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Rev. bras. oftalmol ; 77(4): 203-206, jul.-ago. 2018. tab, graf
Article in Portuguese | LILACS | ID: biblio-959095

ABSTRACT

RESUMO O presente relato tem o objetivo de mostrar um caso incomum de Granulomatose com Poliangeíte (GPA), que previamente era denominada Granulomatose de Wegener. Trata-se de é uma doença multissistêmica, caracterizada por inflamação granulomatosa necrotizante e vasculite que envolve principalmente o trato respiratório superior e inferior, embora não raramente, exista comprometimento neurológico.


ABSTRACT This report aims to show an unusual case of granulomatosis with polyangeitis (GPA), previously known as Wegener's granulomatosis. It is a multisystemic disease characterized by necrotizing granulomatous inflammation and vasculitis involving mainly the upper and lower respiratory tract, although not infrequently, there is neurological impairment.


Subject(s)
Humans , Female , Adult , Granulomatosis with Polyangiitis/complications , Cranial Nerve Diseases/etiology , Sclera/transplantation , Case Reports , Methylprednisolone/therapeutic use , Magnetic Resonance Imaging , Visual Acuity , Scleritis/surgery , Granulomatosis with Polyangiitis/diagnosis , Granulomatosis with Polyangiitis/therapy , Antibodies, Antineutrophil Cytoplasmic , Cranial Nerve Diseases/diagnosis , Cranial Nerve Diseases/therapy , Cyclophosphamide/therapeutic use , Electrodiagnosis/methods
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