| Literature DB >> 27083067 |
Philippe Joaquim Oliveira Menezes Macêdo1, Victor Calil da Silveira2, Luíza Tavares Ramos2, Felipe Resende Nóbrega2, Luiz Felipe Rocha Vasconcellos2.
Abstract
A 62-year-old male presented to our clinic with recurrent fever, skin lesions (petechiae), scleral wounds, and hilar adenomegaly. A diagnosis of sarcoidosis was established, which resolved with corticosteroid treatment. After a few months, the patient developed confusion and behavioral changes, with few objective neurological deficits. Brain magnetic resonance imaging showed slight focal meningeal enhancement (prepontine region). The level of angiotensin-converting enzymes was normal in the serum and increased in the cerebrospinal fluid. The patient was diagnosed with neurosarcoidosis, and corticosteroid treatment was prescribed, yielding good clinical response. Nine months later, the patient presented with multiple ischemic strokes, and arteriography demonstrated multiple distal irregularities in all arterial territories, suggesting cerebral vasculitis. Even with corticosteroids, cyclophosphamide, and intravenous immunoglobulin, the patient died. Vasculitis is rarely seen in association with sarcoidosis, and in this case, no systemic manifestation was observed at the time that the patient developed vasculitis.Entities:
Keywords: Sarcoidosis; angiitis; neurosarcoidosis; vasculitis
Mesh:
Substances:
Year: 2016 PMID: 27083067 DOI: 10.1016/j.jstrokecerebrovasdis.2016.02.036
Source DB: PubMed Journal: J Stroke Cerebrovasc Dis ISSN: 1052-3057 Impact factor: 2.136