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A rare case of tumor-mimicking primary angiitis of the central nervous system
Author(s) -
Li Sun,
Lijun Zhu,
Teng Zhao,
Dayan Wang,
Dihui Ma,
Zhang Ren-sheng,
Shaokuan Fang
Publication year - 2016
Publication title -
molecular and clinical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.442
H-Index - 7
eISSN - 2049-9469
pISSN - 2049-9450
DOI - 10.3892/mco.2016.784
Subject(s) - medicine , vasculitis , pathological , magnetic resonance imaging , cerebral vasculitis , cyclophosphamide , radiology , lesion , pathology , glioma , central nervous system , disease , chemotherapy , surgery , cancer research
Primary angiitis of the central nervous system (PACNS) is a rare, but severe vascular disease. The present study reports the case of a 42-year-old male who developed PACNS. Magnetic resonance imaging (MRI) scans initially led to a misleading diagnosis of malignant glioma, and surgery was performed. The mass was resected, and a pathological examination confirmed a cerebral vasculitis. Single therapy with high doses of steroid did not improve the patient's condition, while a subsequent lesion appeared on the opposite side one year later. Combined therapy with methylprednisone and cyclophosphamide resulted in a great improvement for the patient. No relapse occurred during one year's follow-up. Although a tumor-mimicking PACNS has no established imaging features, a diagnosis of tumor-mimicking PACNS should be suspected when the MRI reveals inappropriate presentations of a tumor. Greater awareness of this potential manifestation of PACNS may facilitate more prompt diagnosis and treatment.

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