Primary leptomeningeal primitive neuroectodermal tumor.

TitlePrimary leptomeningeal primitive neuroectodermal tumor.
Publication TypeJournal Article
Year of Publication2003
AuthorsBegemann M, Lyden D, Rosenblum MK, Lis E, Wolden S, Antunes NL, Dunkel IJ
JournalJ Neurooncol
Volume63
Issue3
Pagination299-303
Date Published2003 Jul
ISSN0167-594X
KeywordsAntineoplastic 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.

DOI10.1023/a:1024324700411
Alternate JournalJ Neurooncol
PubMed ID12892237