Dermatomyositis

A type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness.

Necrotizing myopathy



Total: 7

                       


(per page)
PMID (PMCID)
28414153
 MIXED_SAMPLE Adult
Inflammatory myopathy associated with myasthenia gravis with and without thymic pathology: Report of four cases and literature review.
Santos E, Coutinho E, Martins da Silva A, Marinho A, Vasconcelos C, Taipa R, Pires MM, Goncalves G, Lopes C, Leite MI.
Autoimmun Rev. 2017;16(6):644-649.
Case 1: MG, polymyositis and thymolipoma; case 2: MG and necrotizing myopathy without thymic pathology on a background of scleroderma, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, telangiectasia (CREST); case 3: MG and dermatomyositis without thymic pathology; case 4: MG and dermatomyositis with type C thymoma.
28414153
 MIXED_SAMPLE Adult
Inflammatory myopathy associated with myasthenia gravis with and without thymic pathology: Report of four cases and literature review.
Santos E, Coutinho E, Martins da Silva A, Marinho A, Vasconcelos C, Taipa R, Pires MM, Goncalves G, Lopes C, Leite MI.
Autoimmun Rev. 2017;16(6):644-649.
Case 1: MG, polymyositis and thymolipoma; case 2: MG and necrotizing myopathy without thymic pathology on a background of scleroderma, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, telangiectasia (CREST); case 3: MG and dermatomyositis without thymic pathology; case 4: MG and dermatomyositis with type C thymoma.
22198662
 FEMALE
Paraneoplastic necrotizing myopathy and dermatomyositis in a patient with rectosigmoid carcinoma.
Samuels N, Applbaum YH, Esayag Y.
Rheumatol Int. 2013;33(6):1619-21.
Paraneoplastic necrotizing myopathy and dermatomyositis in a patient with rectosigmoid carcinoma.
19813188
 MIXED_SAMPLE Middle Aged
Immune-mediated necrotizing myopathy associated with statins.
Grable-Esposito P, Katzberg HD, Greenberg SA, Srinivasan J, Katz J, Amato AA.
Muscle Nerve. 2010;41(2):185-90.
Exposure to statins prior to onset was significantly higher in patients with necrotizing myopathy (82%) as compared to those with dermatomyositis (18%), polymyositis (24%), and inclusion-body myositis (38%) seen in the same time period.
18068861
 MIXED_SAMPLE Adult
Diagnostic uncertainty in the inflammatory myopathies.
Verity MA.
Best Pract Res Clin Rheumatol. 2007;21(6):1051-70.
Differential diagnostic possibilities are considered in presentations of idiopathic polymyositis, statin myotoxicity, the inflammatory component with the dysferlinopathies, treated dermatomyositis, a necrotizing myopathy with pipe-stem microvascular change, an inflammatory myopathy with abundant macrophages, inclusion-body myositis, and the differential diagnosis of problems with eosinophilic infiltration in the muscle biopsy.
8628498
 MALE Middle Aged
Necrotizing myopathy with pipestem capillaries and minimal cellular infiltration: a case associated with cutaneous signs of dermatomyositis.
Authier FJ, Kondo H, Ghnassia RT, Revuz J, Gherardi RK.
Neurology. 1996;46(5):1448-51.
We describe a patient with exercise-dependent painful myopathy related to a necrotizing myopathy with pipestem capillaries in whom mild cutaneous signs of dermatomyositis were detected 7 years after onset and who subsequently developed multiple cerebral infarcts.
8628498
 MALE Middle Aged
Necrotizing myopathy with pipestem capillaries and minimal cellular infiltration: a case associated with cutaneous signs of dermatomyositis.
Authier FJ, Kondo H, Ghnassia RT, Revuz J, Gherardi RK.
Neurology. 1996;46(5):1448-51.
Necrotizing myopathy with pipestem capillaries and minimal cellular infiltration: a case associated with cutaneous signs of dermatomyositis.