15 results on '"Cancer in children -- Diagnosis"'
Search Results
2. Risk of childhood cancers associated with residence in agriculturally intense areas in the United States
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Carozza, Susan E., Li, Bo, Elgethun, Kai, and Whitworth, Ryan
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Agricultural chemicals -- Complications and side effects ,Agricultural chemicals -- Environmental aspects ,Agricultural chemicals -- Research ,Agricultural laborers -- Health aspects ,Cancer in children -- Risk factors ,Cancer in children -- Diagnosis ,Cancer in children -- Research - Abstract
BACKGROUND: The potential for widespread exposure to agricultural pesticides through drift during application raises concerns about possible health effects to exposed children living in areas of high agricultural activity. OBJECTIVES: We evaluated whether residence in a county with greater agricultural activity was associated with risk of developing cancer in children < 15 years of age. METHODS: Incidence data for U.S. children 0-14 years of age diagnosed with cancer between 1995 and 2001 were provided by member registries of the North American Association of Central Cancer Registries. We determined percent cropland for each county using agricultural census data, and used the overall study distribution to classify agriculturally intense counties. We estimated odds ratios and 95% confidence intervals for all ages and 5-year age groups for total cancers and selected cancer sites using logistic regression. RESULTS: Our study results showed statistically significant increased risk estimates for many types of childhood cancers associated with residence at diagnosis in counties having a moderate to high level of agricultural activity, with a remarkably consistent dose-response effect seen for counties having [greater than or equal to] 60% of the total county acreage devoted to farming. Risk for different cancers varied by type of crop. CONCLUSIONS: Although interpretation is limited by the ecologic design, in this study we were able to evaluate rarer childhood cancers across a diverse agricultural topography. The findings of this exploratory study support a continued interest in the possible impact of long-term, low-level pesticide exposure in communities located in agriculturally intense areas. KEY WORDS: agricultural pesticides, childhood cancers, farming, pediatric cancers. Environ Health Perspect 116:559-565 (2008). doi:10.1289/ehp.9967 available via http://dx.doi.org/ [Online 10 January 2008], Increased incidence of certain cancers among farmers and workers employed in agricultural settings has been reported in a variety of epidemiologic studies, raising concerns about exposure to agricultural chemicals in [...]
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- 2008
3. Parental adjustment to childhood cancer: a replication study
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Gerhardt, Cynthia A., Gutzwiller, Joeanne, Huiet, Kristine A., Fischer, Stephanie, Noll, Robert B., and Vannatta, Kathryn
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Cancer in children -- Causes of ,Cancer in children -- Diagnosis ,Cancer in children -- Risk factors ,Cancer in children -- Care and treatment ,Cancer in children -- History ,Statistical hypothesis testing -- Usage - Abstract
Using procedures identical to a study published 10 years earlier, parents of 49 children with cancer (48 mothers, 33 fathers) and 49 healthy classmates (49 mothers, 29 fathers) completed measures [...]
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- 2007
4. Chronic health conditions in adult survivors of childhood cancer
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Oeffinger, Kevin C., Mertens, Ann C., Sklar, Charles A., Kawashima, Toana, Hudson, Melissa M., Meadows, Anna T., Friedman, Debra L., Marina, Neyssa, Hobbie, Wendy, Kadan-Lottick, Nina S., Schwartz, Cindy L., Leisenring, Wendy, and Robison, Leslie L.
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Cancer in children -- Risk factors ,Cancer in children -- Diagnosis ,Cancer in children -- Care and treatment ,Cancer survivors -- Health aspects - Abstract
A study was conducted to investigate the large and geographically diverse cohort that is followed in the childhood Cancer Survivor Study (CCSS), with the goal of determining the prevalence, incidence, and severity of chronic health conditions in adult survivors of childhood cancer, and to determine the risk of chronic conditions in the survivors, as compared with their siblings. The findings suggest that survivors of childhood cancer have a high rate of illness owing to chronic health conditions.
