| Literature DB >> 23899665 |
Marina Frasquet1, Luis Bataller, Estefanía Torres-Vega, María Durán-Moreno, José M García-Verdugo, Teresa Sevilla, Salvador Rivas, Francisco Pérez-Miralles, María Simó-Castelló, Bonaventura Casanova.
Abstract
Paraneoplastic myelitis is a rare inflammatory disorder most frequently associated with solid tumors or lymphoproliferative disorders. Patients often harbor onconeuronal antibodies and their prognosis is usually poor. Here we report a 42-year old woman with longitudinally extensive transverse myelitis and aquaporin-4 (AQP4) antibodies that led to the diagnosis of ovarian teratoma. After tumor removal and immune therapy (including corticosteroids, plasma exchange, intravenous immunoglobulins and rituximab) the patient progressively improved achieving complete recovery. Histological study of the teratoma demonstrated neural tissue containing AQP4 expressing cells and intense inflammatory infiltrates, providing evidence for a possible paraneoplastic link between both disorders.Entities:
Keywords: Autoimmune diseases; Paraneoplastic syndrome; Transverse myelitis
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Year: 2013 PMID: 23899665 DOI: 10.1016/j.jneuroim.2013.07.003
Source DB: PubMed Journal: J Neuroimmunol ISSN: 0165-5728 Impact factor: 3.478