TY - JOUR
T1 - Eosinophilic vasculitis in an isolated central nervous system distribution
AU - Sommerville, R. Brian
AU - Noble, James M.
AU - Vonsattel, Jean Paul
AU - Delapaz, Robert
AU - Wright, Clinton B.
PY - 2009/2/2
Y1 - 2009/2/2
N2 - Eosinophilic vasculitis has been described as part of the Churg-Strauss syndrome, but affects the central nervous system (CNS) in <10% of cases. A 39- year-old woman with a history of migraine without aura presented to an institution in an acute conf usional state with concurrent headache and lef t-sided weakness. Laboratory evaluation showed an increased cerebrospinal fluid (CSF) protein level, but otherwise unremarkable serologies. Magnetic resonance imaging showed bif rontal polar gyral-enhancing brain lesions. Her symptoms resolved over two weeks without residual deficits. Eighteen months later the patient presented with similar symptoms and neuroradiological findings showed involvement of territories different from those in her first episode. Brain biopsy showed transmural, predominantly eosinophilic, inflammatory infiltrates and fibrinoid necrosis without granulomas. She improved when treated with corticosteroids. To our knowledge, this is the first case of non-granulomatous eosinophilic vasculitis isolated to the CNS. No aetiology for this patient's primary CNS eosinophilic vasculitis has yet been identified.
AB - Eosinophilic vasculitis has been described as part of the Churg-Strauss syndrome, but affects the central nervous system (CNS) in <10% of cases. A 39- year-old woman with a history of migraine without aura presented to an institution in an acute conf usional state with concurrent headache and lef t-sided weakness. Laboratory evaluation showed an increased cerebrospinal fluid (CSF) protein level, but otherwise unremarkable serologies. Magnetic resonance imaging showed bif rontal polar gyral-enhancing brain lesions. Her symptoms resolved over two weeks without residual deficits. Eighteen months later the patient presented with similar symptoms and neuroradiological findings showed involvement of territories different from those in her first episode. Brain biopsy showed transmural, predominantly eosinophilic, inflammatory infiltrates and fibrinoid necrosis without granulomas. She improved when treated with corticosteroids. To our knowledge, this is the first case of non-granulomatous eosinophilic vasculitis isolated to the CNS. No aetiology for this patient's primary CNS eosinophilic vasculitis has yet been identified.
UR - http://www.scopus.com/inward/record.url?scp=84897772378&partnerID=8YFLogxK
U2 - 10.1136/bcr.08.2008.0832
DO - 10.1136/bcr.08.2008.0832
M3 - Article
C2 - 21686608
AN - SCOPUS:84897772378
SN - 1757-790X
JO - BMJ Case Reports
JF - BMJ Case Reports
ER -