Results 51 to 60 of about 5,850 (214)

Acute Wegener's granulomatosis [PDF]

Thorax, 1967
Two cases of acute Wegener's granulomatosis are described. The first ended fatally after an illness of only two weeks. In the second a remission of three years has been obtained with heavy doses of steroid. At present there is evidence of impaired pulmonary gas transfer and also chronic glomerulonephritis, but the patient is asymptomatic.
D, Leak, G P, Clein
openaire   +2 more sources

Paresthesia and Facial Bone Destruction due to Chronic Granulomatous Invasive Aspergillosis in the Left Maxillary Sinus

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT We report a case of chronic granulomatous invasive aspergillosis in a 56‐year‐old male teacher from South Kordofan, Sudan, who underwent surgery in 2007 to remove his left orbital aspergillus granuloma. The patient developed progressive facial swelling beginning in 2017 and paraesthesia in the left zygomatico‐maxillary region, despite initial ...
Rawa Badri, Matthew C. Fisher, Ahmed Hassan Fahal   +2 more
wiley   +1 more source

Cytomegalovirus retinitis presenting as vasculitis in a patient with Wegener’s granulomatosis

Clinical Ophthalmology, 2008
Paris G Tranos1, Ilias Georgalas2, Panagiota Founti1, Ioannis Ladas21Papageorgiou University Hospital, Thessaloniki, Greece; 2Department of Ophthalmology, “G.Genimatas” Hospital, Athens, GreecePurpose: To present an unusual case of ...
Paris G Tranos, Ilias Georgalas, Panagiota Founti, Ioannis Ladas   +3 more
doaj  

Granulomatosis de Wegener y Abordaje Enfermero [PDF]

, 2015
Este trabajo de fin de grado se basa en una revisión bibliográfica de toda la información que hay, hoy en día, sobre la granulomatosis de Wegener y en la unificación de criterios de actuación para la elaboración de un plan de cuidados de enfermería ...
Marcos Flores, Marta
core  

On the Wegener granulomatosis associated region on chromosome 6p21.3 [PDF]

, 2006
Background Wegener granulomatosis (WG) belongs to the heterogeneous group of systemic vasculitides. The multifactorial pathophysiology of WG is supposedly caused by yet unknown environmental influence(s) on the basis of genetic predisposition.
Paweł Szyld, Peter Jagiello, Elena Csernok, Wolfgang L Gross, Joerg T Epplen, CO Savage, RA Watts, JC Jennette, RJ Falk, RA Watts, B Miterski, B Hellmich, J Ludemann, U Specks, YM van der Geld, VL Esnault, M Gencik, D Huang, S Meller, S Borgmann, SJ Spencer, MF Cotch, EC Hagen, ME Griffith, P Jagiello, CV Jongeneel, AJ Jeffreys, R Valentonyte, VC Yu, C Mathieu, L Adorini, L Adorini, L Adorini, RY Leavitt, JD Storey, Storey, H Ishiguro, S Wieczorek, P Katz, KB Elkon, SS Papiha, M Gencik, R Rajsbaum, P Jagiello, H Ueda, LA Criswell   +45 more
core   +2 more sources

Demographic and Clinical Insights Into Pyoderma Gangrenosum: A Retrospective Cross‐Sectional Study From a Tertiary Care Hospital

Health Science Reports, Volume 9, Issue 4, April 2026.
ABSTRACT Background and Aims Pyoderma gangrenosum (PG) is a rare, non‐infectious inflammatory skin disease often associated with systemic disorders such as inflammatory bowel disease (IBD), malignancies, and autoimmune conditions. This study aimed to investigate the demographic characteristics, comorbidities, differential diagnoses, and treatment ...
Mitra Mirzaei, Alireza Jafarzadeh, Sepideh Salehi, Azadeh Goodarzi   +3 more
wiley   +1 more source

Cranial Nerve Injury as an Initial Sign of Wegener Granulomatosis: Misdiagnosis and Fatal Course in Two Cases

Turkish Journal of Nephrology, 2019
Highest prevalence of all antineutrophil cytoplasmic antibody associated systemic vasculitides is the Wegener granulomatosis, and it’s typically characterized by a necrotizing granulomatous vasculitis of the respiratory tracts, kidneys, and skin ...
Kenan TURGUTALP, Engin KARA, Mehmet HOROZ, Ebru YILMAZ, Ebru GÖK OĞUZ, Sezer ÇİÇEKLİ TURGUTALP, İclal GÜRSES, Feray TABAKAN, Tolga KÖŞECİ, Ahmet KIYKIM   +9 more
doaj  

Immunosuppression and Surgery‐Free Interval in Granulomatosis With Polyangiitis Airway Stenosis

The Laryngoscope, Volume 136, Issue 4, Page 1858-1865, April 2026.
Subglottic and tracheal stenosis are severe manifestations of granulomatosis with polyangiitis (GPA) that often require both endoscopic intervention and systemic immunosuppression. Rituximab may help stabilize GPA‐related airway disease by prolonging the interval between endoscopic procedures and delaying relapse.
Sydney J. Torres, Andrew J. Neevel, Julia A. Ford, Lawrence Kashat, Norman D. Hogikyan, Robbi A. Kupfer, Robert J. Morrison   +6 more
wiley   +1 more source

Granulomatosis with Polyangiitis (Wegener Granulomatosis) Mimicking Infective Endocarditis

European Journal of Case Reports in Internal Medicine, 2014
Introduction Infective endocarditis (IE) has been reported to mimic granulomatosis with polyangiitis (GPA) and to test positive to antineutrophil cytoplasmic antibodies (ANCA), which may lead to a misdiagnosis and inappropriate treatment.
Imène Rachdi, Lilia Baili, Fatma Daoud, Zohra Aydi, Hana Zoubeidi, Basma Ben Dhaou, Fatma Boussema   +6 more
doaj   +1 more source

Onset of granulomatosis with polyangiitis obscured by heart disease in an elderly man

Radiology Case Reports, 2020
We describe a case of 85-year-old man who presented to the Emergency Department with sudden dyspnea. He had a past medical history of cardiomyopathy and radiography and nonenhanced computed tomography (CT) of the chest showed pulmonary edema.
C. Pace, M. Presicce, F. Lamacchia, D. Ferrari, G. Sergiacomi   +4 more
doaj   +1 more source