| Literature DB >> 23925681 |
Nikhil Huprikar1, Marisa Gossweiler, Maureen Callaghan, Paul Bunge.
Abstract
Superficial siderosis of the central nervous system is a rare neurological disorder caused by deposits of haemosiderin on subplial brain matter. Characterised by a thin dark layer surrounding the brain stem, cerebellum and cortical fissures on the T2-weighted MRI, symptoms include sensorineural hearing loss and progressive gait ataxia. A specific aetiology for the blood in the subarachnoid space is identified in less than 50% of cases. While identification of a specific vascular defect allows for vascular repair, treatment options are limited for idiopathic superficial siderosis. Recently, a pilot safety study demonstrated promising results using an iron chelator, deferiprone. While this approach is promising, we present a potential serious complication of this therapy-the first report of agranulocytosis in the treatment of superficial siderosis following deferiprone therapy.Entities:
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Year: 2013 PMID: 23925681 PMCID: PMC3762355 DOI: 10.1136/bcr-2013-010099
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X