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Pineal teratoma with nephroblastic component in a newborn male: Case report and review of the literature.
Thoe, Jessica; Ducis, Katrina; Eldomery, Mohammad K; Marshall, Mark; Ferguson, Michael; Vortmeyer, Alexander O; Raskin, Jeffrey S; Coven, Scott L.
Afiliación
  • Thoe J; Section of Pediatric Hematology/Oncology, Riley Hospital for Children, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA. Electronic address: jthoe@iu.edu.
  • Ducis K; Section of Pediatric Neurosurgery, Riley Hospital for Children, Department of Neurological Surgery, Indiana University School of Medicine, Indianapolis, IN, USA. Electronic address: kducis@iuhealth.org.
  • Eldomery MK; Department of Pathology, Indiana University School of Medicine, Indianapolis, IN, USA. Electronic address: meldomer@iupui.edu.
  • Marshall M; Department of Precision Medicine, Riley Hospital for Children, Indiana University School of Medicine, Indianapolis, IN, USA. Electronic address: mmarsha@iu.edu.
  • Ferguson M; Section of Pediatric Hematology/Oncology, Riley Hospital for Children, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA. Electronic address: micjferg@iu.edu.
  • Vortmeyer AO; Department of Pathology, Indiana University School of Medicine, Indianapolis, IN, USA. Electronic address: avortmeyer@iu.edu.
  • Raskin JS; Section of Pediatric Neurosurgery, Riley Hospital for Children, Department of Neurological Surgery, Indiana University School of Medicine, Indianapolis, IN, USA. Electronic address: jraskin@iuhealth.org.
  • Coven SL; Section of Pediatric Hematology/Oncology, Riley Hospital for Children, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA. Electronic address: scoven@iu.edu.
J Clin Neurosci ; 80: 207-214, 2020 Oct.
Article en En | MEDLINE | ID: mdl-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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pinealoma / Teratoma / Neoplasias Complejas y Mixtas / Tumor de Wilms Límite: Humans / Male / Newborn Idioma: En Revista: J Clin Neurosci Asunto de la revista: NEUROLOGIA Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Pinealoma / Teratoma / Neoplasias Complejas y Mixtas / Tumor de Wilms Límite: Humans / Male / Newborn Idioma: En Revista: J Clin Neurosci Asunto de la revista: NEUROLOGIA Año: 2020 Tipo del documento: Article