Primary systemic amyloidosis presenting as giant cell arteritis and polymyalgia rheumatica

Carlo Salvarani, Sherine E. Gabriel, Morie A. Gertz, Johannes Bjornsson, Chin Yang Li, Gene G. Hunder

Research output: Contribution to journalArticle

Abstract

Primary systemic amyloidosis may present with features suggesting a vasculitis, including giant cell arteritis (GCA) and polymyalgia rheumatica (PMR). In this report, we describe the clinical characteristics, temporal artery biopsy findings, and the response of vascular and musculoskeletal symptoms to corticosteroid therapy in 4 patients with primary systemic amyloidosis who presented with manifestations of GCA or PMR.

Original languageEnglish
Pages (from-to)1621-1626
Number of pages6
JournalArthritis and Rheumatism
Volume37
Issue number11
DOIs
Publication statusPublished - Nov 1994

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ASJC Scopus subject areas

  • Immunology
  • Rheumatology

Cite this

Salvarani, C., Gabriel, S. E., Gertz, M. A., Bjornsson, J., Li, C. Y., & Hunder, G. G. (1994). Primary systemic amyloidosis presenting as giant cell arteritis and polymyalgia rheumatica. Arthritis and Rheumatism, 37(11), 1621-1626. https://doi.org/10.1002/art.1780371111