rare cause of rhabdomyolysis characterized by eosinophilic infiltrates in the muscle. We describe the case of a young patient with eosinophilic polymyositis causing isolated severe rhabdomyolysis without
Ayesha Farooq, Vivek Choksi, Andrew Chu, Dhruti Mankodi, Sameer Shaharyar, Keith O’Brien, Uday Shankar   +6 more
doaj   +1 more source

Myositis-specific and myositis-associated autoantibody profiles and their clinical associations in a large series of patients with polymyositis and dermatomyositis

Clinics, 2013
OBJECTIVE: To analyze the prevalence of myositis-specific and myositis-associated autoantibodies and their clinical correlations in a large series of patients with dermatomyositis/polymyositis.
Marcela Gran Pina Cruellas, Vilma dos Santos Trindade Viana, Maurício Levy-Neto, Fernando Henrique Carlos de Souza, Samuel Katsuyuki Shinjo   +4 more
doaj   +1 more source

Spontaneous Retroperitoneal Hemorrhage in a Mediastinal Tumor in a Patient With Polymyositis: A Case Report

Kaohsiung Journal of Medical Sciences, 2008
Spontaneous retroperitoneal hemorrhage is a lethal cause of acute abdomen that is most frequently related to drugs, coagulopathy and intra-abdominal tumors.
Tzu-Jung Fang, Shih-Chieh Hsu, Ming-Chen Shih, Cheng-Yuan Wang, Ling-I Chen, Yi-Chun Tsai, Yu-Chih Lin   +6 more
doaj   +1 more source

Case report: Systemic muscle involvement as the primary clinical manifestation of chronic active Epstein–Barr virus infection: A case-based review

Frontiers in Immunology, 2022
Chronic active Epstein–Barr virus infection (CAEBV) is common in Asian countries and characterized by recurrent or persistent infectious mononucleosis-like symptoms.
Shanfen Shi, Liangda Li, Cuiping Pan, Yandi Yang, Gun Chen, Yongping He   +5 more
doaj   +1 more source

Polymyositis.

The Hospital
Gema M. Lledó-Ibáñez, Jorge Álvarez Troncoso, Sergio Prieto-González   +2 more
  +5 more sources

Profiling of Myositis Specific Antibodies and Composite Scores as an Aid in the Differential Diagnosis of Autoimmune Myopathies

Diagnostics, 2021
(1) Background: Myositis specific antibodies (MSA) represent important diagnostic and stratification tools in idiopathic inflammatory myositis (IIM) patients.
Michael Mahler, Kishore Malyavantham, Andrea Seaman, Chelsea Bentow, Ariadna Anunciacion-Llunell, María Teresa Sanz-Martínez, Laura Viñas-Gimenez, Albert Selva-O’Callaghan   +7 more
doaj   +1 more source