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- 2006
5. Screening and surveillance for second malignant neoplasms in adult survivors of childhood cancer: a report from the childhood cancer survivor study
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Nathan, Paul Craig, Ness, Kirsten Kimberlie, Mahoney, Martin Christopher, Li, Zhenghong, Hudson, Melissa Maria, Ford, Jennifer Sylene, Landier, Wendy, Stovall, Marilyn, Armstrong, Gregory Thomas, Henderson, Tara Olive, Robison, Leslie L., and Oeffinger, Kevin Charles
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Cancer in children -- Risk factors ,Cancer in children -- Development and progression ,Cancer in children -- Diagnosis ,Cancer in children -- Research ,Colonoscopy -- Usage ,Colonoscopy -- Health aspects ,Health - Abstract
Background: Survivors of childhood cancer may develop a second malignant neoplasm during adulthood and therefore require regular surveillance. Objective: To examine adherence to population cancer screening guidelines by survivors at average risk for a second malignant neoplasm and adherence to cancer surveillance guidelines by survivors at high risk for a second malignant neoplasm. Design: Retrospective cohort study. Setting: The Childhood Cancer Survivor Study (CCSS), a 26-center study of long-term survivors of childhood cancer that was diagnosed between 1970 and 1986. Patients: 4329 male and 4018 female survivors of childhood cancer who completed a CCSS questionnaire assessing screening and surveillance for new cases of cancer. Measurements: Patient-reported receipt and timing of mammography, Papanicolaou smear, colonoscopy, or skin examination was categorized as adherent to the U.S. Preventive Services Task Force guidelines for survivors at average risk for breast or cervical cancer or the Children's Oncology Group guidelines for survivors at high risk for breast, colorectal, or skin cancer as a result of cancer therapy. Results: In average-risk female survivors, 2743 of 3392 (80.9%) reported having a Papanicolaou smear within the recommended period, and 140 of 209 (67.0%) reported mammography within the recommended period. In high-risk survivors, rates of recommended mammography among women were only 241 of 522 (46.2%) and the rates of colonoscopy and complete skin examinations among both sexes were 91 of 794 (11.5%) and 1290 of 4850 (26.6%), respectively. Limitations: Data were self-reported. Participants in the CCSS are a selected group of survivors, and their adherence may not be representative of all survivors of childhood cancer. Conclusion: Female survivors at average risk for a second malignant neoplasm show reasonable rates of screening for cervical and breast cancer. However, surveillance for new cases of cancer is very low in survivors at the highest risk for colon, breast, or skin cancer, suggesting that survivors and their physicians need education about their risks and recommended surveillance. Primary Funding Source: The National Cancer Institute, National Institutes of Health, and the American Lebanese Syrian Associated Charities.
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- 2010
6. Subsequent neoplasms in 5-year survivors of childhood cancer: the childhood cancer survivor study
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Friedman, Debra L., Whitton, John, Leisenring, Wendy, Mertens, Ann C., Hammond, Sue, Stovall, Marilyn, Donaldson, Sarah S., Meadows, Anna T., Robison, Leslie L., and Neglia, Joseph P.
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Cancer in children -- Risk factors ,Cancer in children -- Diagnosis ,Cancer in children -- Care and treatment ,Cancer in children -- Patient outcomes ,Cancer in children -- Research ,Radiotherapy -- Health aspects ,Radiotherapy -- Patient outcomes ,Health - Abstract
Background The occurrence of subsequent neoplasms has direct impact on the quantity and quality of life in cancer survivors. We have expanded our analysis of these events in the Childhood Cancer Survivor Study (CCSS) to better understand the occurrence of these events as the survivor population ages. Methods The incidence of and risk for subsequent neoplasms occurring 5 years or more after the childhood cancer diagnosis were determined among 14359 5-year survivors in the CCSS who were treated from 1970 through 1986 and who were at a median age of 30 years (range = 5-56 years) for this analysis. At 30 years after childhood cancer diagnosis, we calculated cumulative incidence at 30 years of subsequent neoplasms and calculated