2011
DOI: 10.1007/s00132-011-1866-7
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Primär maligne Knochentumoren

Abstract: Among human neoplasms, primary malignant bone tumors are fairly rare. They present an incidence rate of roughly 10 cases per 1 million inhabitants per year. During childhood (<15 years), the percentage of malignant bone tumors amounts to 6% of all infantile malignancies. Only leukemia and lymphoma show a higher incidence in adolescence. Of all primary malignant bone tumors, 60% affect patients younger than 45 years and the peak incidence of all bone tumors occurs between 15 and 19 years. The most common primar… Show more

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Cited by 40 publications
(15 citation statements)
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“…Sarcomas account for approximately 1 % of all adult cancers [ 1 ]. In this context soft tissue sarcomas typically occur in middle aged and older adults [ 1 ], whereas malignant bone tumors, i.e., osteosarcoma and Ewing’s sarcoma are more frequent in children and adolescents [ 2 , 3 ]. Progress in modern treatment regimens including neoadjuvant and adjuvant therapy has markedly improved the overall survival rates over the last decades [ 4 ].…”
Section: Introductionmentioning
confidence: 99%
“…Sarcomas account for approximately 1 % of all adult cancers [ 1 ]. In this context soft tissue sarcomas typically occur in middle aged and older adults [ 1 ], whereas malignant bone tumors, i.e., osteosarcoma and Ewing’s sarcoma are more frequent in children and adolescents [ 2 , 3 ]. Progress in modern treatment regimens including neoadjuvant and adjuvant therapy has markedly improved the overall survival rates over the last decades [ 4 ].…”
Section: Introductionmentioning
confidence: 99%
“…Since primary spinal sarcomas are very rare diseases24,25), the standard treatment method has not been established28,34,38,39). However, treatment for osteosarcoma and chondrosarcoma is being conducted in uniform fashion.…”
Section: Discussionmentioning
confidence: 99%
“…Unter den Knochentumoren wird der Anteil von gutartigen Neoplasien mit etwa 40-50 % angegeben, wobei aufgrund der hohen Dunkelziffer (symptomlose Tumoren, welche dauerhaft unentdeckt bleiben, Zufallsbefunde etc.) und tumorähnlichen Läsionen deren Anteil als deutlich höher einzuschätzen ist [1,2].…”
Section: Grundlagen Und Epidemiologieunclassified
“…Die Prognose des Osteo-sowie des Ewing-Sarkoms konnte durch die Einführung der neo-/adjuvanten Chemotherapie deutlich verbessert werden, das 5-Jahres-Überleben liegt heute für beide Entitäten bei etwa 70 %. Die Prognose wird hierbei maßgeblich durch Faktoren beeinflusst [2] wie ▪ Tumorlokalisation, -größe und -volumen, ▪ das histologische Ansprechen auf Chemotherapie, ▪ das Vorliegen und die Art (pulmonal versus ossär) von Metastasen sowie ▪ die Art des Fusionstranskripts (bei Ewing-Sarkomen).…”
Section: Maligne Knochentumorenunclassified