dc.contributor.author |
Bozzai, Barbara |
|
dc.contributor.author |
Hasselblatt M |
|
dc.contributor.author |
Turányi, Eszter |
|
dc.contributor.author |
Fruhwald MC |
|
dc.contributor.author |
Siebert R |
|
dc.contributor.author |
Bens S |
|
dc.contributor.author |
Schneppenheim R |
|
dc.contributor.author |
Kool M |
|
dc.contributor.author |
Stelczer G |
|
dc.contributor.author |
Hortobagyi T |
|
dc.contributor.author |
Hauser, Péter |
|
dc.date.accessioned |
2017-03-27T11:33:11Z |
|
dc.date.available |
2017-03-27T11:33:11Z |
|
dc.date.issued |
2017 |
|
dc.identifier.citation |
pagination=96-99;
journalVolume=64;
journalIssueNumber=1;
journalTitle=PEDIATRIC BLOOD & CANCER; |
|
dc.identifier.uri |
http://repo.lib.semmelweis.hu//handle/123456789/4057 |
|
dc.identifier.uri |
doi:10.1002/pbc.26173 |
|
dc.description.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. |
|
dc.relation.ispartof |
urn:issn:1545-5009 |
|
dc.title |
Atypical teratoid/rhabdoid tumor arising in a malignant glioma |
|
dc.type |
Journal Article |
|
dc.date.updated |
2017-02-01T13:13:27Z |
|
dc.language.rfc3066 |
en |
|
dc.identifier.mtmt |
3104826 |
|
dc.identifier.pubmed |
27472468 |
|
dc.contributor.department |
SE/AOK/K/II. Sz. Gyermekgyógyászati Klinika |
|
dc.contributor.department |
SE/AOK/I/I. Sz. Patológiai és Kísérleti Rákkutató Intézet |
|
dc.contributor.institution |
Semmelweis Egyetem |
|