Abstract C111: Pediatric Preclinical Testing Program (PPTP): Evaluation of the MEK1/2 inhibitor AZD6244 against juvenile pilocytic astrocytoma (JPA) xenografts

Author(s):  
Malcolm A. Smith ◽  
Christopher L. Morton ◽  
Doris Phelps ◽  
Geoffrey A. Neale ◽  
Peter J. Houghton
2012 ◽  
Vol 224 (06) ◽  
Author(s):  
T Milde ◽  
M Zucknick ◽  
M Kool ◽  
A Korshunov ◽  
H Witt ◽  
...  

2014 ◽  
Vol 50 ◽  
pp. 131 ◽  
Author(s):  
M. Smith ◽  
M. Kang ◽  
P. Reynolds ◽  
R. Lock ◽  
H. Carol ◽  
...  

1978 ◽  
Vol 49 (1) ◽  
pp. 111-118 ◽  
Author(s):  
George M. Kleinman ◽  
William C. Schoene ◽  
Thomas M. Walshe ◽  
Edward P. Richardson

✓ The authors give follow-up information on Case 59 of Cushing's 1931 series of cerebellar astrocytomas. The patient died with a malignant cerebellar astrocytoma 48 years after partial removal of a previously benign astrocytoma at the same site. Including the present one, there have been only five reported cases in which this has occurred. Ordinarily, juvenile pilocytic astrocytomas are of extremely benign character, and it is well established that even with incomplete resections patients have survived for years without progression of the tumor. Not all of the cases so reported can be wholly accepted as representing malignant transformation of the tumor, but may instead be instances of recurrence of an inherently benign glioma since the presence of features such as endothelial hyperplasia or nuclear atypicality in a juvenile pilocytic astrocytoma does not warrant its being classified as malignant. Features truly suggestive of malignancy are hypercellularity, frequent mitoses, necrosis, and, in some instances, a diffusely infiltrative growth pattern; all of these features were found in the present case.


2011 ◽  
Vol 58 (5) ◽  
pp. 815-818 ◽  
Author(s):  
E. Anders Kolb ◽  
Richard Gorlick ◽  
Stephen T. Keir ◽  
John M. Maris ◽  
Richard Lock ◽  
...  

2011 ◽  
Vol 58 (4) ◽  
pp. 566-571 ◽  
Author(s):  
Christopher L. Morton ◽  
John M. Maris ◽  
Stephen T. Keir ◽  
Richard Gorlick ◽  
E. Anders Kolb ◽  
...  

2014 ◽  
Vol 61 (10) ◽  
pp. 1816-1821 ◽  
Author(s):  
E. Anders Kolb ◽  
Richard Gorlick ◽  
Catherine A. Billups ◽  
Thomas Hawthorne ◽  
Raushan T. Kurmasheva ◽  
...  

2015 ◽  
Vol 83 (7) ◽  
pp. 736-737 ◽  
Author(s):  
Sugata Narayan Biswas ◽  
Souvik Biswas ◽  
Partha Pratim Chakraborty

2010 ◽  
Vol 5 (2) ◽  
pp. 149-154 ◽  
Author(s):  
Andrew Jea ◽  
Ernesto Coscarella ◽  
Murali Chintagumpala ◽  
Meena Bhattacharjee ◽  
William E. Whitehead ◽  
...  

Multiple metastatic brain tumors and multifocal primary brain tumors of a single histological type have been published in the adult and pediatric literature. However, the simultaneous occurrence of multiple primary brain tumors with different cell types is rare. Even more rare is the pediatric presentation of multiple primary brain tumors with different cell types. The authors describe the case of an 8-year-old boy who presented with a 2-week history of progressive headache, nausea and vomiting, and imbalance. Brain MR imaging demonstrated a heterogeneously enhancing mixed solid/cystic mass of the left cerebellar hemisphere and a larger, midline, more homogeneously enhancing lesion of the superior vermis. Spinal MR imaging was unremarkable. The patient underwent a suboccipital craniotomy and subsequent gross-total resection of both mass lesions. Pathological examination revealed the left cerebellar and superior vermian lesions to be a juvenile pilocytic astrocytoma and a medulloblastoma, respectively. The patient did well in the immediate postoperative period, was discharged home, and underwent neurooncological follow-up. To the best of the authors' knowledge, they describe the first known pediatric case in which a medulloblastoma and a juvenile pilocytic astrocytoma presented as synchronous primary brain tumors. They review the literature on multiple primary brain tumors with different histological characteristics and rehash potential mechanisms for their development.


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