Wegener's granulomatosis presenting with otologic and neurologic symptoms: clinical and pathological correlations.

J Oral Pathol Med

Departement of Otorhinolaryngology, Torino Nord Emergenza, Ospedale San Giovanni Bosco, Piazza Donatori del Sangue, Torino, Italy.

Published: August 2003

A case of Wegener's granulomatosis in a 59-year-old woman is reported. The disease first involved the parotid gland, the brain stem and the spinal cord, then running a rapidly progressive course as systemic pathology. Anti-neutrophil cytoplasmic antibody (cANCA) levels raised as renal failure set in. Renal biopsy confirmed the diagnosis of Wegener's granulomatosis and an appropriate therapy was adopted.

Download full-text PDF

Source
http://dx.doi.org/10.1034/j.1600-0714.2003.t01-1-00152.xDOI Listing

Publication Analysis

Top Keywords

wegener's granulomatosis
12
granulomatosis presenting
4
presenting otologic
4
otologic neurologic
4
neurologic symptoms
4
symptoms clinical
4
clinical pathological
4
pathological correlations
4
correlations case
4
case wegener's
4

Similar Publications

Objective: To investigate the similarities and differences of clinical manifestations and long-term prognosis between eosinophilic gastroenteritis (EGE) and eosinophilic granulomatosis with polyangiitis (EGPA) complicating GI involvement (EGPA-GI).

Methods: Sixty-two EGE and 30 EGPA-GI patients were retrospectively enrolled in PUMCH from 2008 to 2023. Baseline clinical records were collected.

View Article and Find Full Text PDF

Background: Glucocorticoids are central to vasculitis treatment but increase vertebral fracture risk. This study assessed whether vasculitis as the cause of ESRD is associated with incident vertebral fracture, controlling for corticosteroid use.

Methods: A retrospective cohort study was conducted from 2006-2019 on adults in the U.

View Article and Find Full Text PDF

Granulomatosis with polyangiitis (GPA) is a small-to-medium vessel vasculitis that can affect the skin, respiratory tract, kidneys and other organs. A rare cutaneous manifestation of GPA is pyoderma gangrenosum (PG)-like ulcerations, which can have debilitating and disfiguring consequences. We report the case of a man in his 40s with refractory PG-like ulcerations secondary to GPA, not responsive to conventional immunosuppression, who was successfully treated with rituximab.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!