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DOI: 10.1055/s-0034-1368285
Small-Cell Lung Carcinoma Presenting as Paraneoplastic Autoimmune Optic Neuritis with Retinitis
Kleinzelliges Lungenkarzinom präsentiert sich als paraneoplastische autoimmune optische Neuritis mit RetinitisPublication History
Publication Date:
25 April 2014 (online)
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Background
Optic neuritis associated with retinitis and severe vitreous inflammation is a challenging diagnostic problem. Clinical findings appear similar or identical in various inflammatory conditions such as ischemic neuropathy, large B cell lymphoma, demyelinating disease, severe uveitis, or paraneoplastic disorders [1].
Paraneoplastic optic neuritis is an ocular manifestation of systemic neoplasia that is clinically characterized by subacute vision reduction, optic discs swelling and neurological symptoms. In this contest, two auto-antibodies have been described in order to define two of the most important paraneoplastic syndromes which involve the eye: CAR-IgG directed against recoverin (“carcinoma-associated retinopathy”) and CRMP-5-IgG (“collapsin response-mediator protein 5”) [2]. The latter defines a paraneoplastic ophthalmological entity combining optic neuritis, retinitis and vitreous inflammatory cells.
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References
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- 2 Cross SA, Salomao DR, Parisi JE et al. Paraneoplastic autoimmune optic neuritis with retinitis defined by CRMP-5-IgG. Ann Neurol 2003; 54: 38-50
- 3 Damek DM. Paraneoplastic retinopathy/optic neuropathy. Curr Treat Options Neurol 2005; 7: 57-67
- 4 Shiraga S, Adamus G. Mechanism of CAR syndrome: anti-recoverin antibodies are the inducers of retinal cell apoptotic death via the caspase 9- and caspase 3-dependent pathway. J Neuroimmunol 2002; 132: 72-82
- 5 Murphy MA, Thirkill CE, Hart jr. WM. Paraneoplastic retinopathy: a novel autoantibody reaction associated with small-cell lung carcinoma. J Neuroophthalmol 1997; 17: 77-83