Solid Tumors of Childhood

作者: Crawford J. Strunk , Sarah W. Alexander

DOI: 10.1007/0-387-31056-8_62

关键词:

摘要: Cancer in children, as compared with adults, is rare. From 1993 to 2000, the incidence of cancer children and adolescents aged 0 19 years was approximately 160 cases per 1 million.1 Despite relative rarity disease progress made therapy, remains leading cause disease-related death ages years2 (Figure 62.1).

参考文章(284)
Holcombe E. Grier, The Ewing family of tumors. Ewing's sarcoma and primitive neuroectodermal tumors Pediatric Clinics of North America. ,vol. 44, pp. 991- 1004 ,(1997) , 10.1016/S0031-3955(05)70541-1
D. N. Shapiro, In-Sang Jeon, J. E. Sublett, The alveolar rhabdomyosarcoma PAX3/FKHR fusion protein is a transcriptional activator. Oncogene. ,vol. 11, pp. 545- 552 ,(1995)
Garrett M. Brodeur, Akira Nakagawara, Darrell J. Yamashiro, Naohiko Ikegaki, Xing-Ge Liu, Christopher G. Azar, Catherine P. Lee, Audrey E. Evans, Expression of TrkA, TrkB and TrkC in human neuroblastomas Journal of Neuro-oncology. ,vol. 31, pp. 49- 55 ,(1997) , 10.1023/A:1005729329526
Lutz Löning, Martin Zimmermann, Alfred Reiter, Peter Kaatsch, Günter Henze, Hansjörg Riehm, Martin Schrappe, Secondary neoplasms subsequent to Berlin-Frankfurt-Münster therapy of acute lymphoblastic leukemia in childhood: significantly lower risk without cranial radiotherapy. Blood. ,vol. 95, pp. 2770- 2775 ,(2000) , 10.1182/BLOOD.V95.9.2770.009K16_2770_2775
Junya Toguchida, Takao Yamamuro, Kanji Ishizaki, Masao S. Sasaki, Yoshihiko Kotoura, Yusuke Nakamura, Norihiko Takada, Noriyoshi Kawaguchi, Yasuhiko Kaneko, Toshikazu Yamaguchi, Allelotype analysis in osteosarcomas: frequent allele loss on 3q, 13q, 17p, and 18q. Cancer Research. ,vol. 52, pp. 2419- 2423 ,(1992)
Perry E. Telzerow, Vicki Huff, Paul E. Grundy, Jamie Moksness, Malcolm C. Paterson, Norman Breslow, Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome Cancer Research. ,vol. 54, pp. 2331- 2333 ,(1994)
Gail E. Tomlinson, Perry D. Nisen, Charles F. Timmons, Nancy R. Schneider, Cytogenetics of a renal cell carcinoma in a 17-month-old child. Evidence for Xp11.2 as a recurring breakpoint. Cancer Genetics and Cytogenetics. ,vol. 57, pp. 11- 17 ,(1991) , 10.1016/0165-4608(91)90184-V
Jörg Fuchs, Jana Rydzynski, Dietrich Von Schweinitz, Udo Bode, Hartmut Hecker, Peter Weinel, Dietrich Bürger, Dieter Harms, Rudolf Erttmann, Karl Oldhafer, Hermann Mildenberger, , Pretreatment prognostic factors and treatment results in children with hepatoblastoma: a report from the German Cooperative Pediatric Liver Tumor Study HB 94. Cancer. ,vol. 95, pp. 172- 182 ,(2002) , 10.1002/CNCR.10632
Tadashi Matsunaga, Fumiaki Sasaki, Mutsuro Ohira, Kohei Hashizume, Akira Hayashi, Yutaka Hayashi, Hideo Mugishima, Naomi Ohnuma, Analysis of treatment outcome for children with recurrent or metastatic hepatoblastoma Pediatric Surgery International. ,vol. 19, pp. 142- 146 ,(2003) , 10.1007/S00383-002-0906-0
M Tarkkanen, R Karhu, A Kallioniemi, Inkeri Elomaa, Aarne H Kivioja, Juha Nevalainen, T Böhling, E Karaharju, Eija Hyytinen, S Knuutila, Olli-P Kallioniemi, Gains and losses of DNA sequences in osteosarcomas by comparative genomic hybridization Cancer Research. ,vol. 55, pp. 1334- 1338 ,(1995)