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1.
J Neurooncol ; 132(3): 427-432, 2017 05.
Artículo en Inglés | MEDLINE | ID: mdl-28290001

RESUMEN

Choroid plexus tumors (CPT) are rare neoplasms accounting for 1-4% of all pediatric brain tumors. They are divided into choroid plexus papilloma (CPP), atypical choroid plexus papilloma (APP) and choroid plexus carcinoma (CPC). CPTs are known to primarily affect children less than 2 years of age. Gross total resection is the most important predictor of survival especially in CPC. Although small case series have been published, limited clinical data are available to describe treatment and outcome of CPTs. More clinical data would be necessary to complete the picture, particularly in populations that are not age limited. Here we share data from the two major hospitals in Cleveland to describe treatment and outcome of adult and pediatric patients. We performed a retrospective analysis of patients with CPT seen in Cleveland Clinic from 1990 to 2015 and at University Hospitals from 1994 to 2015. Results were compared to previously published historical controls. We identified 30 cases with CPT, including 22 pediatric and eight adult cases; 11 females and 19 males. The mean age at presentation was 12.4 years with a median age of 4.5 years (range 2 months-51 years). Gross total surgical resection was achieved in 22, subtotal resection in four, partial resection in two and unknown in two. The histology was CPP in 23 patients, two of whom developed recurrence requiring repeat resection and adjuvant therapy. Median event free survival (EFS) for CPP patients was 7.6 years. The histology was CPC in seven patients. All CPC patients were treated with adjuvant therapy. Median EFS of CPC patients was 4.4 years. Overall survival of all CPT patients was 100% with a median follow up of 7 years. A systematic literature review identified 1012 CPT patients treated from 1989 to 2013. The mean and median age of CPT patients was 13 and 3 years respectively. The median survival of 541 CPP patients was undefined vs. 2.7 years for the 452 CPC patients. The difference between the two populations was highly significant (p < 0.001). Kaplan-Meier survival curves comparing CPTs at Cleveland Clinic and University Hospitals versus a systematic literature review showed a statistically significant advancement in overall survival among the patients treated at Cleveland Clinic and University Hospitals. Our data are consistent with the literature review regarding epidemiology, clinical presentation, and treatment modalities but differed in regards to survival. Differences in survival may be related to different methods of data collection or details in patient care.


Asunto(s)
Carcinoma/patología , Carcinoma/terapia , Neoplasias del Plexo Coroideo/patología , Neoplasias del Plexo Coroideo/terapia , Papiloma del Plexo Coroideo/patología , Papiloma del Plexo Coroideo/terapia , Adolescente , Adulto , Niño , Preescolar , Supervivencia sin Enfermedad , Femenino , Hospitales Universitarios , Humanos , Lactante , Estimación de Kaplan-Meier , Masculino , Persona de Mediana Edad , Papiloma del Plexo Coroideo/mortalidad , Estudios Retrospectivos , Resultado del Tratamiento , Adulto Joven
2.
Anticancer Res ; 35(5): 3013-7, 2015 May.
Artículo en Inglés | MEDLINE | ID: mdl-25964589

RESUMEN

BACKGROUND: Choroid plexus carcinomas (CPCs) are rare pediatric tumors often associated with Li-Fraumeni Syndrome (LFS), a germline mutation in the TP53 tumor-suppressor gene, predisposing to cancer. MATERIALS AND METHODS: We performed a systemic literature review from 1990-2013 to evaluate the hypothesis that radiation therapy should be avoided in patients with CPC and LFS. Overall survival (OS) was compared using Kaplan-Meier curves and log-rank tests. RESULTS: Twenty-eight patients were documented with CPC and LFS. Eleven out of 17 patients received radiation therapy. The survival of patients receiving radiation was inferior to that of those without radiation [median (±95% confidence interval) 2-year OS=0.18 ± 0.12% versus 0.58 ± 0.12%]. The log-rank tests suggested the difference to be marginally significant (p=0.056). CONCLUSION: This finding provides evidence for pursuing treatment approaches that do not include radiation therapy for patients with LFS.


Asunto(s)
Carcinoma/radioterapia , Neoplasias del Plexo Coroideo/radioterapia , Síndrome de Li-Fraumeni/radioterapia , Proteína p53 Supresora de Tumor/genética , Carcinoma/complicaciones , Carcinoma/patología , Niño , Preescolar , Neoplasias del Plexo Coroideo/complicaciones , Neoplasias del Plexo Coroideo/patología , Femenino , Predisposición Genética a la Enfermedad , Mutación de Línea Germinal , Humanos , Lactante , Estimación de Kaplan-Meier , Síndrome de Li-Fraumeni/complicaciones , Síndrome de Li-Fraumeni/patología , Masculino
3.
Psychol Sci ; 18(12): 1040-3, 2007 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-18031409

RESUMEN

Does encountering information-processing conflict recruit general mechanisms of cognitive control or change only the representations of specific cues and responses? In the present experiments, a flanker task elicited responses to symbolic information (arrow meaning), whereas Stroop-like tasks elicited responses to nonsymbolic information (color of a letter or location of a target box). Despite these differences, when participants performed the flanker and Stroop tasks intermittently in randomized orders, the extent of information-processing conflict encountered on a particular trial modulated performance on the following trial. On across-task trial pairs, increases in response time to incongruent relative to congruent stimulus arrays were smaller immediately following incongruent trials than immediately following congruent trials. The degree of cognitive control exerted on a particular task thus appears to reflect not only the quality, but also the quantity, of recent experiences of information-processing conflict.


Asunto(s)
Cognición , Tiempo de Reacción , Ajuste Social , Adulto , Señales (Psicología) , Femenino , Humanos , Masculino , Programas Informáticos , Simbolismo
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