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1.
J Craniofac Surg ; 24(2): 523-5, 2013 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-23524732

RESUMEN

BACKGROUND: Malignant rhabdoid tumors are rare and aggressive tumors of pediatric age. The primary tumor can occur in different localizations, but it mainly involves kidney, soft tissue, or central nervous system. It has been associated to a poor diagnosis. METHODS: The authors present the case of a 10-day-old newborn affected by a bulky nasofronto-orbitary neoplasm. The patient underwent radical surgical treatment and further excision of a preauricular metastasis combined with postoperative chemotherapy treatment. RESULTS: The authors adopted a diagnostic and therapeutic protocol according to international guidelines, not without difficulty because the first histological report showed esthesioneuroblastoma. The rarity and aggresivity of rhabdoid tumor and the precocity of onset in our patient presented a difficulty to define prognostic factors and survival rates, as well as therapeutic plan of treatment. CONCLUSIONS: The authors underline the importance of a correct prenatal diagnosis and an early surgical treatment to reach the complete healing of the patient.


Asunto(s)
Neoplasias de Cabeza y Cuello/cirugía , Tumor Rabdoide/cirugía , Neoplasias de Cabeza y Cuello/diagnóstico , Humanos , Recién Nacido , Imagen por Resonancia Magnética , Masculino , Diagnóstico Prenatal , Tumor Rabdoide/diagnóstico , Tomografía Computarizada por Rayos X
2.
Eur J Paediatr Neurol ; 12(3): 183-9, 2008 May.
Artículo en Inglés | MEDLINE | ID: mdl-17881261

RESUMEN

OBJECTIVE: To evaluate the possible additional benefit in terms of prognostic accuracy of an integrated application of a traditional scorable method of neurologic examination and the Prechtl's method of qualitative assessment of general movements (GMs) in a large population of 903 consecutive preterm infants. STUDY DESIGN: Infants were enrolled from the Intensive Care Unit of the University of Catania. Inclusion criteria were a gestational age below 37 weeks and the absence of genetic disorders. All infants underwent serial ultrasound and at 3 months performed both the GMs assessment and the Hammersmith Infant Neurologic Examination (HINE). Outcome was assessed at 2 years by the Touwen neurologic examination and the Clinical Adaptive Test/Clinical, Linguistic and Auditory Milestone Scale. RESULTS: The integration of the two methods was shown to be more effective than the single assessments in predicting neurologic outcome. The additional benefit of combining the two approaches was particularly clear for the discrimination between unilateral and bilateral cerebral palsy. CONCLUSIONS: The integrated use of a scorable neurological examination and Prechtl's assessment of GMs can improve early prediction of neurodevelopmental outcome in preterm infants and should complement other clinical and instrumental exams in follow-up programs.


Asunto(s)
Recien Nacido Prematuro/fisiología , Examen Neurológico/métodos , Observación , Trastornos Psicomotores/diagnóstico , Humanos , Lactante , Recién Nacido , Movimiento/fisiología , Observación/métodos , Grabación de Cinta de Video
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