Literature DB >> 26720861

Gliofibroma: Report of Four Cases and Review of the Literature.

Marta Celina Jones1, Verónica Díaz2, Marcelo D'Agustini3, Eugenia Altamirano4, Natalia Baglieri1, Ricardo Drut5.   

Abstract

Gliofibroma is a relatively rare variant of a mixed glial-fibrous tumor more frequent in children than in adults. It has been reported to appear all along the neuraxis, with predilection for the midline. Its evolution is usually benign, although few examples have shown either multiple sites of involvement or leptomeningeal dissemination. Some authors regard it as part of the desmoplastic astrocytoma spectrum. We report here four examples of this rare condition which exemplify its histological patterns and biological behavior, and provide a review of the literature. Even though this tumor is commonly regarded as heterogeneous and with variable course, our literature review points to a set of clinical and pathological traits that are constant, such as age, location and gross and histological characteristics, as well as a predictable evolution. Currently, this tumor is not included in the WHO Classification of CNS tumors.

Entities:  

Keywords:  brain tumor; desmoplastic astrocytoma; gliofibroma; spinal cord tumor

Mesh:

Year:  2015        PMID: 26720861     DOI: 10.3109/15513815.2015.1122124

Source DB:  PubMed          Journal:  Fetal Pediatr Pathol        ISSN: 1551-3815            Impact factor:   0.958


  2 in total

1.  Rare Pediatric Invasive Gliofibroma Has BRAFV600E Mutation and Transiently Responds to Targeted Therapy Before Progressive Clonal Evolution.

Authors:  Kristiyana Kaneva; Kee Kiat Yeo; Debra Hawes; Jianling Ji; Jaclyn A Biegel; Marvin D Nelson; Stefan Bluml; Mark D Krieger; Anat Erdreich-Epstein
Journal:  JCO Precis Oncol       Date:  2019-03-27

2.  Successful Treatment of a Massive Desmoplastic Fibroma of the Ilium without Surgery: A Case Report with Long-Term Follow-Up.

Authors:  Hideyuki Kinoshita; Takeshi Ishii; Hiroto Kamoda; Yoko Hagiwara; Toshinori Tsukanishi; Sumihisa Orita; Kazuhide Inage; Naoya Hirosawa; Seiji Ohtori; Tsukasa Yonemoto
Journal:  Case Rep Orthop       Date:  2020-03-20
  2 in total

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