Open AccessHypertrophic pachymeningitis and orbital tumor associated with Granulomatosis with polyangiitis: report of a clinical case
Author(s) -
S. Argüello,
M. Avatte,
Renato V. LaRocca,
R. Movía
Publication year - 2021
Publication title -
revista argentina de reumatología
Language(s) - English
Resource type - Journals
eISSN - 2362-3675
pISSN - 0327-4411
DOI - 10.47196/rar.v32i1.367
Subject(s) - medicine , granulomatosis with polyangiitis , refractory (planetary science) , magnetic resonance imaging , cyclophosphamide , azathioprine , surgery , vasculitis , dermatology , radiology , disease , chemotherapy , physics , astrobiology
A 65-year-old patient, with a diagnosis of Granulomatosis with Polyangeitis (GPA) of 18 years of evolution, whose debut was with respiratory failure and hemoptysis, receiving induction treatment with corticosteroids together with cyclophosphamide, and then maintenance treatment with azathioprine 150 mg per day, with periods of flare-up of the disease that responded to treatment with corticosteroids for short periods. He came to the clinic for a 3-month-long chronic headache refractory to treatment with non-steroidal anti-inflammatory drugs (NSAIDs), associated with left ocular proptosis and ipsilateral orbital pain. presenting elevated acute phase reactants (ers and c-reactive protein). It is evidenced by brain magnetic resonance with gadolinium, enhancement of the cerebral dura and cerebellum store, also presenting formation in the left orbit.