AL amyloidosis presenting with limb girdle myopathy. Issue 6 (24th July 2018)

• Record Type: Journal Article
• Authors: Malek, Naveed; O'Donovan, Dominic G; Manji, Hadi
• Is Part Of: Practical neurology. Volume 18:Issue 6(2018)
• Page Start: 497
• Page End: 500
• Publication Date: 2018-07-24
• Subjects: myopathy -- amyloidosis; Neurology -- Periodicals; 616.8005
• DOI: 10.1136/practneurol-2018-001995
• Languages: English
• ISSNs: 1474-7758

Abstract

Abstract : An elderly Caucasian man presented with a 10-month history of proximal myopathy and dysphagia. His serum creatine kinase (CK) was elevated at 877 U/L (normal 40–320) and electromyography confirmed a myopathic process. Blood and urine tests suggested myeloma; bone marrow examination showed 30% plasma cells and stained positive for amyloid. The muscle biopsy was initially reported as normal but in the light of the bone marrow report, the biopsy specimen was stained for amyloid, which was positive. We diagnosed systemic amyloidosis causing a myopathy and have started treatment for myeloma.