Malignant pediatric brain tumor of primitive small round cell proliferation with bland-looking mesenchymal spindle cell elements

Akira Ito, Toshihiro Kumabe, Ryuta Saito, Yukihiko Sonoda, Mika Watanabe, Yoichi Nakazato, Teiji Tominaga

研究成果: Article査読

4 被引用数 (Scopus)

抄録

It is often difficult to classify rare malignant pediatric mixed brain tumors composed of mesenchymal elements. A 6-year-old boy presented to our hospital with a left frontal massive tumor manifesting as complaints of rapidly progressive right hemiparesis and motor aphasia over 2 weeks. Computed tomography showed a left frontal mass with thick calcification. Magnetic resonance imaging revealed an enhanced lesion with perifocal edema and mass effect. Total removal of the tumor was performed. Histological examination of the resected tumor revealed an anaplastic malignant small round cell component with a bland-looking mesenchymal spindle cell component. The patient was treated with irradiation to the whole craniospinal axis and a boost to the tumor bed, followed by chemotherapy consisting of ifosfamide, cisplatin, and etoposide, resulting in good control without local recurrence or metastasis at 2 years. A combined malignant tumor composed of ectodermal and mesenchymal components is generally named malignant ectomesenchymoma (MEM). The more malignant part of MEM is the mesenchymalcomponent in most cases. In the present case, the moremalignant component was not the mesenchymal component, but the small round cells.

本文言語English
ページ(範囲)109-116
ページ数8
ジャーナルBrain Tumor Pathology
30
2
DOI
出版ステータスPublished - 2013 4

ASJC Scopus subject areas

  • 腫瘍学
  • 臨床神経学
  • 癌研究

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