Disseminated Cerebrospinal Embryonal Tumor in the Adult.
Alessandro CaporlinguaDaniele ArmocidaFederico CaporlinguaGennaro LapadulaGrazia Maria ElefanteManila AntonelliMaurizio SalvatiPublished in: Case reports in pathology (2016)
Introduction. According to the 2016 World Health Organization classification of Tumors of the Central Nervous System, the term Primitive Neuroectodermal Tumor has been replaced by the term Embryonal Tumor (ET). We present a case of disseminated cerebrospinal ET presenting in an adult patient. Illustrative Case. A 49-year-old male presenting with low back pain, dysuria, and hypoesthesia of the lower extremities referred to our emergency department. Brain and whole spine contrast-enhanced MRI documented a diffusively disseminated heterogeneous neoplasm with intradural extra- and intramedullary involvement of the cervicothoracic tract and cauda equina. A primary biopsy of the lumbosacral localization was performed through L5 bilateral laminectomy. Histologic diagnosis was Embryonal Tumor Not Otherwise Specified. The patient underwent chemotherapy with postoperative adjuvant alternating Vincristine-Doxorubicin-Ifosfamide (VAI) and Ifosfamide-Etoposide (IE). Discussion. Spinal ETs are exceedingly rare especially when presenting in the adult patient. Neurosurgical and oncologic management is still unclear. When feasible, surgical removal should always be performed to obtain a histologic diagnosis. Postoperative adjuvant therapy might entail both chemo- and radiotherapy; however a consensus on this matter is still lacking.
Keyphrases
- case report
- contrast enhanced
- emergency department
- magnetic resonance imaging
- early stage
- locally advanced
- preterm infants
- diffusion weighted imaging
- magnetic resonance
- patients undergoing
- diffusion weighted
- computed tomography
- radiation therapy
- machine learning
- spinal cord
- prostate cancer
- squamous cell carcinoma
- cerebrospinal fluid
- brain injury
- minimally invasive
- functional connectivity