A Presentation of Cerebritis Secondary to Granulomatosis with Polyangiitis (Wegener)

Neurological manifestations of GPA are common, most frequently as a peripheral neuropathy. Cerebritis as a principal presentation is extremely rare. We report a patient who presented with subacute progression of ataxia, confusion, and vacant episodes. An MRI of her brain showed bilateral signal abno...

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Main Authors: James Norman, Ira Pande, Timothy Taylor, Bruno Gran
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:Case Reports in Neurological Medicine
Online Access:http://dx.doi.org/10.1155/2014/914530
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author James Norman
Ira Pande
Timothy Taylor
Bruno Gran
author_facet James Norman
Ira Pande
Timothy Taylor
Bruno Gran
author_sort James Norman
collection DOAJ
description Neurological manifestations of GPA are common, most frequently as a peripheral neuropathy. Cerebritis as a principal presentation is extremely rare. We report a patient who presented with subacute progression of ataxia, confusion, and vacant episodes. An MRI of her brain showed bilateral signal abnormalities in the cingulate and superior sagittal gyrus while a staging CT revealed a mass in the right upper lobe of the patient’s lung with a satellite nodule. C-ANCA antibodies specific for PR3 at high titres were positive and a diagnosis of GPA was made. The patient was commenced on intravenous methylprednisolone followed by cyclophosphamide and responded well to treatment. GPA is a rare and treatable differential diagnosis for confused patients with acute or subacute neurological features and unusual MRI findings.
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spelling doaj-art-3d420f60edef46a2bd6916af3300b5d32025-02-03T01:20:22ZengWileyCase Reports in Neurological Medicine2090-66682090-66762014-01-01201410.1155/2014/914530914530A Presentation of Cerebritis Secondary to Granulomatosis with Polyangiitis (Wegener)James Norman0Ira Pande1Timothy Taylor2Bruno Gran3Department of Neurology, Nottingham University Hospitals NHS Trust, Queen's Medical Centre Campus, Nottingham NG7 2UH, UKDepartment of Rheumatology, Nottingham University Hospitals NHS Trust, Queen’s Medical Centre Campus, Nottingham NG7 2UH, UKDepartment of Radiology, Nottingham University Hospitals NHS Trust, Queen’s Medical Centre Campus, Nottingham NG7 2UH, UKDepartment of Neurology, Nottingham University Hospitals NHS Trust, Queen's Medical Centre Campus, Nottingham NG7 2UH, UKNeurological manifestations of GPA are common, most frequently as a peripheral neuropathy. Cerebritis as a principal presentation is extremely rare. We report a patient who presented with subacute progression of ataxia, confusion, and vacant episodes. An MRI of her brain showed bilateral signal abnormalities in the cingulate and superior sagittal gyrus while a staging CT revealed a mass in the right upper lobe of the patient’s lung with a satellite nodule. C-ANCA antibodies specific for PR3 at high titres were positive and a diagnosis of GPA was made. The patient was commenced on intravenous methylprednisolone followed by cyclophosphamide and responded well to treatment. GPA is a rare and treatable differential diagnosis for confused patients with acute or subacute neurological features and unusual MRI findings.http://dx.doi.org/10.1155/2014/914530
spellingShingle James Norman
Ira Pande
Timothy Taylor
Bruno Gran
A Presentation of Cerebritis Secondary to Granulomatosis with Polyangiitis (Wegener)
Case Reports in Neurological Medicine
title A Presentation of Cerebritis Secondary to Granulomatosis with Polyangiitis (Wegener)
title_full A Presentation of Cerebritis Secondary to Granulomatosis with Polyangiitis (Wegener)
title_fullStr A Presentation of Cerebritis Secondary to Granulomatosis with Polyangiitis (Wegener)
title_full_unstemmed A Presentation of Cerebritis Secondary to Granulomatosis with Polyangiitis (Wegener)
title_short A Presentation of Cerebritis Secondary to Granulomatosis with Polyangiitis (Wegener)
title_sort presentation of cerebritis secondary to granulomatosis with polyangiitis wegener
url http://dx.doi.org/10.1155/2014/914530
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