Supratentorial PNET

2016 ◽  
pp. 540-543
Keyword(s):  
2018 ◽  
Vol 20 (suppl_2) ◽  
pp. i162-i162
Author(s):  
Karin Walsh ◽  
Eugene Hwang ◽  
Kristina Hardy ◽  
Leanne Embry ◽  
Anthony Gioia ◽  
...  

2001 ◽  
Vol 37 ◽  
pp. S265
Author(s):  
B. Timmermann ◽  
R.-D. Kortmann ◽  
J. Kühl ◽  
M. Bamberg
Keyword(s):  

2006 ◽  
Vol 48 (5) ◽  
pp. 579-587 ◽  
Author(s):  
M M Inda ◽  
J Munoz ◽  
P Coullin ◽  
D Fauvet ◽  
G Danglot ◽  
...  

2020 ◽  
pp. 452-454
Author(s):  
Hrushikesh Kharosekar ◽  
Laxmikant Bhople ◽  
Reshma Pujara ◽  
Smita Ranveer

Supratentorial PNETs are most commonly seen in children and rarely seen in adults. PNET show a proliferation of undifferentiated or poorly differentiated neuroepithelial cells and, thus, are histologically similar to medulloblastomas. They account for approximately 2.5% of brain tumours in children and only 0.4% in adults. Prognosis is poor in the pediatric age group while it shows favourable prognosis in adults. In literature, less than 100 cases of adult PNET have been reported till date with mean age of 35years. PNET in the geriatric age group is rarely been reported


2007 ◽  
Vol 29 (12) ◽  
pp. 832-835 ◽  
Author(s):  
Friederike Blankenburg ◽  
Frank K. H. van Landeghem ◽  
Michail Plotkin ◽  
Günter Henze ◽  
Andreas von Deimling ◽  
...  

2021 ◽  
Vol 69 (6) ◽  
pp. 1855
Author(s):  
Ishu Bishnoi ◽  
Pardaman Singh ◽  
Karandeep Singh ◽  
Geetika Duggal ◽  
Sanjeev Kumar ◽  
...  

2005 ◽  
Vol 19 (5) ◽  
pp. 1-17 ◽  
Author(s):  
Mei Hua Li ◽  
Eric Bouffet ◽  
Cynthia E. Hawkins ◽  
Jeremy A. Squire ◽  
Annie Huang

The supratentorial primitive neuroectodermal tumors (PNETs) are a group of highly malignant lesions primarily affecting young children. Although these tumors are histologically indistinguishable from infratentorial medulloblastoma, they often respond poorly to medulloblastoma-specific therapy. Indeed, existing molecular genetic studies indicate that supratentorial PNETs have transcriptional and cytogenetic profiles that are different from those of medullo-blastomas, thus pointing to unique biological derivation for the supratentorial PNET. Due to the rarity of these tumors and disagreement about their histopathological diagnoses, very little is known about the molecular characteristics of the supratentorial PNET. Clearly, future concerted efforts to characterize the molecular features of these rare tumors will be necessary for development of more effective supratentorial PNET treatment protocols and appropriate disease models. In this article the authors review existing molecular genetic data derived from human and mouse studies, with the aim of providing some insight into the putative histogenesis of these rare tumors and the underlying transforming pathways that drive their development. Studies of the related but distinct pineoblastoma PNET are also reviewed.


2011 ◽  
Vol 8 (5) ◽  
pp. 468-475 ◽  
Author(s):  
Pinakin R. Jethwa ◽  
Jason H. Lee ◽  
Rachid Assina ◽  
Irwin A. Keller ◽  
Shabbar F. Danish

Supratentorial primitive neuroectodermal tumors (PNETs) are rare tumors that carry a poorer prognosis than those arising from the infratentorial compartment (such as medulloblastoma). The overall prognosis for these patients depends on several factors including the extent of resection, age at diagnosis, CSF dissemination, and site in the supratentorial space. The authors present the first case of a patient with a newly diagnosed supratentorial PNET in which cytoreduction was achieved with MR-guided laser-induced thermal therapy. A 10-year-old girl presented with left-sided facial weakness and a large right thalamic mass extending into the right midbrain. The diagnosis of supratentorial PNET was made after stereotactic biopsy. Therapeutic options for this lesion were limited because of the risks of postoperative neurological deficits with resection. The patient underwent MR-guided laser-induced thermal ablation of her tumor. Under real-time MR thermometry, thermal energy was delivered to the tumor at a core temperature of 90°C for a total of 960 seconds. The patient underwent follow-up MR imaging at regular intervals to evaluate the tumor response to the thermal ablation procedure. Initial postoperative scans showed an increase in the size of the lesion as well as the amount of the associated edema. Both the size of the lesion and the edema stabilized by 1 week and then decreased below preablation levels at the 3-month postsurgical follow-up. There was a slight increase in the size of the lesion and associated edema at the 6-month follow-up scan, presumably due to concomitant radiation she received as part of her postoperative care. The patient tolerated the procedure well and has had resolution of her symptoms since surgery. Further study is needed to assess the role of laser-induced thermal therapy for the treatment of intracranial tumors. As such, it is a promising tool in the neurosurgical armamentarium. Postoperative imaging has shown no evidence of definitive recurrence at the 6-month follow-up period, but longer-term follow-up is required to assess for late recurrence.


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