Literature DB >> 19521134

A case report of intraventricular gliofibroma.

Rajashree Sarkar1, William H Yong, Jorge A Lazareff.   

Abstract

Gliofibroma is a rare tumor with biphasic morphology. We report a case of a 3-month-old girl presenting with increasing head circumference. CT and MRI showed the presence of a large heterogeneous, nonenhancing tumor filling the atria and bodies of the lateral ventricles with caudal extension into the third ventricle. Hydrocephalus was noted. A biopsy was performed and pathology showed the presence of glial and collagenous tissue consistent with the diagnosis of gliofibroma. However, no mitosis or necrosis was seen. Immunohistochemistry was positive for glial fibrillary acid protein, Masson trichrome and reticulin. The patient was followed up for a period of 10 years. Recent MRI showed stable appearance of the tumor and clinically the patient is neurologically intact with normal cognitive development. Our case report has the longest follow-up so far reported in the literature, of 10 years. As evident from our case report, we recommend a conservative treatment approach for gliofibroma with benign histology. Copyright 2009 S. Karger AG, Basel.

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Year:  2009        PMID: 19521134     DOI: 10.1159/000224617

Source DB:  PubMed          Journal:  Pediatr Neurosurg        ISSN: 1016-2291            Impact factor:   1.162


  3 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.  Intracranial gliofibroma: a case report and review of the literature.

Authors:  Patricia Gargano; Graciela Zuccaro; Fabiana Lubieniecki
Journal:  Case Rep Pathol       Date:  2014-07-13

3.  Adult Intracranial Gliofibroma : A Case Report and Review of the Literature.

Authors:  Ho Kang; Jin Wook Kim; Young-Bem Se; Sung-Hye Park
Journal:  J Korean Neurosurg Soc       Date:  2016-05-10
  3 in total

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