| Literature DB >> 31951480 |
Chenue Abongwa1, Jennifer Cotter2, Benita Tamrazi3, Girish Dhall4, Tom Davidson5, Ashley Margol5.
Abstract
Primary diffuse leptomeningeal glioneuronal tumors (DLGNT) are rare tumors, recently recognized as a unique entity based on their unique pathologic and clinical characteristics. We report three cases of DLGNT and compare their clinical characteristics and presentation with other reported cases, and with primary leptomeningeal gliomatosis. Because their prognosis is better than that of diffuse leptomeningeal gliomatosis, and pathologic diagnosis may be difficult, clinicians should consider this diagnosis in patients who present with new neurological symptoms, hydrocephalus and diffuse leptomeningeal enhancement on MRI. Further studies are required to better understand the unique biological characteristics of these tumors and to improve therapy.Entities:
Keywords: Astrocytoma; glial; glioneuronal; hydrocephalus; leptomeningeal
Year: 2020 PMID: 31951480 DOI: 10.1080/08880018.2019.1711270
Source DB: PubMed Journal: Pediatr Hematol Oncol ISSN: 0888-0018 Impact factor: 1.969