Best Practice & Research Clinical Rheumatology
Volume 23, Issue 3 , Pages 403-417, June 2009

Vasculitis of the upper and lower airway

  • M. Martinez Del Pero, MRCS

      Affiliations

    • Department of ENT, Addenbrooke's Hospital, Cambridge, UK
  • ,
  • P. Sivasothy, MD

      Affiliations

    • Department of Respiratory Medicine, Addenbrooke's Hospital, Cambridge, UK
    • Corresponding Author InformationCorresponding author. Dr. P. Sivasothy, Department of Respiratory Medicine, Addenbrooke's Hospital, Cambridge, CB2 2QQ, UK. Tel.: +44 1223 245151x2646; Fax: +44 1223.

The pulmonary vasculitides are a heterogeneous group of rare disorders that result from an inflammatory process damaging the vessel wall and consequent impaired blood flow, ischaemia and tissue necrosis. The clinical manifestation of these vasculitides depends on the site, size, type and severity of the inflammatory process.

Vasculitis involving the airways is a common feature of the anti-neutrophil cytoplasmic antibody (ANCA)-associated systemic vasculitides (AASVs) and can predate the diagnosis by years. Secondary causes of vasculitis associated with connective tissue disorders are also capable of presenting with pulmonary features. Recognition of involvement, investigation and treatment are important to ameliorate symptoms for patients. This article concentrates on the assessment and specific management of upper and lower airway problems of AASV.

Keywords: Wegener's granulomatosis, microscopic polyangittis, Churg–Strauss syndrome, upper airway, airway stenosis, asthma

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PII: S1521-6942(09)00024-2

doi:10.1016/j.berh.2009.02.003

Best Practice & Research Clinical Rheumatology
Volume 23, Issue 3 , Pages 403-417, June 2009