ArticleJournal of neurology2009
Isolated angiitis of the CNS and bacterial endocarditis: similarities and differences.
Article in Journal of neurology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed, 29 citations in OpenAlex.
- Primary angiitis of the CNS (PACNS) and Behçet disease.Neurological research and practice · 2019Article
- Diagnostic test results in primary CNS vasculitis: A systematic review of published cases.Neurology. Clinical practice · 2017Review
- Cerebral vasculitis in adults: what are the steps in order to establish the diagnosis? Red flags and pitfalls.Clinical and experimental immunology · 2014Review
- The spectrum of CNS vasculitis in children and adults.Nature reviews. Rheumatology · 2011Review
- The diagnostic conundrum of primary angiitis of the central nervous system: a case report.Journal of neurology · 2011Article
- [Reversible cerebral vasoconstriction syndrome vs cerebral vasculitis? On the importance and difficulty of differentiating].Der Nervenarzt · 2011Article
- Primary central nervous system vasculitis: clinical experiences with 21 new European cases.Rheumatology international · 2011Article
- Infectious vasculopathy of intracranial large- and medium-sized vessels in neurological intensive care unit: a clinico-radiological study.Neurocritical care · 2010Article
- Primary central nervous system vasculitis and moyamoya disease: similarities and differences.Journal of neurology · 2010Article
- [Vasculitis of the nervous system in infectious diseases].Der Nervenarzt · 2010Review
- Diagnosis and treatment of cerebral vasculitis.Therapeutic advances in neurological disorders · 2010Article
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Authors and funding
1 author at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Both isolated angiitis of the central nervous system (IAN) and bacterial endocarditis (BE) may present with similar clinical and auxiliary findings. The differentiation is extremely important because of the different treatment regimens. We compared the findings of six patients with biopsy-proven IAN with the data of six patients with BE. Patients with IAN were younger (27-62 years) and presented with multiple strokes (n = 4), intracerebral hemorrhage (n = 1), epileptic seizures (n = 2), or encephalopathy (n = 1). All IAN patients had pathologic cerebrospinal fluid (CSF) findings (pleocytosis n = 5; protein elevation n = 4), and angiography revealed multilocular stenoses in two cases while digital subtraction angiography was normal in four. BE patients (32-77 years) presented multiple (n = 3) or single ischemic strokes (n = 2) or encephalopathy and headache (n = 2). While all patients showed inflammatory serum findings (C-reactive protein n = 6, leucocytosis n = 4), CSF-pleocytosis was present in two cases only. Angiography revealed a vasculitic pattern in two patients. The diagnosis of BE was established based on transesophageal echocardiography and blood cultures. Leptomeningeal and brain biopsies performed in two cases were normal. Both IAN and BE may present multiple strokes and encephalopathy. The frequency of a vasculitic pattern in angiography is similar in both conditions. While inflammatory serum findings are the rule in BE, pathologic CSF findings were present in all IAN patients. Transesophageal echocardiography and blood cultures should be performed in order to diagnose or exclude BE. Without brain biopsy, immunosuppressive therapy may be dangerous in suspected IAN.
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