| Literature DB >> 30121405 |
Adrien Collin1, Homa Adle-Biassette2, Augustin Lecler3.
Abstract
Rosette-forming glioneuronal tumor has recently been included in the World Health Organization classification as a low-grade tumor. It usually occurs in young adults, arising from the fourth ventricular region. The authors describe a rare case of rosette-forming glioneuronal tumor arising from the spinal cord with cerebrospinal fluid dissemination. Magnetic resonance imaging showed a cervical spinal cord tumor, which could be easily misdiagnosed as ependyma or astrocytoma. Surgical total resection was performed, and histopathologic examination made the diagnosis, showing a biphasic neurocytic and glial tumor with neurocytic rosettes. Six months after surgery, the patient had fully recovered.Entities:
Keywords: MRI; RGNT; Rosette-forming glioneuronal tumor; Spinal; Tumor
Mesh:
Year: 2018 PMID: 30121405 DOI: 10.1016/j.wneu.2018.08.035
Source DB: PubMed Journal: World Neurosurg ISSN: 1878-8750 Impact factor: 2.104