Benign glioneuronal tumor with unique histological features presenting with intractable epilepsy

2007 ◽  
Vol 86 (2) ◽  
pp. 239-240
Author(s):  
Kelly Dakin-Haché ◽  
David B. Clarke ◽  
Alexander S. Easton
2017 ◽  
Vol 3 ◽  
pp. 227-234 ◽  
Author(s):  
Blanka Hermann ◽  
Michal Woznica ◽  
Wojciech Kloc ◽  
Piotr Borkowski ◽  
Witold Libionka ◽  
...  

2009 ◽  
Vol 117 (5) ◽  
pp. 591-593 ◽  
Author(s):  
Martin Scholz ◽  
Alexander Hoischen ◽  
Bernhard Radlwimmer ◽  
Ruthild G. Weber ◽  
Albrecht Harders ◽  
...  

2012 ◽  
Vol 2 ◽  
pp. 60 ◽  
Author(s):  
Harsha Guduru ◽  
Jun K. Shen ◽  
Harish S. Lokannavar

We present a rare case of dysembryoplastic neuroepithelial tumor, a rare benign glioneuronal tumor of the central nervous system. It generally occurs in the supratentorial region and the temporal cerebral cortex in children and young adults. The most common presentation is epilepsy. The supratentorial tumor without any signs of mass effect or peritumoral edema is the conventionally accepted diagnostic criteria. In this case of a 19-year-old male with intractable epilepsy, atypical features such as the location of the tumor and the presence of mass effect and peritumoral edema made imaging diagnosis difficult. Diagnosis was confirmed through histopathology. Due to its recent discovery and relatively rare occurrence it is important for radiologists to recognize this disease entity.


Neurosurgery ◽  
2009 ◽  
Vol 64 (6) ◽  
pp. E1193-E1195 ◽  
Author(s):  
Jian-Qiang Lu ◽  
Bernd W. Scheithauer ◽  
Pranshu Sharma ◽  
James N. Scott ◽  
Ian F. Parney ◽  
...  

Abstract OBJECTIVE The clinicopathological spectra of a dysembryoplastic neuroepithelial tumor (DNT) and a rosette-forming glioneuronal tumor (RGNT) are expanding. We report here the autopsy findings of a case of complex glioneuronal tumor with combined histological features of both a DNT and an RGNT. CLINICAL PRESENTATION A 79-year-old man presented with a 1-month history of confusion and gait difficulties. A magnetic resonance imaging scan revealed obstructive hydrocephalus attributed to a mass in the posterior third ventricle. INTERVENTION A third ventriculostomy was performed. Postoperatively, the mass remained unchanged in size for more than 14 months. Thirty-eight months after his initial manifestations, he experienced minor head trauma and was then hospitalized. Despite placement of an external ventricular drain and other supportive treatment, he deteriorated and died. A full autopsy was performed, with emphasis on the brain. The mass lesion and a few independent microfoci situated primarily around the third ventricle showed histological features of pilocytic astrocytoma with recurrent hemorrhage. Far more numerous were microfoci with histological features of a DNT, including floating neurons, as well as typical RGNT-associated, synaptophysin-positive rosettes and perivascular pseudorosettes. CONCLUSION The advanced age of the patient, the coexisting histological features of the DNT and RGNT, and the distinctive anatomic distribution of the lesions, being centered on the third ventricle, may lend insight into the histogenetic relationship of a DNT, an RGNT, and mixed glioneuronal tumors.


2017 ◽  
Vol 38 (3) ◽  
pp. 300-304 ◽  
Author(s):  
Noriko Sumitomo ◽  
Akihiko Ishiyama ◽  
Makoto Shibuya ◽  
Eiji Nakagawa ◽  
Yu Kaneko ◽  
...  

2000 ◽  
Vol 31 (11) ◽  
pp. 1435-1438
Author(s):  
Richard A. Prayson ◽  
Caroline M. Abramovich
Keyword(s):  

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