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1.
Pediatr Blood Cancer ; 62(3): 529-30, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25611048

RESUMO

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.


Assuntos
Neoplasias Ósseas/terapia , Osteossarcoma/terapia , Prevenção Secundária/métodos , Protocolos de Quimioterapia Combinada Antineoplásica/administração & dosagem , Neoplasias Ósseas/patologia , Criança , Humanos , Masculino , Recidiva Local de Neoplasia , Osteossarcoma/patologia
2.
Pediatr Blood Cancer ; 48(1): 50-6, 2007 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-16470521

RESUMO

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.


Assuntos
Doenças do Sistema Nervoso Central/etiologia , Diabetes Insípido Neurogênico/etiologia , Histiocitose de Células de Langerhans/complicações , Doenças da Hipófise/etiologia , Adolescente , Adulto , Sistema Nervoso Central/patologia , Doenças do Sistema Nervoso Central/mortalidade , Doenças do Sistema Nervoso Central/patologia , Criança , Pré-Escolar , Diabetes Insípido Neurogênico/mortalidade , Diabetes Insípido Neurogênico/patologia , Feminino , Seguimentos , Histiocitose de Células de Langerhans/mortalidade , Histiocitose de Células de Langerhans/patologia , Humanos , Lactente , Masculino , Monitorização Fisiológica , Doenças da Hipófise/mortalidade , Doenças da Hipófise/patologia
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