Successful Multimodal Treatment of Intracranial Growing Teratoma Syndrome with Malignant Features
Molecular analysis of the growing teratoma syndrome has not been extensively studied. Here, we report a 14-year-old boy with a growing mass during treatment for a mixed germ cell tumor of the pineal region. Tumor markers were negative; thus, growing teratoma syndrome was suspected. A radical resecti...
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Veröffentlicht in: | Current oncology (Toronto) 2024-04, Vol.31 (4), p.1831-1838 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Molecular analysis of the growing teratoma syndrome has not been extensively studied. Here, we report a 14-year-old boy with a growing mass during treatment for a mixed germ cell tumor of the pineal region. Tumor markers were negative; thus, growing teratoma syndrome was suspected. A radical resection via the occipital transtentorial approach was performed, and histopathological examination revealed a teratoma with malignant features. Methylation classifier analysis confirmed the diagnosis of teratoma, and
loss and 12p gain were identified by copy number variation analysis, potentially elucidating the cause of growth and malignant transformation of the teratoma. The patient remains in remission after intense chemoradiation treatment as a high-risk germ cell tumor. |
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ISSN: | 1718-7729 1198-0052 1718-7729 |
DOI: | 10.3390/curroncol31040138 |