Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Cytoplasmic antineutrophil cytoplasmic antibody"'
Publikováno v:
Clinical Pulmonary Medicine. 26:63-67
The pulmonary vasculitides include a wide spectrum of disorders that have in common inflammation and destruction of pulmonary blood vessels. Granulomatosis with polyangiitis (GPA), formerly known as Wegener granulomatosis, is the most common of the a
Autor:
Javier Pereira Beceiro, Teresa Mosquera Seoane, Carlos Bonelli Martín, Miguel A. Cuerpo Pérez, Javier Pérez Valcárcel, Andrés Rodríguez Alonso
Publikováno v:
Reumatología Clínica (English Edition). 10:409-412
Objectives: We present a case of prostatitis with acute urinary retention as a rare initial manifestation of Wegener’s granulomatosis. Methods: The case was a 48-year-old male with symptoms of prostatitis over 10 days. The patient presented urinary
Publikováno v:
Anales de Pediatría, Vol 79, Iss 6, Pp 381-384 (2013)
Resumen: La granulomatosis de Wegener pertenece al grupo de vasculitis de vaso pequeño asociadas a anticuerpos anticitoplasma de neutrófilo. Se caracteriza por inflamación granulomatosa y vasculitis necrosante que puede afectar a diversos órganos
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Autor:
Basile Nicolas Landis, Piero Ballinari, Peter M. Villiger, Marco Caversaccio, Yara Banz, Patrick Dubach, Urs Borner
Publikováno v:
American Journal of Rhinology and Allergy, Vol. 26, No 6 (2012) pp. 475-80
Background A substantial proportion of Wegener's disease (WG) patients present with localized disease of the upper airways, i.e., sinonasal and other ear/nose/throat (ENT) symptoms. Because of the oligosymptomatic presentation a timely diagnosis of t
Autor:
Ihsaan Al-hadad, Omar Taha
Publikováno v:
Respiratory Medicine CME. 3(3):192-194
A 34-year-old male was admitted to hospital for the suspicion of pulmonary tuberculosis. He underwent haematological investigations and radiological tests which were compatible with this diagnosis. However, the lack of microbiological confirmation to
Publikováno v:
Journal of clinical rheumatology : practical reports on rheumaticmusculoskeletal diseases. 15(5)
Publikováno v:
Auris, nasus, larynx.
(1) Objective: Currently Wegener's granulomatosis (WG) is diagnosed from clinical features, a test for antineutrophil cytoplasmic antibody (ANCA) and histological confirmation. The purpose of our study was to evaluate histological findings, in partic
Publikováno v:
The Journal of Association of Chest Physicians, Vol 2, Iss 2, Pp 75-77 (2014)
Pulmonary involvement in Wegener′s granulomatosis (WG) usually starts with nonspecific symptoms such as cough, dyspnea, hemoptysis, and pleuritis. Spontaneous pneumothorax as initial presentation is extremely rare. Although its real incidence is un
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