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Hypertrophic pachymeningitis in a patient with ANCA negative granulomatosis with polyangiitis: A case report / Paquimeningitis hipertrófica en un paciente con granulomatosis con poliangeítis ANCA negativo: reporte de un caso
Huaringa-Marcelo, Jorge; Tapia-Orihuela, Rubén Kevin Arnold; Loja-Oropeza, David.
  • Huaringa-Marcelo, Jorge; Universidad Científica del Sur. Facultad de Ciencias de la Salud. Lima. PE
  • Tapia-Orihuela, Rubén Kevin Arnold; Universidad Nacional Mayor de San Marcos. Facultad de Medicina de San Fernando. Lima. PE
  • Loja-Oropeza, David; Hospital Nacional Arzobispo Loayza. Lima. PE
Rev. colomb. reumatol ; 27(4): 291-297, oct.-dic. 2020. tab, graf
Article in English | LILACS | ID: biblio-1289333
ABSTRACT
ABSTRACT Granulomatosis with polyangiitis (GPA) is a vasculitic disease with an infrequent involvement of the central nervous system. This can lead, in rare cases, to hypertrophic pachymeningitis (HP), which is characterized by inflammation and fibrosis that cause a thickening of dura mater. At present, it is crucial to consider GPA in the differential diagnosis of elderly patients with intracranial hypertension. The case is presented of a 60-year-old male with progressive severe headache, vomiting, and wasting syndrome. Physical examination showed pallor, weight loss, and unilateral papilloedema. A gadolinium-enhanced brain MRI scan showed sinusitis, chronic otomastoiditis, and hypertrophic pachymeningitis. Finally, a meningeal biopsy concluded a necrotising granulomatous vasculitis compatible with GPA. However, PR3- and MPO-ANCA were negative. After corticosteroid therapy was initiated, the patient had a favorable outcome during his hospital stay.
RESUMEN
RESUMEN La granulomatosis con poliangeítis (GPA) compromete excepcionalmente el sistema nervioso central, conllevando en raras ocasiones a una paquimeningitis hipertrófica (PH), caracterizada por inflamación y fibrosis, que originan un engrosamiento de la duramadre. Actualmente, su consideración es crucial en el diagnóstico diferencial de pacientes ancianos con hipertensión endocraneana. Presentamos el caso de un adulto de 60 anos con cefalea severa progresiva, vómitos, papiledema unilateral y síndrome consuntivo en donde la resonancia magnética cerebral contrastada con gadolinio muestra sinusitis, otomastoiditis y PH. Finalmente, la biopsia de meninges reveló vasculitis granulomatosa necrosante de pequenos y medianos vasos compatible con GPA. Empero, PR3- y MPO-ANCA resultaron negativos. Se inició terapia con corticoides, presentando una evolución clínica favorable durante su hospitalización.
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Full text: Available Index: LILACS (Americas) Main subject: Granulomatosis with Polyangiitis / Meningitis Type of study: Diagnostic study Limits: Humans / Male Language: English Journal: Rev. colomb. reumatol Journal subject: Rheumatology Year: 2020 Type: Article Affiliation country: Peru Institution/Affiliation country: Hospital Nacional Arzobispo Loayza/PE / Universidad Científica del Sur/PE / Universidad Nacional Mayor de San Marcos/PE

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Full text: Available Index: LILACS (Americas) Main subject: Granulomatosis with Polyangiitis / Meningitis Type of study: Diagnostic study Limits: Humans / Male Language: English Journal: Rev. colomb. reumatol Journal subject: Rheumatology Year: 2020 Type: Article Affiliation country: Peru Institution/Affiliation country: Hospital Nacional Arzobispo Loayza/PE / Universidad Científica del Sur/PE / Universidad Nacional Mayor de San Marcos/PE