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1.
J Pediatr (Rio J) ; 88(1): 87-92, 2012.
Article in English | MEDLINE | ID: mdl-22344501

ABSTRACT

OBJECTIVE: To perform a comparative assessment of the clinical and epidemiological aspects of testicular tumors in childhood and adolescence. METHODS: Retrospective analysis of medical records of patients with testicular or paratesticular neoplasms. Patients under 10 years were classified as children and patients between 10 and 20 were classified as adolescents. The obtained results were compared through the two-sample test for proportions: non-parametric Mann-Whitney test and log-rank test. RESULTS: 60 patients were admitted in the period from January 1992 to July 2009: 34 children and 26 adolescents with testicular or paratesticular neoplasms. The main manifestations were testicular tumor and scrotal pain. Pain complaints were more common in adolescents (p = 0.006), who presented a mean time from disease onset to diagnosis of 4.9 months, longer than children, who presented a period of 2.3 months from disease onset to diagnosis (p = 0.01). Histological types were as follows: germ cell tumors in 32/60 (53%), rhabdomyosarcomas (RMSs) in 23/60 (38.3%), and other in 5/60 (8.3%). Adolescents presented a higher incidence of RMSs, lymph node metastases (p = 0.003) and distant metastases (p = 0.035). Differences in survival rates among the studied patients were not statistically significant, the only indicative being that survival in RMS cases is longer for children (p = 0.072). CONCLUSIONS: Compared to children, adolescents with testicular tumor presented longer time from disease onset to diagnosis, aggressive histological type and advanced illness at diagnosis, despite the small sample analyzed.


Subject(s)
Neoplasms, Germ Cell and Embryonal , Testicular Neoplasms , Acute Pain/etiology , Adolescent , Age Distribution , Brazil/epidemiology , Child , Epidemiologic Methods , Humans , Liver Neoplasms/secondary , Lung Neoplasms/secondary , Male , Neoplasms, Germ Cell and Embryonal/complications , Neoplasms, Germ Cell and Embryonal/epidemiology , Neoplasms, Germ Cell and Embryonal/pathology , Rhabdomyosarcoma/complications , Rhabdomyosarcoma/epidemiology , Rhabdomyosarcoma/pathology , Scrotum , Survival Rate , Testicular Neoplasms/complications , Testicular Neoplasms/epidemiology , Testicular Neoplasms/pathology , Time Factors , Young Adult
2.
J. pediatr. (Rio J.) ; J. pediatr. (Rio J.);88(1): 87-92, jan.-fev. 2012. ilus, graf
Article in Portuguese | LILACS | ID: lil-617055

ABSTRACT

OBJETIVO: Avaliar comparativamente aspectos clínicos e epidemiológicos dos tumores de testículo na infância e adolescência. MÉTODOS: Análise retrospectiva dos prontuários de pacientes com neoplasias de testículo ou paratesticulares. Foram classificados como crianças os menores de 10 anos e como adolescentes os pacientes entre 10 e 20 anos. Os resultados obtidos foram comparados por meio do teste para duas proporções: teste não paramétrico de Mann-Whitney e teste de log-rank. RESULTADOS: No período de janeiro de 1992 a julho de 2009, foram admitidos 60 pacientes: 34 crianças e 26 adolescentes com neoplasias de testículo ou paratesticulares. As principais manifestações foram tumor e dor na bolsa escrotal. A queixa de dor foi mais comum em adolescentes (p = 0,006). Estes apresentaram tempo médio de história de 4,9 meses, mais prolongado do que crianças, com 2,3 meses (p = 0,01). Os tipos histológicos encontrados foram: tumores de células germinativas em 32/60 (53 por cento), rabdomiossarcomas (RMSs) em 23/60 (38,3 por cento) e outros em 5/60 (8,3 por cento). Os adolescentes apresentaram maior frequência de RMSs, metástases em linfonodos (p = 0,003) e a distância (p = 0,035). As diferenças na sobrevida dos pacientes estudados não foram estatisticamente significantes, havendo apenas indicativo de que a sobrevida, nos casos de RMS, é maior nas crianças (p = 0,072). CONCLUSÕES: Os adolescentes com tumor testicular apresentaram maior tempo de história, tipo histológico agressivo e doença avançada ao diagnóstico quando comparados às crianças, a despeito da pequena amostra.


OBJECTIVE: To perform a comparative assessment of the clinical and epidemiological aspects of testicular tumors in childhood and adolescence. METHODS: Retrospective analysis of medical records of patients with testicular or paratesticular neoplasms. Patients under 10 years were classified as children and patients between 10 and 20 were classified as adolescents. The obtained results were compared through the two-sample test for proportions: non-parametric Mann-Whitney test and log-rank test. RESULTS: 60 patients were admitted in the period from January 1992 to July 2009: 34 children and 26 adolescents with testicular or paratesticular neoplasms. The main manifestations were testicular tumor and scrotal pain. Pain complaints were more common in adolescents (p = 0.006), who presented a mean time from disease onset to diagnosis of 4.9 months, longer than children, who presented a period of 2.3 months from disease onset to diagnosis (p = 0.01). Histological types were as follows: germ cell tumors in 32/60 (53 percent), rhabdomyosarcomas (RMSs) in 23/60 (38.3 percent), and other in 5/60 (8.3 percent). Adolescents presented a higher incidence of RMSs, lymph node metastases (p = 0.003) and distant metastases (p = 0.035). Differences in survival rates among the studied patients were not statistically significant, the only indicative being that survival in RMS cases is longer for children (p = 0.072). CONCLUSIONS: Compared to children, adolescents with testicular tumor presented longer time from disease onset to diagnosis, aggressive histological type and advanced illness at diagnosis, despite the small sample analyzed.


