Results 31 to 40 of about 13,581 (183)

Intestinal involvement in Wegener's granulomatosis

, 2007
Wegener's granulomatosis is a necrotizing vasculitis that may affect any viscera. Gastrointestinal involvement is rather uncommon. We present a case of Wegener's granulomatosis with multiple small bowel ulcers and a single ileal perforation. Histological
Soekmensueer, Cenk, DENİZ, KEMAL, Oezseker, Havva S., BALAS, ŞENER, Akpynar, Erhan   +4 more
core   +2 more sources

Wegener's Granulomatosis presenting with an abscess in the parotid gland: a case report

Journal of Medical Case Reports, 2009
Introduction Wegener's Granulomatosis is a vasculitis of uncertain aetiology. Affected patients usually present with disease of the respiratory and renal tracts.
Geyer Marcel, Kulamarva Gautham, Davis Anne   +2 more
doaj   +1 more source

Wegener's granulomatosis presenting as pyoderma gangrenosum

, 2007
Half of the patients with Wegener's granulomatosis develop skin lesions due to the systemic vasculitis. Wegener's granulomatosis should be included in the differential diagnostic considerations for necrotic ulcers, including leg ulcers. We present a case
Nievergelt, Helga, Braathen, Lasse R, Clara Boudny, Lasse R. Braathen, Boudny, Clara, Dagmar Simon, Helga Nievergelt, Simon, Dagmar   +7 more
core   +1 more source

Wegener’s granulomatosis in a middle-aged woman presenting with dyspnea, rash, hemoptysis and recurrent eye complaints: a case report

Journal of Medical Case Reports, 2012
Introduction Wegener’s granulomatosis presenting as diffuse alveolar hemorrhage is uncommon. However, the recognition of multisystem disease involving joints, kidney, eye and lung is critical for diagnosing Wegener's vasculitis.
Cardenas-Garcia Jose, Farmakiotis Dimitrios, Baldovino Berta-Paola, Kim Peter   +3 more
doaj   +1 more source

An unusual case of granulomatosis with polyangiitis with unilateral parotid gland enlargement

Clinical Case Reports, 2023
Key Clinical Message Here, we report a case of granulomatosis with polyangiitis presenting with unilateral parotid gland enlargement and later developed skin lesions on the lower extremities and abdomen.
Toktam Safari Giv, Ghazal Mardani, Azadeh Rakhshan, Mohammad Kouhestany, Hamideh Moravvej   +4 more
doaj   +1 more source

An Unusual Presentation of Granulomatosis with Polyangiitis [PDF]

Journal of Cardio-Thoracic Medicine, 2017
The granulomatosis with polyangiitis (GPA), formerly known as Wegener’s granulomatosis, is a pauci-immune vasculitis involving small- and medium-sized blood vessels.
Rakhee Sodhi, Sushant Khanduri, Varuna Jethani, Shirazi Nadia, Manoj Kumar   +4 more
doaj   +1 more source

Wegener's granulomatosis presenting as meningitis

, 2011
Background:Wegener's granulomatosis is a rare but well recognised autoimmune necrotising vasculitis. Presentation of disease in the head and neck is common and mostly consists of nasal crusting, blockage and bloody discharge. Neurological presentation is
G Thiel, M Shakeel, K Ah-See
core   +1 more source

Hepatic involvement in Wegener's granulomatosis: a case report

Journal of Medical Case Reports, 2010
Introduction We report the case of a 58-year-old Caucasian Greek man who presented with dry cough, fever, bilateral alveolar infiltrates and acute hepatitis.
Trigidou Rodoula, Paissios Nicolas P, Goritsas Constantin, Delladetsima Joanna   +3 more
doaj   +1 more source

Wegener's Granulomatosis (Granulomatosis with Polyangiitis). Difficulties in Diagnosis in the Post-COVID Period

Туберкулез и болезни лёгких, 2023
The article describes a clinical case of Wegener's granulomatosis, which manifested in the post-COVID period in a young man; also it discusses diagnostic difficulties.
B. E. Borodulin, E. A. Borodulina, S. Yu. Pushkin, E. S. Vdoushkina, L. V. Povalyaeva   +4 more
doaj   +1 more source

Biosimilar Rituximab in ANCA‐Associated Vasculitis Compared to the Originator: A Multicenter Cohort Study

ACR Open Rheumatology, Volume 8, Issue 8, August 2026.
Objective To evaluate the six‐month effectiveness and safety of rituximab biosimilars compared to the originator in granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA), and outcomes following originator to biosimilar switching. Methods We recruited adults with GPA or MPA treated with the rituximab originator or a biosimilar for ...
Arielle Mendel, Lillian Barra, Hassan Behlouli, Sasha Bernatsky, Alison H. Clifford, Jan Willem Cohen Tervaert, Natasha Dehghan, Aurore Fifi‐Mah, Jean‐Paul Makhzoum, Rosalie‐Sélène Meunier, Nataliya Milman, Medha Soowamber, Elaine Yacyshyn, Nader Khalidi, Christian Pagnoux   +14 more
wiley   +1 more source