Literature DB >> 7205833

Wegener's granulomatosis and relapsing polychondritis: a case report.

P Small, M Black, M Davidman, M L de Champlain, M A Kapusta, H Kreisman.   

Abstract

Relapsing polychondritis, a rare disorder characterized by inflammation of cartilaginous tissue, is often associated with vasculitic features. Wegener's granulomatosis is an uncommon form of vasculitis, usually responsive to treatment with cyclophosphamide. A 59-yr-old man with relapsing polychondritis, initially well controlled by corticosteroid therapy, developed pulmonary infiltrates and glomerulonephritis. After pathological confirmation of Wegener's granulomatosis, cyclophosphamide therapy was instituted and remission achieved.

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Year:  1980        PMID: 7205833

Source DB:  PubMed          Journal:  J Rheumatol        ISSN: 0315-162X            Impact factor:   4.666


  6 in total

1.  Erosive arthritis in relapsing polychondritis.

Authors:  A S Jawad; M Burrel; K L Lim; D G Scott
Journal:  Postgrad Med J       Date:  1990-09       Impact factor: 2.401

2.  Saddle-nose and bilateral cauliflower ear deformities with pyoderma gangrenosum-like ulcers, cavitary pulmonary lesions, digital gangrene and pulselessness in a young female.

Authors:  Sweta Subhadarshani; Vishal Gupta; Anurag Chahal; Kaushal K Verma
Journal:  BMJ Case Rep       Date:  2017-06-15

3.  Relapsing polychondritis as a secondary phenomenon of primary systemic vasculitis.

Authors:  K Handrock; W L Gross
Journal:  Ann Rheum Dis       Date:  1993-12       Impact factor: 19.103

4.  Salivary gland involvement as initial presentation of Wegener's disease.

Authors:  B G Vanhauwaert; T A Roskams; S B Vanneste; D C Knockaert
Journal:  Postgrad Med J       Date:  1993-08       Impact factor: 2.401

5.  Relapsing polychondritis with p-ANCA associated vasculitis: Which triggers the other?

Authors:  Ibolya File; Csilla Trinn; Zsolt Mátyus; László Ujhelyi; József Balla; János Mátyus
Journal:  World J Clin Cases       Date:  2014-12-16       Impact factor: 1.337

6.  Relapsing polychondritis presenting as cutaneous polyarteritis nodosa.

Authors:  G Rauh; I Kamilli; U Gresser; M Landthaler
Journal:  Clin Investig       Date:  1993-04
  6 in total

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