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CC BY 4.0 · Indian Journal of Neurosurgery 2024; 13(01): 076-080
DOI: 10.1055/s-0042-1743263
Case Report

Primary Central Nervous System Angiitis Mimicking a Space-Occupying Lesion

Edmond Jonathan Gandham
1   Division of Neurosurgery, Department of Neurological Sciences, Christian Medical College, Vellore, India
,
Bimal Patel
2   Department of Pathology, Christian Medical College, Vellore, India
,
Vivek Mathew
3   Division of Neurology, Department of Neurological Sciences, Christian Medical College, Vellore, India
,
Krishna Prabhu Raju
1   Division of Neurosurgery, Department of Neurological Sciences, Christian Medical College, Vellore, India
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Abstract

Background and Purpose Intracranial space-occupying lesions are a sine qua non for neoplastic lesions; however, occasionally non-neoplastic lesions mimic neoplastic lesions, leading to diagnostic dilemmas. We report our experience with three patients who presented with a progressive hemispheric syndrome and the diagnostic considerations involved in the cases.

Materials and Methods In this retrospective study, we included three patients with primary angiitis of central nervous system (PACNS) who underwent craniotomy and biopsy, suspecting it to be mass lesions. Demographic features, clinical features, radiological features, histopathology, treatment, and clinical outcomes were studied.

Results Majority were males. The male:female ratio was 2:1. Lobar involvement was common. MR brain with contrast showed features of high-grade glioma. Despite hemispheric involvement, there was no mass effect. Perilesional edema was seen in all cases. All underwent craniotomy and biopsy; histopathology was consistent with PACNS. All patients were treated with corticosteroids and cyclophosphamide. Rituximab was used in addition to cyclophosphamide in one patient. At 2 years follow-up, two patients were in disease remission and one patient died due to disease progression.

Conclusion PACNS has a protean clinical manifestation. A high index of suspicion is required in cases with atypical clinical presentations, radiological features, and normal angiograms. Early histological diagnosis and aggressive immunotherapy with high-dose corticosteroids combined with intravenous cyclophosphamide yields favorable outcomes.

Keywords

primary CNS angiitis - craniotomy - corticosteroids - cyclophosphamide

Ethical Approval Statement

This study has been approved by institutional review board, Christian Medical College, Vellore, India.


Authors' Contribution

K.P.R. contributed in the concept and design of study; E.J.G., B.P., and V.M. in data collection and analysis; E.J.G. and V.M. in manuscript preparation; K.P.R. and V.M. in the critical revision of manuscript; and K.P.R. as guarantor.




Publication History

Article published online:
16 May 2022

© 2022. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

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