SciELO - Scientific Electronic Library Online

 
vol.15 issue5COPD exacerbation or something else: Clinical caseSpontaneous hemothorax in a neurofibromatosis type I patient: A case report author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

  • Have no similar articlesSimilars in SciELO

Share


Revista Portuguesa de Pneumologia

Print version ISSN 0873-2159

Abstract

FIGUEIREDO, Sandra et al. Wegener granulomatosis: Otologic, nasal, tracheobronchial and pulmonary involvement. Rev Port Pneumol [online]. 2009, vol.15, n.5, pp.929-935. ISSN 0873-2159.

Wegener granulomatosis is a rare systemic idiopathic disease characterized by involvement of small vessels - medium and small arteries, venules, arterioles and ocasionally large arteries. This disease has predilection for the upper and lower respiratory tract and the kidney, with granulomatous inflamation and necrosis. Clinical manifestations and organ involvement of the disease vary widely. Early diagnosis and treatment may lead to a full recovery. Without treatment, Wegener’s granulomatosis can be fatal. The authors present a case of a 33 year-old female, with severe disease, but with good outcome, after adequate diagnosis and treatment.

Keywords : Wegener´s granulomatosis; severe limited form.

        · abstract in Portuguese     · text in Portuguese     · Portuguese ( pdf )