Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2011-5-9
pubmed:abstractText
Rosette-forming glioneuronal tumor (RGNT) of the fourth ventricle is a mixed glio-neuronal neoplasm recently codified by the World Health Organization WHO Classification of Central Nervous System (CNS) Tumors (2007). To date, 43 cases have been described in the literature; most occurring in the fourth ventricle region. We report the fourth case involving the pineal region in a 16-year-old female with signs of increased intracranial pressure (ICP). A stereotactic biopsy of the mass was followed by a debulking procedure. Both specimens revealed classic RGNT histology. The patient had stable scans 7 months post-resection. The clinical, radiological and histopathologic features of the previously described 43 cases are reviewed along with our illustrative case. Mean age of patients was 30 ± 12.8 years with 1.9:1 female to male ratio. The most common presenting signs related to increased ICP and posterior fossa involvement, including: headache (62.8%), ataxia (39.5%) and vomiting and vertigo (both 16.3%). This tumor usually presents with cystic changes (54.5%) with focal enhancement (60.9%) and hydrocephalus (43.2%). Microcalcifications and satellite lesions were common radiographic observations. All reported cases had the classic biphasic pattern. Rosenthal fibers and eosinophilic granular bodies are each present in approximately two thirds of cases. Ki-67 labeling index is consistently low (mean (%): 1.8 ± 0.75 SD). The isocitrate dehydrogenase 1 or 2 mutation found in low grade diffuse gliomas is not identified in this RGNT case. Reported outcome is nearly uniformly excellent after complete or subtotal resection. A solitary report of recurrence after 10 years and the limited experience with this entity suggest that long term follow up is advisable.
pubmed:commentsCorrections
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pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1573-7373
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
102
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
477-84
pubmed:meshHeading
pubmed-meshheading:20872044-Adolescent, pubmed-meshheading:20872044-Adult, pubmed-meshheading:20872044-Cerebral Ventricle Neoplasms, pubmed-meshheading:20872044-DNA Mutational Analysis, pubmed-meshheading:20872044-Female, pubmed-meshheading:20872044-Fourth Ventricle, pubmed-meshheading:20872044-Ganglioglioma, pubmed-meshheading:20872044-Humans, pubmed-meshheading:20872044-Intracranial Hypertension, pubmed-meshheading:20872044-Isocitrate Dehydrogenase, pubmed-meshheading:20872044-Magnetic Resonance Imaging, pubmed-meshheading:20872044-Male, pubmed-meshheading:20872044-Mutation, pubmed-meshheading:20872044-Nerve Tissue Proteins, pubmed-meshheading:20872044-Pineal Gland, pubmed-meshheading:20872044-PubMed, pubmed-meshheading:20872044-Rosette Formation, pubmed-meshheading:20872044-Young Adult
pubmed:year
2011
pubmed:articleTitle
Rosette-forming glioneuronal tumor: a pineal region case with IDH1 and IDH2 mutation analyses and literature review of 43 cases.
pubmed:affiliation
Department of Pathology and Laboratory Medicine, Section of Neuropathology, University of California, Los Angeles, Los Angeles, CA, USA. OSolis@mednet.ucla.edu
pubmed:publicationType
Journal Article, In Vitro, Review, Case Reports, Research Support, Non-U.S. Gov't