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J Pediatr Hematol Oncol ; 44(7): 415-418, 2022 10 01.
Artículo en Inglés | MEDLINE | ID: mdl-35704799

RESUMEN

Medulloblastoma has a reduced incidence in Down syndrome (DS). This protective characteristic has not been clarified yet. Here, we report the second case of SHH medulloblastoma and DS documented in the literature. A complete surgery was performed followed by reduced craniospinal irradiation dose and adjuvant chemotherapy. No evidence of tumor recurrence was observed. The overall survival was 9.1 years. No family history or physical stigma of other hereditary predisposition syndrome was found. In the elucidation of this extremely rare association, future case reports play an important role in defining the spectrum of brain tumors and their peculiar features in DS.


Asunto(s)
Neoplasias Cerebelosas , Irradiación Craneoespinal , Síndrome de Down , Meduloblastoma , Neoplasias Cerebelosas/tratamiento farmacológico , Síndrome de Down/complicaciones , Humanos , Meduloblastoma/patología , Recurrencia Local de Neoplasia
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