PortalPublikationenAtypical teratoid/rhabdoid tumor arising in a malignant glio...

Atypical teratoid/rhabdoid tumor arising in a malignant glioma

Standard

Atypical teratoid/rhabdoid tumor arising in a malignant glioma. / Bozzai, Barbara; Hasselblatt, Martin; Turányi, Eszter; Frühwald, Michael C; Siebert, Reiner; Bens, Susanne; Schneppenheim, Reinhard; Kool, Marcel; Stelczer, Gábor; Hortobágyi, Tibor; Hauser, Peter.

in: PEDIATR BLOOD CANCER, Jahrgang 64, Nr. 1, 01.2017, S. 96-99.

Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung

Harvard

Bozzai, B, Hasselblatt, M, Turányi, E, Frühwald, MC, Siebert, R, Bens, S, Schneppenheim, R, Kool, M, Stelczer, G, Hortobágyi, T & Hauser, P 2017, 'Atypical teratoid/rhabdoid tumor arising in a malignant glioma', PEDIATR BLOOD CANCER, Jg. 64, Nr. 1, S. 96-99. https://doi.org/10.1002/pbc.26173

APA

Bozzai, B., Hasselblatt, M., Turányi, E., Frühwald, M. C., Siebert, R., Bens, S., Schneppenheim, R., Kool, M., Stelczer, G., Hortobágyi, T., & Hauser, P. (2017). Atypical teratoid/rhabdoid tumor arising in a malignant glioma. PEDIATR BLOOD CANCER, 64(1), 96-99. https://doi.org/10.1002/pbc.26173

Vancouver

Bozzai B, Hasselblatt M, Turányi E, Frühwald MC, Siebert R, Bens S et al. Atypical teratoid/rhabdoid tumor arising in a malignant glioma. PEDIATR BLOOD CANCER. 2017 Jan;64(1):96-99. https://doi.org/10.1002/pbc.26173

Bibtex

@article{cf545dcf34f34ac8ad659560ea6844d2,
title = "Atypical teratoid/rhabdoid tumor arising in a malignant glioma",
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.",
keywords = "Child, Preschool, Combined Modality Therapy, Female, Glioma, Humans, Neoplasm Recurrence, Local, Neoplasm Staging, Neoplasms, Second Primary, Prognosis, Rhabdoid Tumor, Teratoma, Case Reports, Journal Article",
author = "Barbara Bozzai and Martin Hasselblatt and Eszter Tur{\'a}nyi and Fr{\"u}hwald, {Michael C} and Reiner Siebert and Susanne Bens and Reinhard Schneppenheim and Marcel Kool and G{\'a}bor Stelczer and Tibor Hortob{\'a}gyi and Peter Hauser",
note = "{\textcopyright} 2016 Wiley Periodicals, Inc.",
year = "2017",
month = jan,
doi = "10.1002/pbc.26173",
language = "English",
volume = "64",
pages = "96--99",
journal = "PEDIATR BLOOD CANCER",
issn = "1545-5009",
publisher = "Wiley-Liss Inc.",
number = "1",

}

RIS

TY - JOUR

T1 - Atypical teratoid/rhabdoid tumor arising in a malignant glioma

AU - Bozzai, Barbara

AU - Hasselblatt, Martin

AU - Turányi, Eszter

AU - Frühwald, Michael C

AU - Siebert, Reiner

AU - Bens, Susanne

AU - Schneppenheim, Reinhard

AU - Kool, Marcel

AU - Stelczer, Gábor

AU - Hortobágyi, Tibor

AU - Hauser, Peter

N1 - © 2016 Wiley Periodicals, Inc.

PY - 2017/1

Y1 - 2017/1

N2 - 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.

AB - 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.

KW - Child, Preschool

KW - Combined Modality Therapy

KW - Female

KW - Glioma

KW - Humans

KW - Neoplasm Recurrence, Local

KW - Neoplasm Staging

KW - Neoplasms, Second Primary

KW - Prognosis

KW - Rhabdoid Tumor

KW - Teratoma

KW - Case Reports

KW - Journal Article

U2 - 10.1002/pbc.26173

DO - 10.1002/pbc.26173

M3 - SCORING: Journal article

C2 - 27472468

VL - 64

SP - 96

EP - 99

JO - PEDIATR BLOOD CANCER

JF - PEDIATR BLOOD CANCER

SN - 1545-5009

IS - 1

ER -