Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Más filtros










Base de datos
Intervalo de año de publicación
1.
Pediatr Blood Cancer ; 62(3): 529-30, 2015 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-25611048

RESUMEN

The prognosis after relapse of high-grade osteosarcoma is poor and complete resection of all tumors is essential for survival. A 6-year old was diagnosed with high-grade osteosarcoma and treated according to the COSS-96 protocol. Within 5 years from initial diagnosis, five osteosarcoma relapses occurred and every time it was possible to achieve complete surgical remission. Additional treatments included chemotherapy and dendritic cell-based cancer immune therapy. Since the end of therapy of the 5th relapse, he is alive for 11½ years. Our experience further supports that aggressive surgery can help to achieve long-term survival even in patients with multiple osteosarcoma relapses.


Asunto(s)
Neoplasias Óseas/terapia , Osteosarcoma/terapia , Prevención Secundaria/métodos , Protocolos de Quimioterapia Combinada Antineoplásica/administración & dosificación , Neoplasias Óseas/patología , Niño , Humanos , Masculino , Recurrencia Local de Neoplasia , Osteosarcoma/patología
2.
Pediatr Blood Cancer ; 48(1): 50-6, 2007 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-16470521

RESUMEN

BACKGROUND: Permanent consequences in Langerhans cell histiocytosis (LCH) are irreversible late sequelae related to the disease that may severely impair the quality of life of survivors. The frequency and pattern of permanent consequences affecting the central nervous system (CNS) remains to be determined. PROCEDURE: In this single center study, 25 LCH patients observed for a median time of 10 years 3 months underwent a uniform thorough follow-up program including neuropsychological testing and electrophysiological evaluation. RESULTS: Overall permanent consequences were seen in 9 of 25 patients. Intracranial abnormalities were the most frequent including diabetes insipidus (DI) in seven patients, anterior pituitary deficiencies in five patients, and neurodegenerative CNS disease in five patients. No patient had overt neurological symptoms upon neurological evaluation, but psychological testing revealed subtle deficits in short-term auditory memory (STAM) in 14 patients. Brain stem evoked potentials showed abnormalities in four of nine tested patients, all of these four had neurodegeneration on MRI. CONCLUSION: Psychoneuroendocrine sequelae were found in an unexpectedly high number of patients in this single center study. Long-term follow-up focusing on such sequelae are important in LCH survivors, in order to detect early deficits, to monitor the evolution of the disease, and to provide specific support.


Asunto(s)
Enfermedades del Sistema Nervioso Central/etiología , Diabetes Insípida Neurogénica/etiología , Histiocitosis de Células de Langerhans/complicaciones , Enfermedades de la Hipófisis/etiología , Adolescente , Adulto , Sistema Nervioso Central/patología , Enfermedades del Sistema Nervioso Central/mortalidad , Enfermedades del Sistema Nervioso Central/patología , Niño , Preescolar , Diabetes Insípida Neurogénica/mortalidad , Diabetes Insípida Neurogénica/patología , Femenino , Estudios de Seguimiento , Histiocitosis de Células de Langerhans/mortalidad , Histiocitosis de Células de Langerhans/patología , Humanos , Lactante , Masculino , Monitoreo Fisiológico , Enfermedades de la Hipófisis/mortalidad , Enfermedades de la Hipófisis/patología
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA