Auszug
Weichteilsarkome sind seltene Tumoren im Kindesalter. Trotzdem stehen sie auf Rang 6 der häufigsten Kindertumoren. Ihre Behandlung erfolgt abhängig von unterschiedlichen Stadien, Ihrer Lokalisationen, der Histologie, des diffus infiltrierenden Wachstums und des Patientenalter, und stellt eine Herausforderung an die interdisziplinäre Zusammenarbeitzwischen Chirurg, Onkologe und Radiotherapeut dar.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
Literatur
Abbas AE, Deschamps C, Cassivi SD, Nichols FC 3rd, Allen MS, Schleck CD, Pairolero PC (2004) Chest wall desmoid tumors: results of surgical intervention. Ann Thorac Surg 78:1219–23
Buwalda J, Schouwenburg PF, Blank LE, Merks JH, Copper MP, Strackee SD, Voute PA, Caron HN (2003) A novel local treatment strategy for advanced stage head and neck rhabdomyosarcomas in children: results of the AMORE protocol. Eur J Cancer 39:1594–602
Crist W, Gehan EA, Ragab AH, Dickman PS, Donaldson SS, Fryer C, Hammond D, Hays DM, Herrmann J, Heyn R (1995) The third Intergroup Rhabdomyosarcoma Study. J Clin Oncol 13:610–630
Crist WM, Anderson JR, Meza JL, Fryer C, Raney RB, Ruymann FB, Breneman J, Qualman SJ, Wiener E, Wharam M, Lobe T, Webber B, Maurer HM, Donaldson SS (2001) Intergroup Rhabdomyosarcoma Study-IV: results for patients with nonmetastatic disease. J Clin Oncol 19:3091–3102
Donaldson SS, Anderson JR (2005) Rhabdomyosarcoma: many similarities, a few philosophical differences (editorial). J Clin Oncol 23:2586–2587
Ferrari A, Bisogno G, Casanova M, Meazza C, Piva L, Cecchetto G, Zanetti I, Pilz T, Mattke A, Treuner J, Carli M (2002) Paratesticular rhabdomyosarcoma: report from the Italian and the german Cooperative group. J Clin Oncol 20:449–455
Kohashi K, Oda Y, Yamamoto H, et al. (2007) Highly aggressive behavior of malignant rhabdoid tumor: a special reference to SMARCB1/INI1 gene alterations using molecular genetic analysis including realtime PCR. J Cancer Res Clin Oncol 133:817–824
LaQuaglia MP, Spiro SA, Ghavimi F, et al. (1993) Liposarcoma in patients younger than or equal to 22 years of age. Cancer 72:3114 [S10]
Magné N, Haie-Meder C (2007) Brachytherapy for genital-tract rhabdomyosarcomas in girls: technical aspects, reports, and perspectives. Lancet Oncol 8:725–9
McMulkin HM, Yanchar NL, Fernandez CV, Giacomantonio C (2003) Sentinel lymph node mapping and biopsy: a potentially viable tool in the management of of childhood extremity Rhabdomyosarcoma. Pediatr Surg Int 19:453–456
Miller GG, Yanchar NL, Magee JF, Blair GK (1998) Lipoblastoma and liposarcoma in children: an analysis of 9 cases and a review of the literature. Can J Surg 41:455–458
Newton WA, Gehan EA, Webber MD, Marsden HB, van Unnik AJM, Hamoudi AB, Tsokos MC, Shimada H, Harms D, Schmidt D, Ninfo V, Cavazzana AO, Gonzalez-Crussi F, Parham DM, Reiman HM, Asmar L, Beltangady MS, Sachs NE, Triche TJ, Maurer HM (1995) Classification of rhabdomyosarcoma and related sarcomas. Cancer 76:1073–85
Rao BN (1993) Nonrhabdomyosarcoma in children: Prognostic factors influencing survival. Semin Surg Oncol 9:524–531
Reinhard H, Reinert J, Beier R, et al. (2008) Rhabdoid tumors in children: prognostic factors in 70 patients diagnosed in Germany. Oncol Rep 19:819–823
Sonmelet-Olive D, Oberlin O, Flamant F, et al. (1995) Non-rhabdomyosarcoma malignamt mesenchymal tumors in children: results of SIOP MMT 84 and 89 protocols. Proc Am Soc Clin Ocol 14:446
Stevens MCG, Oberlin O, Rey A, Praquin MT, for the SIOP MMT Committee (1995) Non metastatic Rhabdomyosarcoma (RMS): Update from the SIOP MMT 89 study and implications for SIOP MMT 95. MPO 25:256 (abstract)
Stevens MCG, Rey A, Bouvet N, Ellershaw C, Flamant F, Habrand JL, Marsden HB, Martelli H, Sanchez de Toledo J, Spicer JD, Spooner D, Terrier-Lacombe MJ, van Unnik A, Oberlinet O (2005) Treatment of nonmetastatic rhabdomyosar coma in childhood and adolescence: Third study of the International Society of Paediatric Oncology — SIOP Malignant Mesenchymal Tumor 89. J Clin Oncol 23:2618–2628
Treuner J, Brecht I (2006) Weichteilsarkome. In: Gadner H, Gaedicke G, Niemeyer C, Ritter J (Hrsg.) Pädiatrische Hämatologie und Onkologie. Springer, Berlin Heidelberg New York, S. 865–881
Weiss SW (1994) Histological typing of soft tissue tumors, 2nd ed. Springer, Berlin Heidelberg New York
Willis RA (1992) The borderland of embryology and pathology, 2nd ed. Butterworths, London
Author information
Authors and Affiliations
Rights and permissions
Copyright information
© 2009 Springer Medizin Verlag Heidelberg
About this chapter
Cite this chapter
Aronson, D.C. (2009). Weichteiltumoren aller Lokalitäten. In: Kinderchirurgie. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-89032-4_47
Download citation
DOI: https://doi.org/10.1007/978-3-540-89032-4_47
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-540-89031-7
Online ISBN: 978-3-540-89032-4
eBook Packages: Medicine (German Language)