| Literature DB >> 27349466 |
Stylianos Pikis1, Yakov Fellig2, Emil Margolin3.
Abstract
There is limited data on the genetic origin and natural history of cerebellar liponeurocytoma. To the best of our knowledge there has been only one report of a familial presentation of this rare entity. We report a 72-year-old female with a posterior fossa tumor presenting with progressive cerebellar signs and symptoms. The patient underwent total tumor resection via an uncomplicated sub-occipital craniotomy. Histopathologic examination was diagnostic for cerebellar liponeurocytoma. Her sister was previously treated for a similar tumor. Our report provides further evidence for the possible existence of a hereditary abnormality predisposing afflicted families to cerebellar liponeurocytoma development.Entities:
Keywords: Biology; Cerebellar liponeurocytomas; Familial; Inheritance
Mesh:
Year: 2016 PMID: 27349466 DOI: 10.1016/j.jocn.2016.04.004
Source DB: PubMed Journal: J Clin Neurosci ISSN: 0967-5868 Impact factor: 1.961