Myopathy in primary systemic amyloidosis

Morie Gertz, Robert A. Kyle

Research output: Contribution to journalArticle

52 Citations (Scopus)

Abstract

Objective - To define the natural history of primary systemic amyloidosis when muscle involvement is prominent at presentation. Methods - A retrospective review was carried out of all patients seen at the tertiary referral practice of the Mayo Clinic between 1 January 1960 and 31 December 1994. All patients with primary systemic amyloidosis and proof of amyloid deposits by muscle biopsy were included for analysis. No patients were lost to follow up. Results - Twelve patients were identified with amyloidosis in muscle. Muscle involvement was the most prominent symptom in patients who had widespread visceral involvement, which included the heart, peripheral nerve, and tongue. Of the 12, three had skeletal muscle pseudohypertrophy. All patients had a demonstrable dysproteinaemia by the finding of free light chain in the serum or urine, a discrete monoclonal peak on serum or urine protein electrophoresis, or a monoclonal population of plasma cells in the bone marrow. Measurement of creatine kinase was not a useful test. Of eight patients treated with chemotherapy based on alkylating agents, three responded. The median survival for the entire group was 12 months. Conclusions - The finding of a monoclonal protein in a patient with muscle weakness is an important clue to the diagnosis of primary systemic amyloidosis. Most patients have visceral involvement outside the musculoskeletal system. A subset of patients seems to respond to systemic chemotherapy. The overall survival, however, remains poor, with most patients dying of cardiac failure. Immunoelectrophoresis of serum and urine should be a routine diagnostic test during the evaluation of myopathy of unknown cause.

Original languageEnglish (US)
Pages (from-to)655-660
Number of pages6
JournalJournal of Neurology Neurosurgery and Psychiatry
Volume60
Issue number6
DOIs
StatePublished - Jan 1 1996

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Muscular Diseases
Muscles
Urine
Primary amyloidosis
Serum
Drug Therapy
Musculoskeletal System
Immunoelectrophoresis
Survival
Alkylating Agents
Lost to Follow-Up
Muscle Weakness
Amyloid Plaques
Amyloidosis
Creatine Kinase
Plasma Cells
Natural History
Peripheral Nerves
Tongue
Routine Diagnostic Tests

Keywords

  • Multiple myeloma
  • Myopathy
  • Primary systematic amyloidosis

ASJC Scopus subject areas

  • Surgery
  • Clinical Neurology
  • Psychiatry and Mental health

Cite this

Myopathy in primary systemic amyloidosis. / Gertz, Morie; Kyle, Robert A.

In: Journal of Neurology Neurosurgery and Psychiatry, Vol. 60, No. 6, 01.01.1996, p. 655-660.

Research output: Contribution to journalArticle

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