standardized incidence ratios (SIRs), excess absolute risks (EARs) for invasive second malignant neoplasms, and relative risks for subsequent neoplasms by use of multivariable Poisson regression. Results Among 14359 5-year survivors, 1402 subsequently developed 2703 neoplasms. Cumulative incidence at 30 years after the childhood cancer diagnosis was 20.5% (95% confidence interval [CI] = 19.1% to 21.8%) for all subsequent neoplasms, 7.9% (95% CI = 7.2% to 8.5%) for second malignant neoplasms (excluding nonmelanoma skin cancer), 9.1% (95% CI = 8.1% to 10.1%) for nonmelanoma skin cancer, and 3.1% (95% CI = 2.5% to 3.8%) for meningioma. Excess risk was evident for all primary diagnoses (EAR = 2.6 per 1000 person-years, 95% CI = 2.4 to 2.9 per 1000 person-years; SIR = 6.0, 95% CI = 5.5 to 6.4), with the highest being for Hodgkin lymphoma (SIR = 8.7, 95% CI = 7.7 to 9.8) and Ewing sarcoma (SIR = 8.5, 95% CI = 6.2 to 11.7). In the Poisson multivariable analysis, female sex, older age at diagnosis, earlier treatment era, diagnosis of Hodgkin lymphoma, and treatment with radiation therapy were associated with increased risk of subsequent neoplasm. Conclusions As childhood cancer survivors progress through adulthood, risk of subsequent neoplasms increases. Patients surviving Hodgkin lymphoma are at greatest risk. There is no evidence of risk reduction with increasing duration of follow-up. J Natl Cancer Inst 2010;102:1083-1095 DOI: 10.1093/jnci/djq238
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- 2010
7. Secondary sarcomas in childhood cancer survivors: a report from the childhood cancer survivor study
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Henderson, Tara O., Whitton, John, Stovall, Marilyn, Mertens, Ann C., Mitby, Pauline, Friedman, Debra, Strong, Louise C., Hammond, Sue, Neglia, Joseph P., Meadows, Anna T., Robison, Leslie, and Diller, Lisa
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Sarcoma -- Risk factors ,Sarcoma -- Diagnosis ,Sarcoma -- Care and treatment ,Cancer survivors -- Health aspects ,Cancer in children -- Risk factors ,Cancer in children -- Diagnosis ,Cancer in children -- Care and treatment ,Health - Abstract
Background Childhood cancer survivors are at increased risk for the development of secondary sarcomas. Exposure to radiation therapy is a known risk factor for the development of these sarcomas. Other risk factors for secondary sarcomas have not been well described for childhood cancer survivors. We analyzed a large cohort of childhood cancer survivors to determine the true incidence of secondary sarcomas and to examine factors associated with the risk of developing secondary sarcomas. Methods The history of secondary sarcomas in 14372 participants in the Childhood Cancer Survivor Study was determined from self-reports in three questionnaires. Risk of secondary sarcoma was evaluated by use of standardized incidence ratios (SIRs) and excess absolute risks (EARs) as calculated by use of data from the Surveillance, Epidemiology, and End Results Program. Cox regression models were used to estimate hazard ratios of developing subsequent sarcomas. Hazard ratios were reported as relative risks (RRs). Results We identified 108 patients with sarcomas that were diagnosed a median of 11 years after the diagnosis of childhood cancer. The risk of sarcoma was more than ninefold higher among childhood cancer survivors than among the general population (SIR = 9.02, 95% confidence interval [CI] = 7.44 to 10.93). The excess absolute risk of secondary sarcoma was 32.5 per 100000 person-years (95% CI = 26.1 to 40.3 per 100000 person-years). Higher standardized incidence ratios and excess absolute risks were associated with young age at primary diagnosis, primary sarcoma diagnosis, and a family history of cancer. In a multivariable model, increased risk of secondary sarcoma was associated with radiation therapy (RR = 3.1, 95% CI = 1.5 to 6.2), with a primary diagnosis of sarcoma (RR = 10.1, 95% CI = 4.7 to 21.8), with a history of other secondary neoplasms (RR = 2.2, 95% CI = 1.1 to 4.5), and with treatment with higher doses of anthracyclines (RR = 2.3, 95% CI = 1.2 to 4.3) or alkylating agents (RR = 2.2, 95% CI = 1.1 to 4.6). Conclusion Childhood cancer survivors appear to be at increased risk for secondary sarcomas compared with general population rates.
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- 2007
8. Epidemiology of childhood cancer in India
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Arora, R., Eden, Tob, and Kapoor, G.
