Results 51 to 60 of about 45,538 (193)
Objective The objective of the study was to determine risk factors for relapse of antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis (AAV) after reinduction of remission with rituximab and discontinuation of maintenance therapy. Methods This is a post hoc analysis of the RITAZAREM clinical trial.
Ellen Romich +62 more
wiley +1 more source
Severe Wegener's granulomatosis successfully treated with rituximab
The paper discusses the problems of the diagnosis and treatment of Wegener's granulomatosis, the most common anti-neutrophil cytoplasmic antibody-associated systemic vasculitis.
E N Semenkova +7 more
doaj
The article presents a clinical case that confirms the importance of careful collection and analysis of medical history and active identification of pathology of the upper respiratory tract, middle ear and eyes typical of the debut of Wegener's ...
M. D. Romanov, T. M. Levina
doaj +1 more source
Wegener's Granulomatosis Presenting With an Isolated Paranasal Sinus Involvement in a Child
Wegener's granulomatosis which is rarely seen in children is an idiopathic necrotizing granulomatous vasculitis, affecting primarily paranasal sinuses, nasopharynx, lungs, kidneys and joints. In this article, we report a very rare case of eight-year-old
Ghaniya DAAR +5 more
doaj
ABSTRACT Lateral medullary syndrome (LMS) or Wallenberg's syndrome is usually caused by a cerebrovascular accident of the vertebral artery or the posterior inferior cerebellar artery (PICA), leading to damage to the dorsolateral aspects of the medulla oblongata.
Abera Kuma +5 more
wiley +1 more source
Granulomatosis with polyangitis (Wegener's) [PDF]
A 51-year-old woman was admitted to our hospital with general fatigue, fever and cough. Upon examination, sinusitis, papules of the planta, polymorph leucocytosis, hypoalbuminaemia and an elevated level of PR3-antineutrophil cytoplasmic antibodies (ANCAs) were found.
Takayuki, Takimoto +4 more
openaire +2 more sources
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 +2 more
wiley +1 more source
Clinical features of childhood granulomatosis with polyangiitis (wegener’s granulomatosis)
BackgroundGranulomatosis with polyangiitis (GPA), formerly known as Wegener’s granulomatosis (WG), belongs to the group of ANCA-associated necrotizing vasculitides.
M. Bohm +27 more
semanticscholar +1 more source
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 +3 more
wiley +1 more source
Subglottic stenosis is one of the major complications of the Wegener’s granulomatosis. There are no set guidelines available for management. Intralesional steroid injection and dilatation seems to be a safe and successful method of treatment. We report a
Jawaid Naeem Qureshi
doaj

