A Wegener granulomatózis és a gyulladásos miopátiák tüdőmanifesztációjának klinikai megjelenésével és ezek kialakulásához vezető immunológiai eltérésekkel kapcsolatos vizsgálatok [PDF]
, 2004 6
Komócsi András
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Immunity, Inflammation and Disease, Volume 14, Issue 3, March 2026.Autoimmune disorder patients are vulnerable to cytomegalovirus (CMV) infections, which can present with symptoms that mimic flare‐ups of the underlying disease. We present two cases: a 44‐year‐old woman with systemic lupus erythematosus and a 55‐year‐old man with sarcoidosis, both of whom developed unusual manifestations linked to CMV infection ...
Elaheh Karimi +5 more
wiley +1 more source
Научно-практическая ревматология, 2012 The author studied in detail the specific features of the clinical manifestations reflecting a granulomatous inflammatory response and necrotizing polyangiitis, by using her experience in following up 70 patients with granulomatosis and polyangiitis ...
Tatiana Valentinovna Beketova
doaj +1 more source
Chemosensory function in Wegener's granulomatosis: a preliminary report [PDF]
, 2018 Despite the fact that Wegener's granulomatosis affects the nasal and paranasal cavities and the cranial nerves regularly, chemosensory impairments have not been reported.
Cao Van, Helene +4 more
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Clinical insights on Tolosa Hunt syndrome: a multidisciplinary approach on neurological-related symptomatology in maxillofacial region [PDF]
, 2018 Background Tolosa–Hunt syndrome (THS) related neurological symptoms are described in literature as “unilateral”, “recurrent”, “episodic”, “intense”, “severe”, “lancinating” or “stabbing” pain on the upper face and forehead and may be misdiagnosed ...
Ahmed Siddiqui, Ammar +8 more
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The Drug Safety Framework of Avacopan: A Pharmacovigilance Study
Medicine Advances, Volume 4, Issue 1, Page 77-89, March 2026.We identified 11 previously unreported potential adverse events associated with avacopan. No high‐priority clinical events were observed; however, special attention should be paid to the potential possibility of avacopan‐induced vanishing bile duct syndrome (Logos and icons displayed in the sections “Safety Framework” and “Data Sources and ...
Tianqi Chang +4 more
wiley +1 more source
ELEVATED SERUM LEVELS OF TNF SOLUBLE RECEPTORS IN PATIENTS WITH POSITIVE ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODIES [PDF]
, 2017 ANCA are found in various systemic vasculitis and are supposed to play a role in the pathogenesis of the disease, in cooperation with other factors such as cytokines.
DAYER, J.-M +3 more
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Clinical and Pathological Features of Vasculitic Neuropathy: A Single‐Center Study in China
European Journal of Neurology, Volume 33, Issue 3, March 2026.Vasculitic neuropathy in mainland China predominantly presents as axonal sensorimotor neuropathy. Systemic VN shows more frequent transmural inflammatory infiltration, whereas EGPA is more common in cases without infiltration. Most treated patients achieved remission, and the overall prognosis was relatively favorable, underscoring the importance of ...
Xiaoyu Zhou +9 more
wiley +1 more source
Limited granulomatosis with polyangiitis presenting as an isolated lung lesion
Indian Journal of Pathology and Microbiology, 2020 Granulomatosis with polyangiitis (GPA) is a systemic necrotizing vasculitis involving small and medium-sized blood vessels and granulomatous inflammation of upper and lower respiratory systems and/or renal system.
Shameera Begum +3 more
doaj +1 more source
Vasculitides associated with IgG antineutrophil cytoplasmic autoantibodies in childhood [PDF]
, 2018 Immunoglobulin (Ig)G antineutrophil cytoplasmic autoantibodies are causally associated with necrotizing vasculitides that are characterized immunopathologically by little or no deposition of immunoreactants, such as Wegener granulomatosis, microscopic ...
Bettinelli, Alberto +4 more
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