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Cancer in children -- Care and treatment ,Cancer in children -- Risk factors ,Cancer in children -- Diagnosis ,Cancer in children -- Research ,Epidemiology -- Research - Abstract
Byline: R. Arora, TOB. Eden, G. Kapoor There has been enormous progress in the treatment of childhood cancer in the developed world and the epidemiology in these countries is well [...]
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- 2009
9. Childhood cancers in India: Burden, barriers, and breakthroughs
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Arora, B. and Kanwar, V.
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Cancer in children -- Risk factors ,Cancer in children -- Diagnosis ,Cancer in children -- Care and treatment ,Cancer in children -- Research ,Medical personnel -- Practice ,Medical personnel -- Services ,Cancer -- Diagnosis ,Cancer -- Health aspects - Abstract
Byline: B. Arora, V. Kanwar Childhood cancer contributes to less than 5% of the total cancer burden in India, with approximately 45,000 children diagnosed with cancer every year. In the [...]
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- 2009
10. Proceedings of the consensus meetings from the International Retinoblastoma Staging Working Group on the pathology guidelines for the examination of enucleated eyes and evaluation of prognostic risk factors in retinoblastoma
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Sastre, Xavier, Chantada, Guillermo L., Doz, Francois, Wilson, Matthew W., de Davila, Maria T.G., Rodriguez-Galindo, Carlos, Chintagumpala, Murali, and Chevez-Barrios, Patricia
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Retinoblastoma -- Risk factors ,Retinoblastoma -- Diagnosis ,Retinoblastoma -- Care and treatment ,Cancer in children -- Diagnosis ,Cancer in children -- Risk factors ,Cancer in children -- Care and treatment ,Histology, Pathological -- Research ,Clinical pathology -- Research - Abstract
* Retinoblastoma is the most common intraocular malignant childhood tumor in need of prospective clinical trials to address important unanswered questions about biology, treatment, and prognostic factors. Currently, there is controversy about the definitions for choroidal invasion and an inconsistency in the handling of eyes with retinoblastoma. The International Retinoblastoma Staging Working Group (IRSWG) composed of 58 participants from 24 countries on 4 continents had a series of Internet meetings to discuss the staging and tissue handling guidelines to reach consensus for adequate processing, establishing definitions of histopathologic risk factors, and reporting of enucleated eyes with retinoblastoma to serve as the basis for clinical trials and studies to validate the proposed criteria. The meetings were facilitated by the International Outreach Program of the St. Jude Children's Research Hospital through Cure4Kids. The retinoblastoma guidelines from the Children's Oncology Group, the French Society for Pediatric Cancers, the Association of Directors of Anatomic and Surgical Pathology, and some published data were the basis for this consensus document. Discussions of the feasibility, practicality, and efficacy of the guidelines and criteria resulted in this report. The consensus definitions reached included definition of massive choroidal invasion stated as a maximum diameter of invasive tumor focus of 3 mm or more that may reach the scleral tissue. Focal choroidal invasion is defined as a tumor focus of less than 3 mm and not reaching the sclera. Optic nerve invasion is classified as prelaminar, laminar, retrolaminar, or tumor at surgical margin, and the measurement of the depth of invasion should also be recorded. These guidelines also address handling of the enucleated eye with retinoblastoma in an efficient, practical, and feasible manner for a meaningful diagnosis. The consensus criteria reached by the IRSWG should be validated through prospective clinical trials and studies. (Arch Pathol Lab Med. 2009;133:1199-1202), Retinoblastoma--the most frequent primary intraocular tumor in children--lacks validation of a number of prognostic factors and requires a consensus on criteria for processing and interpreting histopathologic features. This is unlike [...]
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- 2009
11. Pediatric carcinoma of rectum - Varanasi experience
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Pandey, A., Gangopadhyay, A., Sharma, S., Kumar, V., Gupta, D., Gopal, S., and Singh, R.
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Colorectal cancer -- Diagnosis ,Colorectal cancer -- Risk factors ,Colorectal cancer -- Care and treatment ,Colorectal cancer -- Prognosis ,Cancer in children -- Risk factors ,Cancer in children -- Diagnosis ,Cancer in children -- Care and treatment ,Cancer in children -- Prognosis - Abstract
Byline: A. Pandey, A. Gangopadhyay, S. Sharma, V. Kumar, D. Gupta, S. Gopal, R. Singh Background : Primary gastrointestinal system malignancies constitute approximately 2% of pediatric neoplasm and of these; [...]
