2018, Number 4
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Rev Clin Esc Med 2018; 8 (4)
Osteosarcoma: Etiología, diagnóstico y tratamiento
de Armas L, Delgado D, Alvarado K, Cordero C
Language: Spanish
References: 18
Page: 1-5
PDF size: 293.11 Kb.
ABSTRACT
Osteosarcoma is the most common primary bone
tumor (16), a spindle cell neoplasm that produces
osteoid matrix, ie non-mineralized bone (12). they
are aggressive tumors locally and tend to produce
metastases early; the most common histological type is
the conventional one presented in 75% of cases (4, 11).
there are two major peaks of incidence, the first one
affects children and adolescents in the second decade
of life, these are mostly sporadic And occur in the
metaphysis of long bones; the second peak occurs in
the fifth or sixth decade and tends to be secondary to
radiation or to the transformation of preexisting benign
processes as in bone Paget disease, having a preference
for axial locations. Survival of patients has improved
drastically with the correct use of chemotherapy, since
at the time of diagnosis subclinical metastases are very
likely.
REFERENCES
Ahrar K, Himmerich Judy et al. (2004). “Percutaneous Ultrasound-guided Biopsy in the Definitive Diagnosis of Osteosarcoma”. J Vasc Interv Radiol, 15(11): 1329-1333
Anderson M. (2016). “Update on Survival in Osteosrcoma”. Orthop Clin N Am, (47)1: 283-292.
Devita V, Lawrence T, Rosenberg S. “Devita, Hellman and Rosenberg´s Cancer Principles & Practice of Oncology”. 10th edition. Wolters Kluwer Health. USA .2015. pp 1292-1311
Durfee R, Mohammed M & Luu H. (2016). “Review of Osteosarcoma and Current Management”. Rheumatol Ther. 3(2):221-243 DOI: 10.1007/s40744- 016-0046-y
Ferrari S & Serta M. (2015). “An uptodate on chemotherapy for osteosarcoma”. Expert Opinion on Pharmacotehrapy. 16(18): 1-10 DOI: 10.1517/14656566.2015.110226
Friedrich P, Ortiz R, Strait K et al. (2012). “Pediatric Sarcoma in Centro America” Cancer 119(4): 871-879. DOI: 10.1002/cncr.27816
Gerrand C, Athanasou N et al. (2016). “UK guidelines for the management of bone sarcoma”. Clinical Sarcoma Research, (6)7. doi: 10.1186/ s13569-016-0047-1
Grimer R. (2005). “Surgical options for children with osteosarcoma”. Lancet Oncol, Vol 6: 85-92
Hayden J, Hoang B. (2006). “Osteosarcoma: Basic Science and Clinical Implications”. Ortop Clin N Am, (37)1; 1-7 DOI: 10.1016/j.ocl.2005.06.004
Hinds P, Gattuso J et al. (2009). “Aggressive treatmet of non-metastatic osteosarcoma improves health-related quality of the life in children and adolescents”. European Journal of Cancer, 45(11): 2007-2014
Luetke A, Meyers P, Lewis I & Juergens H. (2013). “Osteosarcoma treatment-Where do we stand? A state of the review”. Cancer Treatment Reviews 40(4): 523-532 http://dx.doi.org/10.1016/j. ctrv.2013.11.006
Longo D, Kasper D, Jameson J, Fauci A, Hauser S, Loscalzo J. “Harrison Principios de Medicina Interna”. 18ª edición. McGraw-Hill Interamericana. México, D.F. 2012. pag: 817-821
Mirabello L, Troisi R y Savage S. (2009). “International osteosarcoma incidence patterns in children and adolscents, middles ages and erderly persons”. Int J Cancer. 125(1):229-234 DOI: 10.1002/ ijc.24320
Muscolo L, Germán L. Farfalli, Luis Aponte Tinao y Miguel A. Ayerza, Actualización en osteosarcoma, Rev. Asoc. Argent. Ortop. Traumatol. vol.74 no.1 Ciudad Autónoma de Buenos Aires ene./ mar. 2009, D
Sartori P. (2012). “Signo Radiologico del “sol naciente”. Revista argentina de radiología, (76)4: 343- 344
Skeel R, Khlief S. “Manual de quimioterapia del cáncer”. 8va edición. Lippincott Williams & Wilkins. Barcelona, España. 2012. Pp 324-336.
Tabone MD, Rodary C, Oberlin O et al. (2005), “Quality of life of Patients Treated During Childhood for Bone Tumor: Assesment by the Child Health Questionnaire”. Pediatric Blood & Cancer, 45(2): 207- 211. DOI: 10.1002/pbc.20297
William S. Ferguson M.D. & Allen M. Goorin M.D. (2001) Current Treatment of Osteosarcoma, Cancer Investigation, 19:3, 292-315, DOI: 10.1081/ CNV-100102557