Literature DB >> 21312024

[Facial edema as an earlier presenting sign of giant cell arteritis. Possible relationship with angioedema].

G Bahat1, S Akin, F Tufan, A Gelincik, N Erten, M A Karan.   

Abstract

Giant cell arteritis (GCA) is a chronic granulomatous vasculitis of unknown etiology occurring in the elderly. New-onset headache, scalp tenderness, jaw claudication, temporal artery abnormalities on physical examination, visual symptoms and associated polymyalgia rheumatica represent the most typical and frequent features of the disease. However, facial edema is being more commonly recognized as a presenting symptom that may herald the disease. We present a case with facial edema as initial symptom and discuss if this rare symptom of GCA is due to hereditary or acquired angioedema.

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Year:  2011        PMID: 21312024     DOI: 10.1007/s00393-010-0702-5

Source DB:  PubMed          Journal:  Z Rheumatol        ISSN: 0340-1855            Impact factor:   1.372


  16 in total

Review 1.  C1 inhibitor deficiency: hereditary and acquired forms.

Authors:  A P Kaplan
Journal:  J Investig Allergol Clin Immunol       Date:  2001       Impact factor: 4.333

Review 2.  C1-inhibitor: an anti-inflammatory reagent with therapeutic potential.

Authors:  M Kirschfink; T E Mollnes
Journal:  Expert Opin Pharmacother       Date:  2001-07       Impact factor: 3.889

3.  Isolation and analysis of immune complexes from sera of patients with polymyalgia rheumatica and giant cell arteritis.

Authors:  A J Smith; V Kyle; T E Cawston; B L Hazleman
Journal:  Ann Rheum Dis       Date:  1987-06       Impact factor: 19.103

4.  An elderly lady with a painful swollen face.

Authors:  Kristel Van Landuyt; Steven Vanderschueren
Journal:  Eur J Intern Med       Date:  2007-11-26       Impact factor: 4.487

Review 5.  Hereditary angioedema in childhood: an approach to management.

Authors:  Didier G Ebo; Marjoke M Verweij; Kathleen J De Knop; Margo M Hagendorens; Chris H Bridts; Luc S De Clerck; Wim J Stevens
Journal:  Paediatr Drugs       Date:  2010-08-01       Impact factor: 3.022

6.  First case of acquired functional C1(-) INH deficiency: association with angioedema during Churg and Strauss vasculitis.

Authors:  J L Pasquali; D Christmann; F Modert; P C Belval; D Storck; G Hauptmann
Journal:  Int Arch Allergy Appl Immunol       Date:  1984

7.  Hereditary angioedema presenting in late middle age after angiotensin-converting enzyme inhibitor treatment.

Authors:  Anthony J Ricketti; Dennis J Cleri; Luz S Ramos-Bonner; John R Vernaleo
Journal:  Ann Allergy Asthma Immunol       Date:  2007-04       Impact factor: 6.347

8.  Facial swelling and giant cell arteritis.

Authors:  M D Cohen; W W Ginsburg; G L Allen
Journal:  J Rheumatol       Date:  1982 Mar-Apr       Impact factor: 4.666

9.  Serum levels of immunoglobulin and complement in giant-cell arteritis.

Authors:  B E Malmvall; B A Bengtsson; B Kaijser; L A Nilsson; K Alestig
Journal:  JAMA       Date:  1976-10-18       Impact factor: 56.272

10.  Acquired angioedema associated with hereditary angioedema due to C1 inhibitor deficiency.

Authors:  M Guilarte; O Luengo; C Nogueiras; M Labrador-Horrillo; E Muñoz; A López; V Cardona
Journal:  J Investig Allergol Clin Immunol       Date:  2008       Impact factor: 4.333

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