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@ARTICLE{Bozzai:119223,
author = {B. Bozzai and M. Hasselblatt and E. Turányi and M. C.
Frühwald and R. Siebert and S. Bens and R. Schneppenheim
and M. Kool$^*$ and G. Stelczer and T. Hortobágyi and P.
Hauser},
title = {{A}typical teratoid/rhabdoid tumor arising in a malignant
glioma.2},
journal = {Pediatric blood $\&$ cancer},
volume = {64},
number = {1},
issn = {1545-5009},
address = {New York, NY},
publisher = {Wiley},
reportid = {DKFZ-2017-00013},
pages = {96 - 99},
year = {2017},
abstract = {Atypical teratoid/rhabdoid tumor (AT/RT), a highly
malignant brain tumor in young children, usually arises de
novo and has only rarely been described as a secondary
malignancy. Here, we present a case of a child with
glioblastoma, who was treated postoperatively by a
combination of temozolomide, irradiation, and bevacizumab.
AT/RT was diagnosed as a secondary tumor, 2.5 years
following primary diagnosis. The child died 13 months after
the diagnosis of AT/RT. This case demonstrates that
malignant gliomas may give rise to AT/RT. It also emphasizes
the diagnostic value of a repeated tumor biopsy in the
recurrence setting.},
cin = {B062 / L101},
ddc = {610},
cid = {I:(DE-He78)B062-20160331 / I:(DE-He78)L101-20160331},
pnm = {312 - Functional and structural genomics (POF3-312)},
pid = {G:(DE-HGF)POF3-312},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:27472468},
doi = {10.1002/pbc.26173},
url = {https://inrepo02.dkfz.de/record/119223},
}