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Pediatric cerebral ganglioneuroblastoma.

Abstract

We describe a 4-year-old girl with acute onset headaches and transient blindness who underwent surgical intervention, chemotherapy, and radiotherapy for an intracranial mass. This mass was pathologically confirmed as a primary intracranial ganglioneuroblastoma, a rare finding in the pediatric population. The literature on pediatric primary intracranial ganglioneuroblastoma is reviewed.

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  • Authors+Show Affiliations

    ,

    Cleveland Clinic Lerner College of Medicine and Department of Pathology, L25 9500 Euclid Avenue, Cleveland, OH 44195, USA.

    Cleveland Clinic Lerner College of Medicine and Department of Pathology, L25 9500 Euclid Avenue, Cleveland, OH 44195, USA. Electronic address: praysor@ccf.org.

    Source

    MeSH

    Antineoplastic Combined Chemotherapy Protocols
    Brain Neoplasms
    Chemotherapy, Adjuvant
    Child, Preschool
    Female
    Ganglioneuroblastoma
    Hemianopsia
    Humans
    Neurosurgical Procedures
    Radiotherapy, Adjuvant
    Seizures
    Treatment Outcome

    Pub Type(s)

    Case Reports
    Journal Article

    Language

    eng

    PubMed ID

    25216629

    Citation

    * When formatting your citation, note that all book, journal, and database titles should be italicized* Article titles in AMA citation format should be in sentence-case
    TY - JOUR T1 - Pediatric cerebral ganglioneuroblastoma. AU - Steenberge,Sean P, AU - Prayson,Richard A, Y1 - 2014/09/10/ PY - 2014/07/15/received PY - 2014/07/28/accepted PY - 2014/9/14/entrez PY - 2014/9/14/pubmed PY - 2016/2/5/medline KW - Brain tumor KW - Ganglioneuroblastoma KW - Pediatric brain tumor KW - Primitive neuroectodermal tumor SP - 2023 EP - 5 JF - Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia JO - J Clin Neurosci VL - 21 IS - 11 N2 - We describe a 4-year-old girl with acute onset headaches and transient blindness who underwent surgical intervention, chemotherapy, and radiotherapy for an intracranial mass. This mass was pathologically confirmed as a primary intracranial ganglioneuroblastoma, a rare finding in the pediatric population. The literature on pediatric primary intracranial ganglioneuroblastoma is reviewed. SN - 1532-2653 UR - https://www.unboundmedicine.com/medline/citation/25216629/Pediatric_cerebral_ganglioneuroblastoma_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0967-5868(14)00496-2 DB - PRIME DP - Unbound Medicine ER -