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Osteologie 2019; 28(03): 231-233
DOI: 10.1055/a-0985-5046
DOI: 10.1055/a-0985-5046
Gesellschaftsnachrichten
Informationen der Arbeitsgemeinschaft Knochentumoren e.
V.
Pediatric bone tumors in Croatia, a single oncology centre experience
Further Information
Publication History
Publication Date:
12 September 2019 (online)
Introduction
Malignant bone tumors are recognized as rare diseases following the already estimated incidence which is well known, with osteosarcoma as the most common bone tumor [1], [2]. Median incidence rate for malignant childhood tumors in Croatia is 163 new cases during period 1987–2014, age 0–19 according to Croatian National Cancer Registry (CNCR) data ([ Fig. 1 ]).
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References
- 1 Mirabello L, Troisi RJ, Savage SA. Osteosarcoma Incidence and Survival Rates From 1973–2004: data from SEER. Cancer 2009; 1531-1543
- 2 Esiashvili N, Goodman M, Marcus Jr RB. Changes in incidence and survival of Ewing sarcoma patients over the past 3 decades: SEER data. J Pediatr Hematol Oncol 2008; 30 (06) 425-430
- 3 Bernstein M, Kovar H, Paulussen M. et al. Ewing sarcoma family of tumors: Ewing sarcoma of bone and soft tissue and the peripheral primitive neuroectodermal tumors. In: Pizzo P, Poplack D. eds. Principles and Practice of Pediatric Oncology. 5th ed.. Philadelphia, PA: Lippincott Wiliams and Wilkins; 2005: 1002-1032