Papillary Glioneuronal Tumor: A Case Report and a Brief Review

Author(s):  
Amir Jafarian ◽  
Nema Roshan ◽  
Abbas Omidi ◽  
Samaneh Boroumand-Noughabi
2006 ◽  
Vol 37 (7) ◽  
pp. 914-918 ◽  
Author(s):  
Daniel C. Dim ◽  
Daniel C. Lingamfelter ◽  
Eugenio M. Taboada ◽  
Russell M. Fiorella

2012 ◽  
Vol 31 (03) ◽  
pp. 77-80 ◽  
Author(s):  
Thomas Flannery ◽  
Andrew Purce ◽  
Jacqueline Harney ◽  
Steven McKinstry ◽  
James W. Ironside ◽  
...  

2018 ◽  
Vol 2018 (6) ◽  
Author(s):  
Yuya Fujita ◽  
Manabu Kinoshita ◽  
Tomohiko Ozaki ◽  
Masanori Kitamura ◽  
Shin-ichi Nakatsuka ◽  
...  

2008 ◽  
Vol 27 (09) ◽  
pp. 317-324 ◽  
Author(s):  
H.B. Newton ◽  
J. Dalton ◽  
A. Ray-Chaudhury ◽  
R. Gahbauer ◽  
J. McGregor

Author(s):  
Hillary Sayuri Ramires Hoshino ◽  
Bruna Grazielle Silva dos Santos ◽  
Adriano Barreto Nogueira ◽  
Antonio Celso Alvarenga Guimarães

Author(s):  
Sameer Peer ◽  
Vivek Murumkar ◽  
Karthik Kulanthaivelu ◽  
Chandrajit Prasad ◽  
Shilpa Rao ◽  
...  

Abstract Background Diffuse leptomeningeal glioneuronal tumor (DLGNT) has been recently described in the literature. The complete neuroimaging spectrum and histopathological characteristics of this entity are yet to be elucidated. In an endemic region, diffuse leptomeningeal enhancement on neuroimaging with associated communicating hydrocephalus is usually suggestive of infective meningitis and the patients are started on empirical anti-microbial therapy. However, it is important to consider other differential diagnosis of leptomeningeal enhancement in such cases, particularly if the clinical condition does not improve on anti-microbial therapy. An early diagnosis of a neoplastic etiology may be of particular importance as the treatment regimens vary considerably depending on the underlying disease condition. Case presentation In this case report, we describe a case of DLGNT with high-grade histopathological features which was initially managed as tubercular meningitis based on the initial neuroimaging findings. Due to worsening of the clinical course and subsequent imaging findings at follow-up, a diagnosis of DLGNT was considered and subsequently proven to be DLGNT with features of anaplasia on histopathological examination of leptomeningeal biopsy specimen. Conclusion This case highlights the importance of recognizing certain subtle finding on MRI which may help in an early diagnosis of DLGNT which is crucial for appropriate treatment.


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