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Authordc.contributor.authorTrincado M., Arturo 
Authordc.contributor.authorLópez G., Juan Pablo es_CL
Authordc.contributor.authorGonzález N., Militza es_CL
Authordc.contributor.authorVillaseca D., Eduardo es_CL
Authordc.contributor.authorRoizen B., Alejandra es_CL
Authordc.contributor.authorManieu M., Denise es_CL
Authordc.contributor.authorDíaz C., José es_CL
Authordc.contributor.authorVillarroel C., Milena es_CL
Authordc.contributor.authorHenríquez V., Alejandra es_CL
Authordc.contributor.authorLatorre L., Juan José es_CL
Authordc.contributor.authorGalano Triviño, Sergio es_CL
Admission datedc.date.accessioned2010-04-05T20:04:37Z
Available datedc.date.available2010-04-05T20:04:37Z
Publication datedc.date.issued2008-12
Cita de ítemdc.identifier.citationRevista Chilena de Pediatría - Noviembre/Diciembre 2008; 79 (6): 614-622en_US
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/128428
Abstractdc.description.abstractRetrospective analysis of clinical charts of 41 children (59 eyes) diagnosed with retinoblastoma and treated by a multidisciplinary team at Hospital Luis Calvo Mackenna in Santiago-Chile, between 1999 and 2007. The information included gender, laterality, diagnosis age, presenting signs, tumor spread, treatment modality and survival rate. Results: A total of 23 cases (56%) were unilateral and 18 cases (44%) were bilateral. The mean age at diagnosis was 21.6 months (range 2 - 84) and 27 children (65.9%) were male. The most common presenting signs were leucokoria (51.2%), strabismus (24.4%) and proptosis (4.9%). Enucleation was performed in 48 eyes (81.3%), being the only required treatment in 17 children (41.5%). The remaining 24 patients received systemic and/or local therapy with chemotherapy, focal therapy and external beam radiation. 5 children died during the follow - up study period, due to extraocular extension to the orbit, central nervous system and bone marrow. Conclusion: In spite of high enucleation rate as initial therapy for retinoblastoma, the survival rate with this current treatment protocol is similar to those from developed countries.en_US
Lenguagedc.language.isoesen_US
Keywordsdc.subjectRetinoblastomaen_US
Títulodc.titleRetinoblastoma en pediatría, experiencia en un hospital pediátricoen_US
Title in another languagedc.title.alternativeRetinoblastoma in children, experience at a pediatric hospitalen_US
Document typedc.typeArtículo de revista


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