Document Detail


Primary systemic amyloidosis presenting as giant cell arteritis and polymyalgia rheumatica.
MedLine Citation:
PMID:  7980674     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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.
Authors:
C Salvarani; S E Gabriel; M A Gertz; J Bjornsson; C Y Li; G G Hunder
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Arthritis and rheumatism     Volume:  37     ISSN:  0004-3591     ISO Abbreviation:  Arthritis Rheum.     Publication Date:  1994 Nov 
Date Detail:
Created Date:  1994-12-02     Completed Date:  1994-12-02     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  0370605     Medline TA:  Arthritis Rheum     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  1621-6     Citation Subset:  AIM; IM    
Affiliation:
Mayo Clinic and Foundation, Rochester, Minnesota 55905.
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MeSH Terms
Descriptor/Qualifier:
Aged
Amyloidosis / complications*,  diagnosis,  drug therapy
Biopsy
Female
Giant Cell Arteritis / etiology*,  pathology
Humans
Intermittent Claudication / etiology
Male
Polymyalgia Rheumatica / etiology*
Prednisone / therapeutic use
Temporal Arteries / pathology
Chemical
Reg. No./Substance:
53-03-2/Prednisone
Comments/Corrections
Comment In:
Arthritis Rheum. 1996 Jun;39(6):1073-4   [PMID:  8651977 ]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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