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- 2008
12. Pediatric pituitary adenomas
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Webb, Christopher and Prayson, Richard A.
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Cancer in children -- Statistics ,Cancer in children -- Patient outcomes ,Cancer in children -- Risk factors ,Cancer in children -- Diagnosis ,Pituitary gland tumors -- Statistics ,Pituitary gland tumors -- Patient outcomes ,Pituitary gland tumors -- Risk factors ,Pituitary gland tumors -- Diagnosis - Abstract
Context.--Pituitary adenomas are relatively rare occurrences in the pediatric population, and there are few studies documenting the profile of these tumors in this age group. Objective.--To study the clinical and pathologic features of pediatric pituitary adenomas in conjunction with a review of the available literature. Design.--A retrospective clinicopathologic review of 20 pediatric patients (younger than 20 years of age) with pituitary adenomas resected during a 24.5-year period (1981-2005). Results.--A total of 20 patients, including 12 females and 8 males, comprise the study group. Mean age at onset of symptoms was 14.0 years (range, 5-18 years). Four patients had onset of symptoms before the age of 12 years. The majority of patients presented with headaches (n = 12), visual disturbances (n = 12) or, in females, menstrual dysfunction (n = 9/12). Tumor size based on radiographic data was known for 19 tumors; 12 adenomas were greater than 1 cm in greatest dimension, and 7 were less than 1 cm. On follow-up, 2 patients with total gross tumor resections had recurrent adenomas; time to recurrence was 5 months and 17 months, respectively. Nine adenomas stained solely for prolactin, 5 for adrenocorticotropic hormone, and 3 for growth hormone. Two stained for growth hormone and prolactin. One did not stain with hormone antibodies. Conclusions.--Most pediatric pituitary adenomas present after the onset of puberty and present with frequent headaches, changes in visual acuity and, in females, menstrual dysfunction. Most (19/20) were secretory, with prolactinomas being the most common type., Pituitary adenomas in children are relatively infrequent occurrences. (1-8) Most studies report the incidence of these tumors to be between 1% and 10% of all childhood brain tumors (9-12) and [...]
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- 2008
13. Monitor kids for malignant melanomas
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Little, Linda
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Cancer in children -- Risk factors ,Cancer in children -- Diagnosis ,Cancer in children -- Care and treatment ,Sun exposure -- Health aspects ,Melanoma -- Risk factors ,Melanoma -- Diagnosis ,Melanoma -- Care and treatment ,Health ,Health care industry - Abstract
SCOTTSDALE, ARIZ. -- Although childhood malignant melanomas are rare, physicians must keep an eye out for them, Ronald C. Hansen, M.D., said at a pediatric update sponsored by Phoenix Children's [...]
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- 2005
14. Pulse Clinical:How not to miss childhood cancer
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Cancer in children -- Causes of ,Cancer in children -- Diagnosis ,Cancer in children -- Risk factors ,Health ,Health care industry - Abstract
Dr Bruce Morland advises on key signs to look for Worst outcomes if missed * Death * More advanced disease when eventually diagnosed (eg presence of metastatic disease) resulting in [...]
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- 2006
15. Pediatric Cancer Emergencies: Critical Diagnostic and Management Strategies
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Chemotherapy -- Health aspects ,Chemotherapy -- Analysis ,Emergency medicine -- Health aspects ,Cancer in children -- Risk factors ,Cancer in children -- Diagnosis ,Cancer in children -- Care and treatment ,Cancer in children -- Prognosis ,Cancer -- Chemotherapy ,Cancer -- Health aspects ,Cancer -- Analysis ,Family and marriage ,Health - Abstract
Pediatric Cancer Emergencies: Critical Diagnostic and Management Strategies Authors: Emily Fontane, MD, FACEP, FAAP, Assistant Clinical Professor of Emergency Medicine and Pediatrics, Brody School of Medicine at East Carolina University; [...]
- Published
- 2006
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