Submitted by jec3011 on March 17, 2023 - 5:31pm
Title | Primary leptomeningeal primitive neuroectodermal tumor. |
Publication Type | Journal Article |
Year of Publication | 2003 |
Authors | Begemann M, Lyden D, Rosenblum MK, Lis E, Wolden S, Antunes NL, Dunkel IJ |
Journal | J Neurooncol |
Volume | 63 |
Issue | 3 |
Pagination | 299-303 |
Date Published | 2003 Jul |
ISSN | 0167-594X |
Keywords | Antineoplastic Combined Chemotherapy Protocols, Carboplatin, Child, Combined Modality Therapy, Cranial Irradiation, Cyclophosphamide, Fatal Outcome, Humans, Lomustine, Magnetic Resonance Imaging, Male, Meningeal Neoplasms, Neuroectodermal Tumors, Primitive, Radiotherapy Dosage, Remission Induction, Vincristine |
Abstract | Leptomeningeal metastases are a common complication of medulloblastomas and other primitive neuroectodermal tumors (PNETs). Much rarer are PNETs apparently arising in the leptomeninges. An 8-year-old boy presented with headache and vomiting, due to neoplastic meningitis from primary neuroectodermal tumor without an identifying mass. After craniospinal irradiation and chemotherapy (carboplatin, vincristine, cyclophosphamide and lomustine) the boy was in remission for 14 months, then suffered several relapses despite various chemotherapy regimens. After the initial presentation of 3.5 years the boy began to suffer from prolonged refractory non-convulsive status epilepticus and later expired from progression of primary leptomeningeal PNET. |
DOI | 10.1023/a:1024324700411 |
Alternate Journal | J Neurooncol |
PubMed ID | 12892237 |