Literature DB >> 19508947

Vasculitis of the upper and lower airway.

M Martinez Del Pero1, P Sivasothy.   

Abstract

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.

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Year:  2009        PMID: 19508947     DOI: 10.1016/j.berh.2009.02.003

Source DB:  PubMed          Journal:  Best Pract Res Clin Rheumatol        ISSN: 1521-6942            Impact factor:   4.098


  5 in total

1.  Granulomatosis with polyangiitis causing subglottic stenosis-two cases and their management.

Authors:  Victoria Blackabey; Richard Wei Chern Gan; Helen Buglass; Veena Kaul; Victoria M M Ward
Journal:  AME Case Rep       Date:  2018-04-30

2.  Rhinologic and sinonasal changes in PR3 ANCA pulmonary vasculitis.

Authors:  Katarzyna Zycinska; K A Wardyn; E Piotrowska; T M Zielonka; H Zycinski; A Bogaczewicz; A Nitsch-Osuch; M Miskiewicz; R Smolarczyk
Journal:  Eur J Med Res       Date:  2010-11-04       Impact factor: 2.175

Review 3.  Proteinase 3-ANCA Vasculitis versus Myeloperoxidase-ANCA Vasculitis.

Authors:  Marc Hilhorst; Pieter van Paassen; Jan Willem Cohen Tervaert
Journal:  J Am Soc Nephrol       Date:  2015-05-08       Impact factor: 10.121

4.  ANCA-negative Wegener's granulomatosis with multiple lower cranial nerve palsies.

Authors:  Sung-Hee Kim; Jin Park; Jung Ho Bae; Min-Sun Cho; Kee Duk Park; Jee Hyang Jeong
Journal:  J Korean Med Sci       Date:  2013-10-31       Impact factor: 2.153

5.  Upper respiratory system involvement as the only manifestation of granulomatosis with polyangiitis in a child with marfan phenotype.

Authors:  Reza Amin; Soheila Alyasin; Tooba Momen; Maryam Khoshkhouy; Sepideh Darougar
Journal:  Tanaffos       Date:  2013
  5 in total

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