| Literature DB >> 21494368 |
Sang-Deok Kim1, Tae-Young Jung, Shin Jung, Hee-Jo Baek.
Abstract
Neuroblastoma is a common tumor of children. We report a patient with extensive calvarial metastases of a neuroblastoma as an initial presentation. A 2-year-old girl presented with a history of gradually increasing head size and fever. A brain CT showed a multilobulated, large, extra-axial tumor involving both frontotemporoparietal areas with a sunray-spiculated hyperostosis of the skull and marked contrast enhancement. A brain MRI demonstrated extensive calvarial lesions with simultaneous involvement of the orbits. A biopsy was performed and a ganglioneuroblastoma was diagnosed. On systemic evaluation, an enlarged abdominal mass was detected. After neo-adjuvant chemotherapy, most of the tumors disappeared except for a tumor in the left parietal area; there was a corresponding decrease in the circumference of the head. We performed surgery for the remnant mass. Intensive chemotherapy was administered and a bone marrow transplantation was performed. Adequate neo-adjuvant chemotherapy followed by surgery to the neuroblatoma with extensive metastases to the skull and orbit may be helpful.Entities:
Keywords: Calvarium; Chemotherapy; Metastasis; Neuroblastoma
Year: 2011 PMID: 21494368 PMCID: PMC3070900 DOI: 10.3340/jkns.2011.49.1.68
Source DB: PubMed Journal: J Korean Neurosurg Soc ISSN: 1225-8245