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pubmed-article:1832307pubmed:abstractTextThe course of a patient suffering from superficial siderosis of the central nervous system for 37 years is presented and diagnostic and therapeutic approaches are evaluated. The syndrome is clinically defined by slowly progressing deafness, cerebellar ataxia, myelopathy and neuropsychological deficits in combination with recurrent xanthochromia of the cerebrospinal fluid with siderophages. The diagnosis may be confirmed by computed tomography, which shows degeneration of the cerebellar vermis, and by magnetic resonance imaging, demonstrating iron deposits on the surface of brain, brain stem and spinal cord. Therapy should seek to identify and remove the source of bleeding, since pharmacotherapy with iron-depleting drugs is of limited effectiveness.lld:pubmed
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pubmed-article:1832307pubmed:pagination57-60lld:pubmed
pubmed-article:1832307pubmed:dateRevised2009-5-11lld:pubmed
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pubmed-article:1832307pubmed:year1991lld:pubmed
pubmed-article:1832307pubmed:articleTitleSuperficial siderosis of the central nervous system. A 37-year follow-up of a case and review of the literature.lld:pubmed
pubmed-article:1832307pubmed:affiliationDepartment of Neurology, University of Tübingen, Federal Republic of Germany.lld:pubmed
pubmed-article:1832307pubmed:publicationTypeJournal Articlelld:pubmed
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