Central nervous involvement, mainly with symptoms of cranial neuropathies, occurs in 2–8% of patients with granulomatosis with polyangiitis (GPA). Meningeal involvement, with persistent and severe headache as main manifestation and abnormal thickening and enhancement of the dural mater on postcontrast magnetic resonance imaging, is extremely rare. We present a case of pachymeningitis due to limited GPA, providing simultaneously a literature review
Background. Hypertrophic pachymeningitis (HP) is generally regarded as a rare inflammatory disease, ...
tures of the case of a 41-year-old man with Wegener granulo-matosis presenting with neurologic sympt...
Idiopathic hypertrophic pachymeningitis is a rare form of granulomatous meningitis. It is mainly a d...
Central nervous system (CNS) involvement, such as pachymeningitis and/or cerebrovascular events, is ...
ABSTRACT This report aims to show an unusual case of granulomatosis with polyangeitis (GPA), previou...
Abstract Background Granulomatosis with polyangiitis ...
The purpose of this case-based review is to highlight cranial nerve involvement in granulomatosis wi...
Granulomatosis with Poliangeitis or Wegner's granulomatosis has an incidence of5-10 cases per millio...
Wegener’s granulomatosis or granulomatosis polyangiitis associated (GPA) is a granulomatous inflamma...
The purpose of this case-based review is to highlight cranial nerve involvement in granulomatosis wi...
A 75-year-old woman presented with rapidly progressive glomerulonephritis with positive results for ...
Inrtoduction: Granulomatosis with polyangiitis (GPA) is a systematic and necrotizing vasculitis with...
Hypertrophic pachymeningitis is a rare inflammatory condition that leads to the thickening of the du...
Background: Granulomatosis with polyangiitis (formerly Wegener's granulomatosis) is a multisystem va...
Granulomatosis with polyangiitis (GPA) is an antineutrophil cytoplasmic antibody-associated granulom...
Background. Hypertrophic pachymeningitis (HP) is generally regarded as a rare inflammatory disease, ...
tures of the case of a 41-year-old man with Wegener granulo-matosis presenting with neurologic sympt...
Idiopathic hypertrophic pachymeningitis is a rare form of granulomatous meningitis. It is mainly a d...
Central nervous system (CNS) involvement, such as pachymeningitis and/or cerebrovascular events, is ...
ABSTRACT This report aims to show an unusual case of granulomatosis with polyangeitis (GPA), previou...
Abstract Background Granulomatosis with polyangiitis ...
The purpose of this case-based review is to highlight cranial nerve involvement in granulomatosis wi...
Granulomatosis with Poliangeitis or Wegner's granulomatosis has an incidence of5-10 cases per millio...
Wegener’s granulomatosis or granulomatosis polyangiitis associated (GPA) is a granulomatous inflamma...
The purpose of this case-based review is to highlight cranial nerve involvement in granulomatosis wi...
A 75-year-old woman presented with rapidly progressive glomerulonephritis with positive results for ...
Inrtoduction: Granulomatosis with polyangiitis (GPA) is a systematic and necrotizing vasculitis with...
Hypertrophic pachymeningitis is a rare inflammatory condition that leads to the thickening of the du...
Background: Granulomatosis with polyangiitis (formerly Wegener's granulomatosis) is a multisystem va...
Granulomatosis with polyangiitis (GPA) is an antineutrophil cytoplasmic antibody-associated granulom...
Background. Hypertrophic pachymeningitis (HP) is generally regarded as a rare inflammatory disease, ...
tures of the case of a 41-year-old man with Wegener granulo-matosis presenting with neurologic sympt...
Idiopathic hypertrophic pachymeningitis is a rare form of granulomatous meningitis. It is mainly a d...