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Primary systemic amyloidosis masquerading as giant cell arteritis. Case report and review of the literature.

Publication ,  Journal Article
Rao, JK; Allen, NB
Published in: Arthritis Rheum
March 1993

Amyloidosis is a rare disease in which a fibrillar protein is deposited in multiple human tissues. Of the 4 subtypes, the most common type involving rheumatic disease features is hemodialysis-associated amyloidosis. Herein we describe an elderly man who presented with symptoms of giant cell arteritis or systemic vasculitis and was found to have amyloidosis as demonstrated on muscle, nerve, and temporal artery biopsy.

Duke Scholars

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Published In

Arthritis Rheum

DOI

ISSN

0004-3591

Publication Date

March 1993

Volume

36

Issue

3

Start / End Page

422 / 425

Location

United States

Related Subject Headings

  • Temporal Arteries
  • Muscles
  • Male
  • Humans
  • Giant Cell Arteritis
  • Biopsy
  • Arthritis & Rheumatology
  • Amyloidosis
  • Amyloid
  • Aged
 

Citation

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Chicago
ICMJE
MLA
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Rao, J. K., & Allen, N. B. (1993). Primary systemic amyloidosis masquerading as giant cell arteritis. Case report and review of the literature. Arthritis Rheum, 36(3), 422–425. https://doi.org/10.1002/art.1780360320
Rao, J. K., and N. B. Allen. “Primary systemic amyloidosis masquerading as giant cell arteritis. Case report and review of the literature.Arthritis Rheum 36, no. 3 (March 1993): 422–25. https://doi.org/10.1002/art.1780360320.
Rao, J. K., and N. B. Allen. “Primary systemic amyloidosis masquerading as giant cell arteritis. Case report and review of the literature.Arthritis Rheum, vol. 36, no. 3, Mar. 1993, pp. 422–25. Pubmed, doi:10.1002/art.1780360320.
Journal cover image

Published In

Arthritis Rheum

DOI

ISSN

0004-3591

Publication Date

March 1993

Volume

36

Issue

3

Start / End Page

422 / 425

Location

United States

Related Subject Headings

  • Temporal Arteries
  • Muscles
  • Male
  • Humans
  • Giant Cell Arteritis
  • Biopsy
  • Arthritis & Rheumatology
  • Amyloidosis
  • Amyloid
  • Aged