Unusual features of myositis with amyloid myopathy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Neurology (clinical),Dermatology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s10072-022-06538-2.pdf
Reference5 articles.
1. Spuler S, Emslie-Smith A, Engel AG (1998) Amyloid myopathy: an underdiagnosed entity. Ann Neurol 43:719–728
2. Tanabe H, Maki Y, Urabe S, Higuchi I, Obayashi K, Hokezu Y (2015) Myopathy in a patient with systemic AA amyloidosis possibly induced by psoriasis vulgaris: an autopsy case: myopathy in systemic AA Amyloidosis. Muscle Nerve 52:1113–1117
3. Moore S, Symmons DP, DuPlessis D, Chinoy H (2015) Amyloid myopathy masquerading as polymyositis. Clin Exp Rheumatol Italy 33:590–591
4. Müller AMS, Geibel A, Neumann HPH et al (2006) Primary (AL) Amyloidosis in plasma cell disorders. Oncologist 11:824–830
5. Pestronk A, Choksi R (2021) Pathology features of immune and inflammatory myopathies, including a polymyositis pattern, relate strongly to serum autoantibodies. J Neuropathol Exp Neurol 80:812–820
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