Subject(s)
Adolescent , Child , Humans , Male , Young Adult , Neoplasms, Germ Cell and Embryonal , Testicular Neoplasms , Age Distribution , Acute Pain/etiology , Brazil/epidemiology , Epidemiologic Methods , Liver Neoplasms/secondary , Lung Neoplasms/secondary , Neoplasms, Germ Cell and Embryonal/complications , Neoplasms, Germ Cell and Embryonal/epidemiology , Neoplasms, Germ Cell and Embryonal/pathology , Rhabdomyosarcoma/complications , Rhabdomyosarcoma/epidemiology , Rhabdomyosarcoma/pathology , Scrotum , Survival Rate , Time Factors , Testicular Neoplasms/complications , Testicular Neoplasms/epidemiology , Testicular Neoplasms/pathology
3.
J Clin Oncol ; 24(7): 1161-8, 2006 Mar 01.
Article in English | MEDLINE | ID: mdl-16505436

ABSTRACT

PURPOSE: To evaluate the impact of chemotherapy and surgery on the outcome of osteosarcoma (OS) of the extremities and to identify prognostic factors in Brazilian patients. PATIENTS AND METHODS: A total of 225 patients with metastatic and nonmetastatic OS of the extremities were enrolled and assessed in two consecutive studies designed and implemented by the Brazilian Osteosarcoma Treatment Group. RESULTS: The 5-year survival and event-free survival rates for the 209 assessable patients were 50.1% and 39%, respectively; for the 178 patients with nonmetastatic disease at diagnosis, the rates were 60.5% and 45.5%, respectively. The multivariate analysis showed that the following variables were associated with a shorter survival: metastases at diagnosis (P < .001), necrosis grades 1 and 2 (P = .046), and tumor size (P = .0071). CONCLUSION: The overall 5- and 10-year survival rates were lower than the rates reported in North American and European trials. A pattern of advanced disease at diagnosis was often present, with a high proportion of patients having metastases (20.8%) and large tumor size (42.9%). However, these features were not necessarily associated with longer duration of prediagnostic symptoms. These findings were considered in the strategic planning of the current Brazilian cooperative study, with the aim of improving survival and quality of life of a large number of patients with OS.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Bone Neoplasms/drug therapy , Bone Neoplasms/surgery , Orthopedic Procedures , Osteosarcoma/drug therapy , Osteosarcoma/surgery , Adolescent , Amputation, Surgical , Bone Neoplasms/pathology , Brazil , Carboplatin/administration & dosage , Chemotherapy, Adjuvant , Child , Cisplatin/administration & dosage , Disease-Free Survival , Doxorubicin/administration & dosage , Epirubicin/administration & dosage , Female , Humans , Ifosfamide/administration & dosage , Limb Salvage , Lung Neoplasms/drug therapy , Lung Neoplasms/secondary , Lung Neoplasms/surgery , Male , Methotrexate/administration & dosage , Multivariate Analysis , Orthopedic Procedures/methods , Osteosarcoma/secondary , Predictive Value of Tests , Prognosis , Proportional Hazards Models , Prospective Studies , Risk Factors , Survival Analysis , Treatment Outcome
4.
Rev. bras. cancerol ; 43(3): 191-203, jul.-set. 1997. tab, graf
Article in Portuguese | LILACS | ID: lil-199508

ABSTRACT

O câncer representa hoje a primeira causa de morte por doença entre a populaçÝo de faixa etária compreendida entre 1 e 21 anos nos Estados Unidos e em outros países economicamente desenvolvidos. No Brasil, esta doença figura como a terceira causa de morte por doença entre a populaçäo de faixa etária compreendida entre 1 e 14 anos, sendo já a primeira causa de óbito no município e no estado de Säo Paulo no grupo etário compreendido entre 5 e 14 anos, excluindo-se acidentes e causas externas. O objetivo deste artigo é informar a classe médica, principalmente a pediátrica, das particularidades do câncer infantil e de suas diferenças com as formas dos adultos, mais conhecidas e freqüentes. Graças à moderna abordagem multidisciplinar, o câncer infantil pode atingir índices de cura de 60 porcento a 70 porcento, mas, para tal, é imprescindível o diagnóstico precoce. Portanto, é importante que toda a comunidade pediátrica mostre-se motivada e informada sobre os sinais e sintomas das neoplasias pediátricas, já que näo dispomos de métodos de "screening" täo úteis e eficazes como para o controle do câncer do adulto.


Subject(s)
Humans , Infant , Child, Preschool , Child , Adolescent , Adult , Neoplasms/diagnosis , Neoplasms/epidemiology , Neoplasms/mortality , Neoplasms/prevention & control , Neoplasms/therapy , Oncogenes , Pediatrics , Survival Rate , Brazil , United States
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