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Pineal teratoma with nephroblastic component in a newborn male: Case report and review of the literature.

作者信息

Thoe Jessica, Ducis Katrina, Eldomery Mohammad K, Marshall Mark, Ferguson Michael, Vortmeyer Alexander O, Raskin Jeffrey S, Coven Scott L

机构信息

Section of Pediatric Hematology/Oncology, Riley Hospital for Children, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.

Section of Pediatric Neurosurgery, Riley Hospital for Children, Department of Neurological Surgery, Indiana University School of Medicine, Indianapolis, IN, USA.

出版信息

J Clin Neurosci. 2020 Oct;80:207-214. doi: 10.1016/j.jocn.2020.07.044. Epub 2020 Aug 27.

DOI:10.1016/j.jocn.2020.07.044
PMID:33099347
Abstract

Neonatal germ cell tumors are rare and comprise both benign and malignant neoplasms. Teratoma with nephroblastoma is a malignant subset defined pathologically by the presence of nephroblastoma and teratoma elements. Although teratoma with nephroblastoma is most often found in the kidney, 24 of 59 reported cases are associated with extrarenal locations, such as the mediastinum or retroperitoneum. To our knowledge, this is the first patient in the literature with intracranial/pineal teratoma with nephroblastoma, which was managed with staged transcranial approaches resulting in gross total resection and no adjuvant therapy (surveillance observation imaging). We further augmented the patient's management by comprehensive genomic profiling of the tumor to better understand the molecular biology and explore options for targeted therapy.

摘要

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